Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Latent class analysis of barriers to HIV testing services and associations with sexual behaviour and HIV status among adolescents and young adults in Nigeria

  • Okikiolu Badejo ,

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Writing – original draft, Writing – review & editing

    Okikolubadejo@gmail.com

    Affiliations Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium, Department of Sociology, University of Antwerp, Antwerp, Belgium, APIN Public Health Institute, Abuja, Nigeria

  • Edwin Wouters,

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Project administration, Writing – review & editing

    Affiliation Department of Sociology, University of Antwerp, Antwerp, Belgium

  • Sara Van Belle,

    Roles Funding acquisition, Investigation, Supervision, Validation, Writing – review & editing

    Affiliation Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium

  • Anne Buve,

    Roles Conceptualization, Formal analysis, Supervision, Writing – review & editing

    Affiliation Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium

  • Tom Smekens,

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Writing – review & editing

    Affiliation Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium

  • Plang Jwanle,

    Roles Conceptualization, Project administration, Writing – review & editing

    Affiliation APIN Public Health Institute, Abuja, Nigeria

  • Marie Laga,

    Roles Funding acquisition, Project administration, Writing – review & editing

    Affiliation Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium

  • Christiana Nöstlinger

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Project administration, Supervision, Validation, Writing – review & editing

    Affiliation Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium

Abstract

Introduction

Adolescents and young adults (AYA) face multiple barriers to accessing healthcare services, which can interact, creating complex needs that often impact health behaviours, leading to increased vulnerability to HIV. We aimed to identify distinct AYA subgroups based on patterns of barriers to HIV testing services and assess the association between these barrier patterns and sexual behaviour, socio-demographics, and HIV status.

Methods

Data were from Nigeria’s AIDS Indicator and Impact Survey (NAIIS, 2018) and included 18,612 sexually active AYA aged 15–24 years who had never been tested for HIV and reported barriers to accessing HIV testing services. A Latent class analysis (LCA) model was built from 12 self-reported barrier types to identify distinct subgroups of AYA based on barrier patterns. Latent class regressions (LCR) were conducted to compare the socio-demographics, sexual behaviour, and HIV status across identified AYA subgroups. Sex behaviour characteristics include intergenerational sex, transactional sex, multiple sex partners, condom use, and knowledge of partner’s HIV status.

Results

Our LCA model identified four distinct AYA subgroups termed ’low-risk perception’ (n = 7,361; 39.5%), ’consent and proximity’ (n = 5,163; 27.74%), ’testing site’ (n = 4,996; 26.84%), and ’cost and logistics’ (n = 1,092; 5.87%). Compared to adolescents and young adults (AYA) in the low-risk perception class, those in the consent and proximity class were more likely to report engaging in intergenerational sex (aOR 1.17, 95% CI 1.02–1.35), transactional sex (aOR 1.50, 95% CI 1.23–1.84), and have multiple sex partners (aOR 1.75, 95% CI 1.39–2.20), while being less likely to report condom use (aOR 0.79, 95% CI 0.63–0.99). AYA in the testing site class were more likely to report intergenerational sex (aOR 1.21, 95% CI 1.04–1.39) and transactional sex (aOR 1.53, 95% CI 1.26–1.85). AYA in the cost and logistics class were more likely to engage in transactional sex (aOR 2.12, 95% CI 1.58–2.84) and less likely to report condom use (aOR 0.58, 95% CI 0.34–0.98). There was no significant relationship between barrier subgroup membership and HIV status. However, being female, aged 15–24 years, married or cohabiting, residing in the Southsouth zone, and of Christian religion increased the likelihood of being HIV infected.

Conclusions

Patterns of barriers to HIV testing are linked with differences in sexual behaviour and sociodemographic profiles among AYA, with the latter driving differences in HIV status. Findings can improve combination healthcare packages aimed at simultaneously addressing multiple barriers and determinants of vulnerability to HIV among AYA.

Introduction

The global goal to end the AIDS epidemic by 2030 requires expanded HIV prevention and treatment interventions, making them accessible to all in need [1, 2]. However, adolescents and young adults (AYA), particularly in low and middle-income countries, face challenges in progressing toward this goal [3]. These challenges have led to significant disparities in achieving the global 95-95-95 targets for HIV elimination [1, 4]. The 95-95-95 targets are a set of global goals for HIV prevention and treatment that were set by the Joint United Nations Programme on HIV/AIDS (UNAIDS) in 2020. The goals are aimed for 95% of all people living with HIV to know their HIV status, 95% of all people with diagnosed HIV infection to receive sustained antiretroviral therapy, and 95% of all people receiving antiretroviral therapy to have viral suppression by 2025 [1]. As of 2020, treatment coverage among young adults living with HIV aged 15–24 was estimated at 55%, significantly lower than the 75% coverage among those over 25 years [1]. In 2019, the number of new HIV infections among adolescents and young adults aged 15 to 24 decreased to an estimated 460,000 new infections, representing a 46% decline since the year 2000. However, this is still eight times higher than the global target of fewer than 50,000 new infections by 2025 [5, 6]. Remarkably, over 80% of these new infections occurred in sub-Saharan Africa [5]. Nigeria, one of the countries with the highest burdens of adolescents living with HIV (ALHIV) in sub-Saharan Africa, continues to experience increases in mortality among both younger and older adolescents in contrast to other countries in the region [7, 8]. In addition, only 31% of young people aged 15–24 in Nigeria are aware of their HIV status, significantly below the national average of 46.9% [9].

The slower progress in AYA HIV-related outcomes is linked to health services’ inability to address young peoples’ multiple and complex needs [10, 11]. These needs encompass a range of services and are compounded by multiple barriers to access [10, 11]. These barriers include financial, social (such as stigma), and informational obstacles [12, 13]. In Nigeria, there is a noticeable lack of services related to mental health, reproductive health, clinic transitional care, and psychosocial support for young people living with HIV which might explain the poor health-seeking behaviour and heightened vulnerability to HIV observed in this age group [1420]. Despite the need for comprehensive and integrated approaches to address these multifaceted needs, healthcare services often fall short due to fragmented and siloed care provision which presents multiple barriers to access [12]. Recognising this challenge, there has been a growing trend toward bundled healthcare interventions [21, 22] that combine various services and support to comprehensively and simultaneously address young people’s multiple barriers and needs. One such combination of health service interventions in Nigeria is the "Minimum package for Youth-friendly services" targeting young people [23]. While bundled healthcare interventions are considered effective when they simultaneously address social, behavioural and structural barriers, their outcomes in practice have been mixed [1926]. To enhance their effectiveness, a more targeted and holistic approach that aligns with specific patterns of barrier combinations faced by young people with diverse challenges is needed [1926].

To address this need, this study utilises Latent Class Analysis (LCA) to model barrier patterns related to HIV testing services among AYA in Nigeria. LCA is a statistical modelling technique that identifies distinct subgroups (latent classes) within a population based on shared patterns of specific characteristics [26]. It classifies individuals into unobserved subgroups, estimating these based on multivariate clustering of observed variables to account for population heterogeneity [27, 28]. The number of subgroups in LCA is not determined a priori; instead, it is selected based on a combination of different model-fit criteria. LCA offers several advantages over similar cluster analysis techniques, such as k-means. It relies more on formal criteria to determine the final model and is flexible in accommodating different variable scales [26]. Furthermore, LCA addresses some methodological challenges encountered in traditional subgroup analysis, such as high type 1 error, low statistical power, issues related to collinearity, and difficulties analysing and modelling complex and multidimensional interactions between observed variables [26, 29, 30]. LCA can be extended by incorporating external covariates and outcomes to enhance understanding of the relationships between latent classes and external variables [31]. This is achieved through Latent class regression (LCR), where external covariates or outcomes are regressed on latent classes or subgroups [32]. LCA has been previously employed in studies focused on sexual health and HIV in young people, as well as barriers to health services [19, 3335]. However, to the best of our knowledge, the application of LCA and LCR to investigate association between barriers to HIV testing services, sexual behaviour and HIV status in young people has not been previously explored. This study builds upon previous studies in Nigeria investigating the relationship between the utilisation of HIV testing and prevention services, sexual behaviour and vulnerability to HIV in AYA in Nigeria [3638].

Our study aims to: identify latent classes of AYA based on shared patterns of barriers to HIV testing services using LCA, identify and compare the sexual and sociodemographic characteristics of AYA across different latent classes using LCR, and explore the association between latent class membership of AYA and observed HIV status using LCR, adjusting for sexual and sociodemographic characteristics.

Method

Context

Nigeria is administratively divided into six geopolitical zones (Northwest, Northeast, Northcentral, Southwest, Southeast, and Southsouth) comprising 36 states and one Federal capital (Fig 1). Despite economic growth in recent decades, the country continues to face high poverty rates [39]. Regional disparities are significant, with poverty levels ranging from 30% in the South to over 60% in the North [39]. Certain regions in the North have poverty rates exceeding 80% as of 2020 [39]. These disparities extend to health and education indices.

thumbnail
Fig 1. Map of Nigeria by zones.

Map data available from ©OpenStreetMap under the Open Database License.

https://doi.org/10.1371/journal.pone.0300220.g001

Women in the North have lower educational attainment, with average years of formal education reaching less than half of that in the South [39]. Similarly, households in the North are less asset-wealthy and have experienced increasing poverty compared to households in the South [39]. Maternal healthcare utilisation has been consistently lowest in the Northwest and Northeast regions and, together with the North Central, have the highest rates of child and under-five mortality [40, 41].

Data

This study used data from Nigeria’s National AIDS Indicator and Impact Survey (NAIIS). NAIIS was a nationally representative, cross-sectional, two-stage, population-based survey of households. NAIIS used a two-stage cluster sampling technique, selecting enumeration areas (EAs) followed by households. The sampling frame consisted of 662,855 EAs, 28,900,478 households and 140,431,798 persons based on the 2006 Census, with an average number of households and persons per EA of 44 and 212, respectively. The eligible survey population included adults aged 18–64 years, emancipated minors aged 15–17 years, children and adolescents aged 10–14 years, and children aged <10 years.

Participants’ recruitment, data and blood sample collection occurred from July 2018 to December 2018, focusing on HIV and related health indicators, including hepatitis B virus (HBV) infection, hepatitis C virus (HCV) infection, HBV/HIV co-infection and HCV/HIV co-infection [9]. For adults aged 15–64, the interview response rate was 91.6% for women and 88.2% for men; the blood draw response rate was 92.9% for women and 93.6% for men. For adolescents aged 10–14, the interview response rate was 86.8% for women and 86.2% for men, and the blood draw response rate was 91.2% for women and 92.3% for men. NAIIS is the first survey in Nigeria to estimate national HIV incidence and viral load suppression (VLS).

Three types of questionnaires were used: household questionnaire, adolescent questionnaire for individuals aged 10–14 years, and adult questionnaire for women and men aged 15 years or older. The adolescent and adult questionnaires collected information from eligible adolescents aged 10–14 years and adults aged 15 years and older on basic demographic characteristics, marriage, sexual activity, HIV and STI knowledge, attitudes and behaviours, and previous HIV testing. In addition to the interview, blood was drawn from consenting participants for HIV antibody testing. Final HIV status was determined using rapid HIV testing and Geenius™ HIV 1/2 confirmatory testing on all reactive rapid test results. The testing procedures and national testing algorithm used have been described elsewhere [9] and summarised in S1 File. Personal identifiers were excluded from the data set before analyses were performed. Details of the survey methods and questionnaire are available on the study website: https://nadanaiis.nascp.gov.ng/home.

Study participants

Our inclusion criteria, as illustrated in Fig 2, include adolescents (15–19 years) and young adults (20–24 years); being sexually active (that is, have had vaginal sex before the survey); never having been tested for HIV before the survey. We excluded participants who had missing information on the number of sexual partners.

thumbnail
Fig 2. Study flowchart showing inclusion and exclusion criteria.

https://doi.org/10.1371/journal.pone.0300220.g002

Measures

Study measures were based on the adult questionnaire. The questionnaire has ten modules focused on respondent consent and background and sociodemographic characteristics, marriage, reproduction, children, male circumcision, sexual activity, HIV testing, HIV care and treatment, tuberculosis and other health issues, and gender norms. Notably, NAIIS 2018 used only vaginal sex to determine being sexually active. We also retrieved the results of blood testing for HIV biomarkers. Details of the study measures are provided in Table 1.

Statistical analysis

For our first objective, we used LCA to identify latent classes or subgroups of AYA based on shared combination patterns of the 12 manifest barrier variables listed in Table 1, supported by the literature as relevant to HIV testing uptake in Nigeria and other settings [18, 36]. The LCA consisted of the following steps:

The first step included an iterative process of building models by gradually increasing the number of classes and employing various fit indicators to assess model fit. This method ensured the identification and selection of the model with the optimal number of classes. We used the following model fit indices to select the optimal model: Akaike Information Criteria (AIC), Bayesian Information Criteria (BIC), Entropy values and the Lo, Mendell and Rubin Likelihood Ratio Test (LMR). Smaller AIC and BIC values are preferable, while Entropy values should be close to 1 [26]. The LMR test indicates whether a model fits better than the model with one fewer class (the complex survey design did not permit using the Bootstrap Likelihood Ratio Test (BLRT)) [26, 30].

After selecting the model with the optimal number of classes, the next step involved assigning each AYA to a specific class. To achieve this, we employed the maximum probability rule, often referred to as the ’most likely class’ approach. In this approach, individuals are allocated to the class with their highest estimated probability [42]. Although an alternative method could involve assigning individuals to multiple classes based on their probabilities for each class, we opted for the most-likely class approach. This decision allowed us to examine variations in the frequencies of sociodemographic and sexual behavior characteristics among classes. This practice is considered acceptable, especially when entropy exceeds 0.80 [27].

Following class assignment, the subsequent step involved scrutinizing the conditional response probabilities for each barrier type within the identified classes. We applied labels to each class based on the HIV testing barrier(s) exhibiting higher conditional response probabilities. To address missing data, we employed the Mplus procedure of Bolck–Croon–Hagenaars (BCH) with multiple imputations on 20 data sets, accommodating the complexities of the survey design [28].

For the second objective, we used LCR with covariates [28, 43] to compare the sexual and sociodemographic characteristics of AYA across the different assigned latent classes or subgroups. The integrated 3-step approach in Mplus (R3STEP functionality) allowed us to compare these characteristics between classes while accounting for inherent potential classification errors in the most likely class approach [28, 43] as follows: (a) each AYA was first assigned using the most likely class approach, but their distributed probabilities across classes were computed and saved (b) We calculated the measurement error for each observation based on the probability used for its most likely class assignment and the probabilities distributed across different classes (c) In the regression model, we represent the latent class variable with the most likely class assignment and include pre-specified measurement errors obtained in step (b) [43]. We used the TYPE = COMPLEX MIXTURE feature to accommodate the complex survey nature of the dataset [28, 43]. To assess potential multicollinearity among the sexual and sociodemographic factors, we examined correlation matrices and calculated variance inflation factors (VIFs).

For our third objective, we used LCR with distal outcomes [28, 43] to explore the relationship between latent class membership of AYA and HIV positivity rates. We utilised Mplus’ automatic BCH regression procedure, which accounted for potential classification errors and accommodated the complex survey nature of the dataset [28, 44]. We then adjusted for sociodemographic and sexual characteristics in the model. We present crude and adjusted odds ratios and 95% confidence intervals (95% CI). Statistical significance was determined by the 95% CI of crude and adjusted odds ratios not overlapping 1.00 and, when indicated, p value less than 0.05.

To examine the consistency of our results, we conducted a sensitivity analysis using only complete cases from the non-imputed dataset. This analysis mirrored the key steps employed for the first and third objectives, specifically, using LCA to uncover latent classes or subgroups of AYA based on their shared patterns across the 12 barrier variables detailed in Table 1; and using LCR with distal outcomes to examine the relationship between latent class membership and HIV positivity rates, adjusting for sexual and sociodemographic factors.

We used STATA version 17.0 [45] to prepare the data, including cleaning and recoding variables and checking for missing data. The cleaned dataset was exported into Mplus version 8.8 for analysis [44].

Ethics approval and consent to participate

NAIIS 2018 had approval from the Nigeria National Health Research Ethics Committee and the IRBs of the US Center for Disease Control (CDC) University of Maryland Baltimore. All participants, per United States regulations, provided written and verbal informed consent or assent. For minors aged 10–17, written and verbal consent were obtained from parents or guardians for interviews and blood draws. Subsequently, assent was obtained from the minors.

Permission to access and use NAIIS 2018 data for this study was granted by a review committee established by the Nigeria Federal Ministry of Health. The broader study, which this study is a part of, also received ethical approvals from the Institute of Tropical Medicine, Belgium, and the APIN Public Health Initiatives, Nigeria. The approvals included waivers for secondary data analysis.

NAIIS2018 study data has been carefully anonymised to protect privacy, and we adhered to the terms and conditions outlined in the provided confidentiality agreement. Further information on the terms and conditions for NAIIS 2018 data access can be found at https://nadanaiis.nascp.gov.ng/home.

Result

We analysed 18,612 AYA who met the study inclusion criteria (Fig 2). Distribution of AYA by sociodemographic characteristics, sexual activity, barriers to HIV testing and HIV positivity rates is shown in S1 Table. Our LCA explored models with up to six classes, with model fit statistics shown in Table 2. A four-class model was selected as the best fit for the data based on the BIC and sample-size-adjusted BIC values. Although models with more latent classes were associated with lower AIC/BIC values, the drop in BIC plateaued after five classes, and the LMR tests indicated no significant improvement in fit (p = 0.1969). The selected model had a sufficient entropy of 0.873, indicating good class separation.

Table 3 presents the conditional response probabilities, and the class counts of AYA in the four classes based on the most likely class assignment. We labelled each class based on the barriers with higher conditional probabilities as follows: "Low-risk perception", "Consent and proximity", "Testing site", and "Cost and logistics". The class counts and proportions based on most-likely assignment are shown in Table 3. The class counts, and proportions based on distributed probabilities are available in S2 Table.

thumbnail
Table 3. Conditional response probabilities of barriers to HIV testing, with latent class proportion for each class reported as a percentage next to class name.

Figures in bold show probabilities > 0. 11, an arbitrary threshold selected to highlight the higher conditional response probabilities that informed the class labelling.; n is the final class count based on the most likely latent class.

https://doi.org/10.1371/journal.pone.0300220.t003

For the sensitivity analysis, our LCA explored models with up to seven classes, with model fit statistics shown in S2 File. Similar to result from imputed dataset, a four-class model was selected as the best fit for the data with similar class counts and distribution of AYA (33.41%, 28.63%, 24.26%, 13.70%). However, the conditional response probabilities of the barrier types differed from those obtained from the imputed dataset, as shown in S2 File.

Sociodemographic and sex-behaviour characteristics of latent classes

The distribution of sexual activity and sociodemographic characteristics by latent classes is shown in S3 Table. As shown in Fig 3, the distribution of AYA across latent classes varied geographically. AYA in the low-risk perception class showed nearly equal distribution between the Northern and Southern zones, ranging from 14.4% to 17.1% in the Northern zones and from 14.5% to 19.5% in the Southern zones. The majority (67.1%) of AYA in the cost and logistics class resided in the Northern zones, ranging from 15.7% (Northcentral) to 28.4% (Northeast). Similarly, 60% of AYA in the testing site class reside in the Northern zones, ranging from 18.5% (Northeast) to 21% (Northwest). Additionally, 60% of AYA in the consent and proximity class reside in the Northern zones, ranging from 18.3% (Northeast) to 21.2% (Northwest).

thumbnail
Fig 3. Spatial map showing zonal geographical distribution of AYA by latent class subgroups.

Map data available from ©OpenStreetMap under the Open Database License.

https://doi.org/10.1371/journal.pone.0300220.g003

Table 4 shows results of the LCR with sociodemographic factors and sexual activity, using the low-risk perception class as the reference category due to its status as the class with the highest proportion of AYA. Multicollinearity diagnostics revealed high positive correlation (0.917) between intergenerational sex and condom use at last sex with non-marital, non-cohabitating partners in the past 12 months. However, VIFs for both variables (6.34 and 7.45, respectively) were below the commonly accepted threshold of 10, indicating that multicollinearity was not severe enough to warrant variable removal [46]. Therefore, both variables were retained in the regression models. Correlation matrix and VIFs are presented in S2File.

thumbnail
Table 4. Sociodemographic and sexual lifestyle correlates of latent classes.

The reference category for odds ratio (OR) is the Low-risk perception class. Bolded values indicate statistical significance as determined by 95% CIs not overlapping 1.00.

https://doi.org/10.1371/journal.pone.0300220.t004

Compared to AYA in the low-risk perception class, AYA in the consent and proximity class were more likely to reside in the Northern regions (aOR 1.80, 95% CI 1.35–2.41 for Northwest; aOR 1.79, 95% CI 1.33–2.42 for Northeast; aOR 1.98, 95% CI 1.52–2.56 for North central) and less likely to be married (aOR 0.71, 95% CI 0.56–0.92). They were more likely to engage in intergenerational sex with partners above 18 years (aOR 1.17, 95% CI 1.02–1.35), more likely to have two or more sexual partners (aOR1.75, 95% CI 1.39–2.20), and engaging in transactional sex (aOR1.50, 95% CI 1.23–1.84). They were less likely to use condoms at the last sex with non-marital, non-cohabiting partners (aOR 0.79, 95% CI 0.63–0.99).

AYA in the testing site class were more likely to reside in the Northern region (aOR 1.70, 95% CI 1.23–2.35 for Northwest; aOR 1.70, 95% CI 1.20–2.40 for Northeast; aOR 1.80, 95% CI 1.38–2.36 for North central) and have a rural residence (aOR 1.25, 95% CI 1.01–1.53). They were also less likely to be educated up to tertiary level (aOR 0.70, 95% CI 0.52–0.95) or be in the top three wealth quintiles (aOR 0.74, 95% CI 0.57–0.95). They were less likely to be married (aOR 0.76, 95% CI 0.59–0.97), more likely to engage in intergenerational relationships with partners above 18 years (aOR 1.21, 95% CI 1.04–1.39) and more likely to engage in transactional sex (aOR1.53, 95% CI 1.26–1.85).

AYA in the cost and logistic class were more likely to be aged 20–24 years (aOR 1.36, 95% CI 1.02–1.81), have rural residence (aOR 1.58, 95% CI 1.04–2.39), they were less likely to be females (aOR 0.74, 95% CI 0.56–0.97), less likely to have at least primary levels of education (aOR 0.63, 95% CI 0.42–0.94), and less likely to belong to middle or higher wealth quintiles (aOR 0.47, 95% CI 0.31–0.71). They were less likely to use condoms (aOR 0.58, 95% CI 0.34–0.98), know their partners’ HIV status (aOR 0.40, 95% CI 0.25–0.63) and more likely to engage in transactional sex (aOR 2.12, 95% CI 1.58–2.84).

To determine the profile of AYA in the low-risk perception class, we reset the reference category by using each of the three other classes individually as reference categories in our analysis. Figures are shown in S4 Table. Compared to other categories, AYA in the low-risk perception class were more likely to reside in the South, to be females, aged 15–19 years, have urban residence, have an education, and belong to the top three wealth quintiles. They were less likely to engage in intergenerational sex, have two or more sexual partners, or engage in transactional sex. They were more likely to know their partner’s HIV status and to use condoms.

Latent class membership and HIV positivity rate

Fig 4 shows HIV positivity rates for the four classes with the national rates among AYA aged 15–24. [9] LCR with distal outcome showed that AYA in the consent and proximity class had a higher likelihood of testing HIV positive (OR 1.68; 95% CI: 1.04–2.71). However, this association was no longer significant after adjusting for sociodemographic factors and sex behaviour (aOR 1.54, 95% CI 1.01–2.36). Adjusted analysis showed female sex, age group 20–24 years, being married or living with a partner, having ‘other’ types of education, of the Christian religion and residing in Southsouth zone as factors associated with a higher likelihood of testing HIV positive. The results of crude and adjusted analysis are shown in Table 5.

thumbnail
Fig 4. HIV positivity rate in barrier classes.

*Source: NAIIS technical report.

https://doi.org/10.1371/journal.pone.0300220.g004

thumbnail
Table 5. Crude and adjusted association between latent class and HIV positivity rates.

https://doi.org/10.1371/journal.pone.0300220.t005

Adjusted analysis during sensitivity analysis showed significant association between barrier subgroup membership and HIV status, with condom use at last sex with non-marital, non-cohabiting partners in the past 12 months, two or more sexual partners in the past 12 months increasing the likelihood of being HIV infected while being female, knowing partners HIV status, and being aged 19–24 years reducing the likelihood of being HIV infected. See S2 File.

Discussion

To our knowledge, this is the first study to explore patterns of barriers to HIV testing services among AYA in the context of sexual and sociodemographic characteristics and HIV status, using a nationally representative data. Among sexually active AYA in Nigeria who had never undergone HIV testing, we identified four subgroups based on the pattern of barriers reported in accessing HIV testing. The subgroups were termed low-risk perception (n = 7,361; 39.5%), consent and proximity (n = 5,163; 27.74%), testing site (n = 4,996; 26.84%), and cost and logistics (n = 1,092; 5.87%). Although previous research in Nigeria has identified all the twelve individual barriers reported in our study [18, 37, 38], our study makes important advancement by delving deeper into how these barriers group together within specific segments of the AYA population, which might inform more tailored combination interventions aiming to simultaneously address multiple needs. For instance, while distance presents a common obstacle in the "Consent and proximity" and "cost and logistics" categories, their unique combinations with other barriers call for different interventions. In the "Consent and proximity" category, the coexistence of testing permission denial and distance barriers could indicate autonomy as the main problem, as autonomy limitation could reflect mobility restriction and lack of independence in accessing testing services. Conversely, the combination of distance, knowledge, and cost barriers within the "cost and logistics" category points to predominantly access challenges with geographical and economic gaps. These challenges require distinct interventions compared to those needed for AYA in the "Consent and proximity" subgroup. Thus, using LCA to situate each barrier in its specific context enables a more comprehensive understanding that can inform the development of well-tailored and potentially more effective combination interventions [33].

We found that the AYA subgroups had shared and unique sexual behaviour characteristics. While AYA in the "low-risk perception" class exhibited sexual behaviours consistent with their perception of having low likelihood of HIV acquisition, the slightly elevated HIV positivity rates in this group suggest potential underestimation of this risk, consistent with previous studies show high rates of inaccurate risk perception among AYA [19, 33, 4750]. Such inaccuracies represent a significant concern for national HIV prevention efforts, given that significant proportions of AYA in the low-risk perception are distributed across four of six zones.

Our observation of AYA in the consent and proximity class suggests that limitation in autonomy could be a common driver of non-utilisation of HIV testing services and observed sex behaviour [34, 51]. Specifically, intergenerational and transactional sex, and multiple concurrent sexual relationships shown in this group have all been linked with limited autonomy within the family or marital context with relationship power imbalances [16, 52, 53]. The prominence of this subgroup within the Northwest region could be explained by well-documented cultural limitations in the sexual and reproductive health rights (SRHR) for women and young people in northern Nigeria [5456], with often restricted autonomy in healthcare decisions and access [5456]. Studies in Nigeria and elsewhere [5456] have linked limited autonomy with poor reproductive, maternal and child health outcomes. Given the ongoing shift towards biomedical approaches to HIV prevention and treatment, such as pre-exposure prophylaxis (PreP) and treatment as prevention (TasP), our study emphasises the need to integrate autonomy-building interventions into health programs as well as address broader sociocultural barriers that limit autonomy and SRHR of women and young people [54, 5663]. Similarly, increased likelihood of intergenerational sex, and transactional sex among AYA in the "testing site" subgroup suggests that informational gaps in HIV prevention information and intervention, including where and how to access testing services, could be a common driver of non-utilisation of HIV testing services and sexual activity observed in this subgroup. The prominence of this subgroup in the Northwest is consistent with studies [64, 65] in Nigeria that have shown that while newer and convenient HIV testing methods such as home-based and self-testing are being introduced to address access barriers to HIV testing, awareness and acceptance remain low in Northern Nigeria. This suggests the need for comprehensive strategies involving education, awareness campaigns, improved accessibility, and stigma reduction efforts.

The proportion of AYA in the "cost and logistics" subgroup is notably higher in the Northeast region, likely linked to the historically poor socioeconomic development of the region, compounded by prolonged conflicts, which might also explain the observed association of the group with rural residence, belonging to the lowest wealth quintiles, and lower educational attainment [40, 66]. Given the subgroup’s elevated proportion of AYA with HIV positive status, the increased likelihood of condomless sex, transactional sex, and lower likelihood of knowledge of partners’ HIV status emphasises the central role of sociodemographic and structural factors in shaping overall HIV vulnerability, including impacting health behaviour and barriers to access [17, 34, 6770]. Notably, our adjusted analysis showed that sociodemographic factors, rather than barrier types, better explain variation in HIV status. In line with other studies, we found that being female [5], age-group 20–24 years [5, 34], being married or living with a partner elevated the risk of HIV infection [13, 54]. In addition, the elevated likelihood of testing HIV positive in the Southsouth zone is consistent with regional HIV positivity trend and pattern in the country [70].

The combination of HIV positivity rates, sociodemographic factors, and sexual behaviour profiles within the four identified classes offers valuable insights into the potential trajectories of HIV vulnerability that AYA might follow. Understanding these trajectories creates an opportunity for early identification and intervention. Notably, although AYA in the "consent and proximity" and "low-risk perception" classes share similar sociodemographic characteristics, they exhibit markedly different sexual behaviours and HIV infection odds, suggesting that they may represent divergent vulnerability patterns within the same AYA subgroup. Implementing interventions that promote autonomy among young people at an early stage of their development can create a favourable environment for positive transitions from the "consent and proximity" profile to the "low-risk perception" profile [58, 59]. This transition increases the likelihood of adopting the "low-risk perception" profile, characterised by sexual activity that reduces vulnerability to HIV. While we acknowledge that the "low-risk perception" profile also presents unique challenges requiring targeted interventions, this proactive approach can lead to long-term benefits in HIV prevention.

Our study has important strengths. Firstly, we utilised a nationally representative dataset with a well-structured design, increasing our findings’ generalizability. Furthermore, using LCR, we identified AYA subgroups with shared and distinctive patterns of HIV testing barriers, sexual activity, sociodemographic characteristics, and HIV positivity rates. Our approach and findings pave the way for the development of tailored, person-centered, and youth-friendly services that cater to different AYA subgroups’ specific needs and preferences [35].

Our study also comes with limitations that offer opportunities for further research. Firstly, the cross-sectional design of the NAIIS restricts our ability to establish causal relationships [71]. Secondly, using self-reported data in the NAIIS may introduce recall and social desirability biases, potentially biasing our estimates [9]. Additionally, the absence of separate analyses for males and females might mask sex-specific differences in latent class composition and other factors we investigated, especially considering the varying reliability of self-reported data between males and females concerning sexual behaviour [72]. Although we attempted to mitigate this limitation by adjusting for sex and other factors when examining the relationship between latent classes and HIV infection, some potential inaccuracies may persist. Moreover, the use of only vaginal sex as a measure of sexual activity in NAIIS excludes the experiences and activities of sexual minority groups, for example. In addition to this, the binary coding of sex in NAIIS excludes transgender and other gender expansive individuals from our analysis. These are significant communities in the context of the HIV epidemic in Nigeria and other settings [73, 74] and future research should focus on sexual behaviours and the current HIV epidemic in these communities. Also focusing solely on vaginal sex and sexual activity to explain HIV positivity might have led us to overlook the significant contribution of other non-sexual transmission routes, such as injection drug use. This oversight is crucial, especially considering that injection drug use is increasingly becoming a significant driver of the HIV epidemic among young people in Nigeria [70]. Additionally, the recoding of variables like religion may obscure important subgroup identities [9]. Lastly, using Latent Class Analysis (LCA) carries the potential for classification errors when determining the most likely class assignment, despite our efforts to minimise this using the integrated 3-step approach in Mplus [27, 43].

The relative consistency in identifying an optimal four-class LCA model and the similarity in class distribution during sensitivity analysis strengthens the reliability of our findings. However, discrepancies between findings from imputed and non-imputed datasets, particularly in the association between barrier subgroup membership and HIV status, and variations in sociodemographic and sexual factors linked to HIV infection, necessitate careful interpretation. As we did not verify whether missing data were missing at random (MAR) or missing completely at random (MCAR), our application of multiple imputation, considered a best practice for handling missing data, may potentially introduce biases in the imputed data [75]. Thus, our results should be interpreted with caution, taking cognisance of findings from both imputed and non-imputed analyses. Nonetheless, the findings present an opportunity for further research. Exploring alternative data handling methods, including multiple imputation with more sophisticated models, can strengthen the robustness of our findings and deepen our understanding the role of barriers to HIV testing, sexual and sociodemographic factors in shaping vulnerability to HIV in adolescents and young people.

Conclusion

In conclusion, our study identified distinct subgroups of AYA based on patterns of barriers to HIV testing services and assessed the association between these barrier patterns and sexual behaviour, socio-demographics, and HIV status between AYA subgroups. We showed that patterns of barriers to HIV testing are linked with differences in sexual behaviour and sociodemographic profiles among AYA, with the latter driving differences in HIV positivity rates. Findings can improve combination healthcare packages aimed at simultaneously addressing multiple barriers and determinants of vulnerability to HIV among AYA. This is highly pertinent as countries face challenges in striking the right balance of targeted and comprehensive programming for AYA.

Supporting information

S1 File. National algorithm for HIV testing used in NAIIS 2018.

https://doi.org/10.1371/journal.pone.0300220.s001

(TIF)

S2 File. Sensitivity analyses and correlation diagnostics.

https://doi.org/10.1371/journal.pone.0300220.s002

(TIF)

S2 Table. Final class counts and proportions for latent classes based on distributed probabilities.

https://doi.org/10.1371/journal.pone.0300220.s004

(TIF)

S3 Table. Sociodemographic and sex behaviour correlates of latent classes.

https://doi.org/10.1371/journal.pone.0300220.s005

(TIF)

S4 Table. Latent class comparison using alternate reference classes.

https://doi.org/10.1371/journal.pone.0300220.s006

(TIF)

Acknowledgments

We thank the Nigeria Federal Ministry of Health for granting study data access and approval. The authors also thank the adolescents and young adults who consented to using their data for research.

References

  1. 1. Frescura L, Godfrey-Faussett P, Feizzadeh A.A., El-Sadr W, Syarif O, Ghys PD, et al. Achieving the 95 95 95 targets for all: A pathway to ending AIDS. Ambrose Z, editor. PLoS ONE [Internet]. 2022 Aug 4 [cited 2023 Aug 30];17(8):e0272405. Available from: https://dx.plos.org/10.1371/journal.pone.0272405 pmid:35925943
  2. 2. Joint United Nations Programme on HIV/AIDS (UNAIDS). 90-90-90: an ambitious treatment target to help end the AIDS epidemic [Internet]. UNAIDS; 2014. Available from: https://www.unaids.org/sites/default/files/media_asset/90-90-90_en_0.pdf
  3. 3. UNAIDS. Ending the AIDS epidemic for adolescents, with adolescents [Internet]. 2016 p. 32. Available from: https://www.unaids.org/sites/default/files/media_asset/ending-AIDS-epidemic-adolescents_en.pdf
  4. 4. Slogrove AL, Sohn AH. The global epidemiology of adolescents living with HIV: Time for more granular data to improve adolescent health outcomes. Curr Opin HIV AIDS [Internet]. 2018 May [cited 2020 Feb 24];13(3):170–8. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5929160/ pmid:29432227
  5. 5. UNAIDS. Young people and HIV [Internet]. 2021 [cited 2023 Oct 10]. Available from: https://www.unaids.org/sites/default/files/media_asset/young-people-and-hiv_en.pdf
  6. 6. UAIDS. 2025 Targets [Internet]. 2020. Available from: https://www.unaids.org/sites/default/files/2025-AIDS-Targets_en.pdf
  7. 7. Slogrove AL, Mahy M, Armstrong A, Davies MA. Living and dying to be counted: What we know about the epidemiology of the global adolescent HIV epidemic. Journal of the International AIDS Society [Internet]. 2017 [cited 2020 Feb 24];20(S3):21520. Available from: https://onlinelibrary.wiley.com/doi/abs/10.7448/IAS.20.4.21520 pmid:28530036
  8. 8. UNAIDS. IN DANGER: UNAIDS Global AIDS Update 2022 [Internet]. Geneva: Joint United Nations Programme on HIV/AIDS; 2022. Available from: https://www.unaids.org/sites/default/files/media_asset/2022-global-aids-update_en.pdf
  9. 9. Federal Ministry of Health, Nigeria. Nigeria HIV/AIDS Indicator and Impact Survey (NAIIS) 2018: Technical Report. [Internet]. Abuja, Nigeria; 2019 Oct [cited 2022 Oct 9]. Available from: http://ciheb.org/media/SOM/Microsites/CIHEB/documents/NAIIS-Report-2018.pdf
  10. 10. Van Den Steene H, Van West D, Glazemakers I. Towards a definition of multiple and complex needs in children and youth: Delphi study in Flanders and international survey. Scandinavian Journal of Child and Adolescent Psychiatry and Psychology [Internet]. 2019 Jan 1 [cited 2023 Sep 18];7(1):60–7. Available from: https://www.sciendo.com/article/10.21307/sjcapp-2019-009 pmid:33520769
  11. 11. Rosengard A, Laing I, Ridley J. A Literature Review on Multiple and Complex Needs. 2007 Jan 1; Available from: https://www.researchgate.net/profile/Ann-Rosengard/publication/242483070_A_Literature_Review_on_Multiple_and_Complex_Needs/links/00b7d530b6b78216af000000/A-Literature-Review-on-Multiple-and-Complex-Needs.pdf
  12. 12. Kaunda-Khangamwa BN, Kapwata P, Malisita K, Munthali A, Chipeta E, Phiri S, et al. Adolescents living with HIV, complex needs and resilience in Blantyre, Malawi. AIDS Res Ther [Internet]. 2020 Dec [cited 2023 Oct 10];17(1):35. Available from: https://aidsrestherapy.biomedcentral.com/articles/10.1186/s12981-020-00292-1
  13. 13. Hughes A, Hope R, Nwokolo N, Ward B, Jones R, Von Schweitzer M, et al. Meeting complex needs: young people with HIV in London: Young people living with HIV. HIV Med [Internet]. 2013 Mar [cited 2023 Oct 10];14(3):145–52. Available from: https://onlinelibrary.wiley.com/doi/10.1111/j.1468-1293.2012.01049.x
  14. 14. Valente PK, Bauermeister JA, Lin WY, Silva DTD, Hightow-Weidman L, Drab R, et al. Preferences Across Pre-Exposure Prophylaxis Modalities Among Young Men Who Have Sex with Men in the United States: A Latent Class Analysis Study. AIDS Patient Care and STDs [Internet]. 2022 Nov [cited 2023 Feb 20];36(11):431–42. Available from: https://www.liebertpub.com/doi/full/ pmid:36367995
  15. 15. Tanser F, Kim HY, Vandormael A, Iwuji C, Bärnighausen T. Opportunities and Challenges in HIV Treatment as Prevention Research: Results from the ANRS 12249 Cluster-Randomized Trial and Associated Population Cohort. Curr HIV/AIDS Rep [Internet]. 2020 [cited 2023 Apr 8];17(2):97–108. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072051/ pmid:32072468
  16. 16. Conroy AA. The influence of relationship power dynamics on HIV testing in rural Malawi. J Sex Res. 2015;52(3):347–59. pmid:24670263
  17. 17. Conroy AA, Ruark A, Tan JY. Re-conceptualising gender and power relations for sexual and reproductive health: contrasting narratives of tradition, unity, and rights. Culture, Health & Sexuality [Internet]. 2020 Apr 20 [cited 2023 Apr 9];22(sup1):48–64. Available from: https://www.tandfonline.com/doi/full/10.1080/13691058.2019.1666428 pmid:31633456
  18. 18. Ajayi AI, Awopegba OE, Adeagbo OA, Ushie BA. Low coverage of HIV testing among adolescents and young adults in Nigeria: Implication for achieving the UNAIDS first 95. PLOS ONE [Internet]. 2020 May 19 [cited 2023 Mar 29];15(5):e0233368. Available from: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0233368 pmid:32428005
  19. 19. Mathur S, Pilgrim N, Patel SK, Okal J, Mwapasa V, Chipeta E, et al. HIV vulnerability among adolescent girls and young women: a multi-country latent class analysis approach. Int J Public Health [Internet]. 2020 May 1 [cited 2023 Feb 20];65(4):399–411. Available from: https://doi.org/10.1007/s00038-020-01350-1 pmid:32270233
  20. 20. Folayan MO, Odetoyinbo M, Brown B, Harrison A. Addressing the Socio-Development Needs of Adolescents Living with HIV/AIDS in Nigeria: A Call for Action.: 9.
  21. 21. Reif LK, Rivera VR, Bertrand R, Belizaire ME, Joseph JMB, Louis B, et al. “FANMI”: A Promising Differentiated Model of HIV Care for Adolescents in Haiti. J Acquir Immune Defic Syndr [Internet]. 2019 Sep 1 [cited 2020 Feb 8];82(1):e11–3. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692183/ pmid:31107305
  22. 22. Reif LK, McNairy ML, Lamb MR, Fayorsey R, Elul B. Youth-friendly services and differentiated models of care are needed to improve outcomes for young people living with HIV. Current Opinion in HIV and AIDS [Internet]. 2018 May [cited 2023 Oct 10];13(3):249–56. Available from: https://journals.lww.com/01222929-201805000-00012 pmid:29432230
  23. 23. Federal Ministry of Health. Nigeria National Standards & Minimum Service Package for Adolescent &Youth-Friendly Health Services [Internet]. 2018. Available from: https://tciurbanhealth.org/wp-content/uploads/2019/02/7-MPSS-Nigeria-National-Standards-vdec-17-FINALE.pdf
  24. 24. Reif LK, Bertrand R, Benedict C, Lamb MR, Rouzier V, Verdier R, et al. Impact of a youth-friendly HIV clinic: 10 years of adolescent outcomes in Port-au-Prince, Haiti. Journal of the International AIDS Society [Internet]. 2016 [cited 2020 Feb 8];19(1):20859. Available from: https://onlinelibrary.wiley.com/doi/abs/10.7448/IAS.19.1.20859 pmid:27389256
  25. 25. Saul J, Bachman G, Allen S, Toiv NF, Cooney C, Beamon T. The DREAMS core package of interventions: A comprehensive approach to preventing HIV among adolescent girls and young women. Bekker LG, editor. PLoS ONE [Internet]. 2018 Dec 7 [cited 2023 Oct 10];13(12):e0208167. Available from: pmid:30532210
  26. 26. Weller BE, Bowen NK, Faubert SJ. Latent Class Analysis: A Guide to Best Practice. Journal of Black Psychology [Internet]. 2020 May [cited 2023 Jun 6];46(4):287–311. Available from: http://journals.sagepub.com/doi/10.1177/0095798420930932
  27. 27. Nylund KL, Asparouhov T, Muthén BO. Deciding on the Number of Classes in Latent Class Analysis and Growth Mixture Modeling: A Monte Carlo Simulation Study. Structural Equation Modeling: A Multidisciplinary Journal [Internet]. 2007 Oct 23;14(4):535–69. Available from: https://doi.org/10.1080/10705510701575396
  28. 28. Asparouhov Tihomir, Muthen Bengt. Auxiliary Variables in Mixture Modeling: Using the BCH Method in Mplus to Estimate a Distal Outcome Model and an Arbitrary Secondary Model [Internet]. Mplus We Notes: No. 21; 2021. Available from: https://www.statmodel.com/examples/webnotes/webnote21.pdf
  29. 29. Aflaki K, Vigod S, Ray JG. Part I: A friendly introduction to latent class analysis. Journal of Clinical Epidemiology [Internet]. 2022 Jul [cited 2023 Aug 31];147:168–70. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0895435622001305 pmid:35636591
  30. 30. Sinha P, Calfee CS, Delucchi KL. Practitioner’s Guide to Latent Class Analysis: Methodological Considerations and Common Pitfalls. Crit Care Med [Internet]. 2021 Jan 1 [cited 2023 Apr 21];49(1):e63–79. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746621/ pmid:33165028
  31. 31. Shaunna L., Clark Bengt Muthén. Relating Latent Class Analysis results to variables not included in the analysis. Available from: https://www.statmodel.com/download/relatinglca.pdf
  32. 32. Harel O, Chung H, Miglioretti D. Latent class regression: Inference and estimation with two‐stage multiple imputation. Biometrical J [Internet]. 2013 Jul [cited 2023 Nov 22];55(4):541–53. Available from: https://onlinelibrary.wiley.com/doi/10.1002/bimj.201200020 pmid:23712802
  33. 33. Comins CA, Rucinski KB, Baral S, Abebe SA, Mulu A, Schwartz SR. Vulnerability profiles and prevalence of HIV and other sexually transmitted infections among adolescent girls and young women in Ethiopia: A latent class analysis. PLOS ONE [Internet]. 2020 May 14 [cited 2023 Apr 9];15(5):e0232598. Available from: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0232598 pmid:32407394
  34. 34. Gottert A, Pulerwitz J, Heck CJ, Cawood C, Mathur S. Creating HIV risk profiles for men in South Africa: a latent class approach using cross-sectional survey data. Journal of the International AIDS Society [Internet]. 2020 Jun 1 [cited 2020 Jun 26];23(S2):e25518. Available from: https://doi.org/10.1002/jia2.25518 pmid:32589340
  35. 35. Parkes A, Waltenberger M, Mercer C, Johnson A, Wellings K, Mitchell K. Latent class analysis of sexual health markers among men and women participating in a British probability sample survey. BMC Public Health [Internet]. 2020 Jan 9 [cited 2023 Feb 22];20(1):14. Available from: https://doi.org/10.1186/s12889-019-7959-7 pmid:31914970
  36. 36. Ajayi AI, Okeke SR. Protective sexual behaviours among young adults in Nigeria: influence of family support and living with both parents. BMC Public Health [Internet]. 2019 Dec [cited 2023 May 24];19(1):983. Available from: https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-019-7310-3 pmid:31337383
  37. 37. Folayan MO, Adebajo S, Adeyemi A, Ogungbemi KM. Differences in Sexual Practices, Sexual Behavior and HIV Risk Profile between Adolescents and Young Persons in Rural and Urban Nigeria. Zhang M, editor. PLoS ONE [Internet]. 2015 Jul 14 [cited 2023 May 24];10(7):e0129106. Available from: https://dx.plos.org/10.1371/journal.pone.0129106 pmid:26171859
  38. 38. Oguegbu A, Beatty F. Relationship between Sexual Risk Behaviors and HIV Counseling and Testing (HCT) Uptake among Young People in Nigeria. Health [Internet]. 2016 [cited 2023 May 24];08(05):463–71. Available from: http://www.scirp.org/journal/doi.aspx?DOI=10.4236/health.2016.85049
  39. 39. Mancini Luca. Comparative Trends in Ethno-Regional Inequalities in Ghana and Nigeria: Evidence from Demographic and Health Surveys. In: Centre for Research on Inequality, Human Security and Ethnicity [Internet]. 2009. Available from: https://assets.publishing.service.gov.uk/media/57a08b69e5274a31e0000b30/workingpaper72.pdf
  40. 40. Okoli CI, Hajizadeh M, Rahman MM, Khanam R. Geographic and socioeconomic inequalities in the survival of children under-five in Nigeria. Sci Rep [Internet]. 2022 May 19 [cited 2023 May 24];12(1):8389. Available from: https://www.nature.com/articles/s41598-022-12621-7 pmid:35590092
  41. 41. Adebowale AS, Yusuf BO, Fagbamigbe AF. Survival probability and predictors for woman experience childhood death in Nigeria: “analysis of north–south differentials.” BMC Public Health [Internet]. 2012 Dec [cited 2023 May 24];12(1):430. Available from: http://bmcpublichealth.biomedcentral.com/articles/10.1186/1471-2458-12-430 pmid:22691616
  42. 42. Latent Class Analysis: A Guide to Best Practice—Bridget E. Weller, Natasha K. Bowen, Sarah J. Faubert, 2020 [Internet]. [cited 2023 Feb 6]. Available from: https://journals.sagepub.com/doi/full/10.1177/0095798420930932
  43. 43. Asparouhov T, Muthén B. Auxiliary Variables in Mixture Modeling: Three-Step Approaches Using Mplus. Structural Equation Modeling: A Multidisciplinary Journal [Internet]. 2014 Jul 3 [cited 2023 Feb 10];21(3):329–41. Available from: https://doi.org/10.1080/10705511.2014.915181
  44. 44. Asparouhov T, Muthen B. Auxiliary Variables in Mixture Modeling: Using the BCH Method in Mplus to Estimate a Distal Outcome Model and an Arbitrary Secondary Model.: 80.
  45. 45. StataCorp. 2021. Stata Statistical Software: Release 17. College Station, TX: StataCorp LLC.
  46. 46. Sohil F, Sohali MU, Shabbir J. An introduction to statistical learning with applications in R: by Gareth James, Daniela Witten, Trevor Hastie, and Robert Tibshirani, New York, Springer Science and Business Media, 2013, $41.98, eISBN: 978-1-4614-7137-7. Statistical Theory and Related Fields [Internet]. 2022 Jan 2 [cited 2024 Jan 21];6(1):87–87. Available from: https://www.tandfonline.com/doi/full/10.1080/24754269.2021.1980261
  47. 47. Clifton S, Nardone A, Field N, Mercer CH, Tanton C, Macdowall W, et al. HIV testing, risk perception, and behaviour in the British population. AIDS [Internet]. 2016 Mar 27 [cited 2023 Apr 9];30(6):943–52. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794135/ pmid:26963528
  48. 48. Dowson L, Kober C, Perry N, Fisher M, Richardson D. Why some MSM present late for HIV testing: a qualitative analysis. AIDS Care. 2012;24(2):204–9. pmid:21780956
  49. 49. Swenson RR, Rizzo CJ, Brown LK, Vanable PA, Carey MP, Valois RF, et al. HIV Knowledge and its Contribution to Sexual Health Behaviors of Low-Income African American Adolescents. J Natl Med Assoc [Internet]. 2010 Dec [cited 2023 Mar 31];102(12):1173–82. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095017/ pmid:21287898
  50. 50. Badru T, Mwaisaka J, Khamofu H, Agbakwuru C, Adedokun O, Pandey SR, et al. HIV comprehensive knowledge and prevalence among young adolescents in Nigeria: evidence from Akwa Ibom AIDS indicator survey, 2017. BMC Public Health [Internet]. 2020 Jan 13;20(1):45. Available from: https://doi.org/10.1186/s12889-019-7890-y pmid:31931760
  51. 51. Badejo O, Nöstlinger C, Wouters E, Laga M, Okonkwo P, Jwanle P, et al. Understanding why and how youth-friendly health services improve viral load suppression among adolescents and young people living with HIV in Nigeria: realist evaluation with qualitative comparative analysis. BMJ Glob Health [Internet]. 2023 Sep [cited 2023 Oct 30];8(9):e012600. Available from: https://gh.bmj.com/lookup/doi/10.1136/bmjgh-2023-012600 pmid:37748794
  52. 52. Wamoyi J, Renju J, Moshabela M, McLean E, Nyato D, Mbata D, et al. Understanding the relationship between couple dynamics and engagement with HIV care services: insights from a qualitative study in Eastern and Southern Africa. Sex Transm Infect [Internet]. 2017 Jul 1 [cited 2023 Mar 12];93(Suppl 3). Available from: https://sti.bmj.com/content/93/Suppl_3/e052976 pmid:28736395
  53. 53. Dovel K, Dworkin SL, Cornell M, Coates TJ, Yeatman S. Gendered health institutions: examining the organization of health services and men’s use of HIV testing in Malawi. Journal of the International AIDS Society [Internet]. 2020 Jun 1 [cited 2020 Jun 26];23(S2):e25517. Available from: https://doi.org/10.1002/jia2.25517 pmid:32589346
  54. 54. Stoner MCD, Haley DF, Golin CE, Adimora AA, Pettifor A. The relationship between economic deprivation, housing instability and transactional sex among women in North Carolina (HPTN 064). AIDS Behav [Internet]. 2019 Nov [cited 2023 Apr 9];23(11):2946–55. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374930/ pmid:31332597
  55. 55. Kilburn K, Ranganathan M, Stoner MCD, Hughes JP, MacPhail C, Agyei Y, et al. Transactional sex and incident HIV infection in a cohort of young women from rural South Africa. AIDS [Internet]. 2018 Jul 31 [cited 2023 Apr 9];32(12):1669. Available from: https://journals.lww.com/aidsonline/fulltext/2018/07310/transactional_sex_and_incident_hiv_infection_in_a.13.aspx pmid:29762176
  56. 56. UNAIDS. Transactional sex and HIV risk: from analysis to action. Joint United Nations Programme on HIV/AIDS [Internet]. 2018; Available from: https://www.unaids.org/sites/default/files/media_asset/transactional-sex-and-hiv-risk_en.pdf
  57. 57. Rwafa T, Shamu S, Christofides N. Relationship power and HIV sero-status: an analysis of their relationship among low-income urban Zimbabwean postpartum women. BMC Public Health [Internet]. 2019 Jun 21 [cited 2023 Mar 12];19(1):792. Available from: https://doi.org/10.1186/s12889-019-7137-y pmid:31226980
  58. 58. Gu LY, Zhang N, Mayer KH, McMahon JM, Nam S, Conserve DF, et al. Autonomy-Supportive Healthcare Climate and HIV-Related Stigma Predict Linkage to HIV Care in Men Who Have Sex With Men in Ghana, West Africa. J Int Assoc Provid AIDS Care [Internet]. 2021 Jan 1 [cited 2023 Mar 12];20:2325958220978113. Available from: pmid:33733909
  59. 59. Vijayaraghavan J, Vidyarthi A, Livesey A, Gittings L, Levy M, Timilsina A, et al. Strengthening adolescent agency for optimal health outcomes. BMJ [Internet]. 2022 Oct 27 [cited 2022 Nov 19];e069484. Available from: https://www.bmj.com/lookup/doi/10.1136/bmj-2021-069484 pmid:36302546
  60. 60. James-Hawkins L, Peters C, VanderEnde K, Bardin L, Yount KM. Women’s agency and its relationship to current contraceptive use in lower- and middle-income countries: A systematic review of the literature. Global Public Health [Internet]. 2018 Jul 3 [cited 2022 Nov 19];13(7):843–58. Available from: https://www.tandfonline.com/doi/full/10.1080/17441692.2016.1239270 pmid:27690750
  61. 61. Catalano RF, Skinner ML, Alvarado G, Kapungu C, Reavley N, Patton GC, et al. Positive Youth Development Programs in Low- and Middle-Income Countries: A Conceptual Framework and Systematic Review of Efficacy. Journal of Adolescent Health [Internet]. 2019 Jul [cited 2022 Nov 19];65(1):15–31. Available from: https://linkinghub.elsevier.com/retrieve/pii/S1054139X19300667 pmid:31010725
  62. 62. Alvarado G., Skinner M., Plaut D., AlvMoss C., Kapungu C., Reavley N. A Systematic Review of Positive Youth Development Programs in Low- and Middle-Income Countries. 2017; Available from: https://pdf.usaid.gov/pdf_docs/PA00MR58.pdf
  63. 63. Iliyasu Z, Galadanci HS, Musa AH, Iliyasu BZ, Nass NS, Garba RM, et al. HIV self‐testing and repeat testing in pregnancy and postpartum in Northern Nigeria. Tropical Med Int Health [Internet]. 2022 Jan [cited 2023 Oct 15];27(1):110–9. Available from: https://onlinelibrary.wiley.com/doi/ pmid:34981875
  64. 64. Iliyasu Z, Kassim RB, Iliyasu BZ, Amole TG, Nass NS, Marryshow SE, et al. Acceptability and correlates of HIV self-testing among university students in northern Nigeria. Int J STD AIDS [Internet]. 2020 Aug [cited 2023 Oct 15];31(9):820–31. Available from: http://journals.sagepub.com/doi/ pmid:32623978
  65. 65. Omole O, Welye H, Abimbola S. Boko Haram insurgency: implications for public health. The Lancet [Internet]. 2015 Mar [cited 2023 Oct 15];385(9972):941. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0140673615602070 pmid:25747581
  66. 66. Jooste S, Mabaso M, Taylor M, North A, Shean Y, Simbayi LC. Socio-economic differences in the uptake of HIV testing and associated factors in South Africa. BMC Public Health [Internet]. 2021 Aug 26 [cited 2023 Apr 9];21(1):1591. Available from: pmid:34445996
  67. 67. Njau B, Mhando G, Jeremiah D, Mushi D. Correlates of Sexual Risky Behaviours, HIV Testing, and HIV Testing Intention among Sexually Active Youths in Northern Tanzania. East Afr Health Res J [Internet]. 2021 [cited 2023 Apr 9];5(2):151–8. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751422/ pmid:35036841
  68. 68. Xu H, Xie J, Xiao Z, Xiao H, Li X, Goldsamt L, et al. Sexual attitudes, sexual behaviors, and use of HIV prevention services among male undergraduate students in Hunan, China: a cross-sectional survey. BMC Public Health [Internet]. 2019 Feb 28 [cited 2023 Apr 9];19:250. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396457/ pmid:30819255
  69. 69. Piot P, Greener R, Russell S. Squaring the Circle: AIDS, Poverty, and Human Development. PLoS Med [Internet]. 2007 Oct [cited 2023 Apr 9];4(10):e314. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2039763/
  70. 70. Onovo AA, Adeyemi A, Onime D, Kalnoky M, Kagniniwa B, Dessie M, et al. Estimation of HIV prevalence and burden in Nigeria: a Bayesian predictive modelling study. eClinicalMedicine [Internet]. 2023 Aug [cited 2023 Oct 15];62:102098. Available from: https://linkinghub.elsevier.com/retrieve/pii/S2589537023002754 pmid:37538543
  71. 71. Creswell JW, Plano Clark VL. Designing and conducting mixed methods research. Thousand Oaks, Calif: SAGE Publications; 2007. 275 p.
  72. 72. Lindgren KP, Parkhill MR, George WH, Hendershot CS. Gender Differences in Perceptions of Sexual Intent: A Qualitative Review and Integration. Psychology of Women Quarterly [Internet]. 2008 Dec [cited 2023 Oct 14];32(4):423–39. Available from: http://journals.sagepub.com/doi/10.1111/j.1471-6402.2008.00456.x pmid:19763282
  73. 73. Eluwa GIE, Adebajo SB, Eluwa T, Ogbanufe O, Ilesanmi O, Nzelu C. Rising HIV prevalence among men who have sex with men in Nigeria: a trend analysis. BMC Public Health [Internet]. 2019 Dec [cited 2023 Oct 15];19(1):1201. Available from: https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-019-7540-4 pmid:31477073
  74. 74. Sandfort TGM, Mbilizi Y, Sanders EJ, Guo X, Cummings V, Hamilton EL, et al. HIV incidence in a multinational cohort of men and transgender women who have sex with men in sub-Saharan Africa: Findings from HPTN 075. Blackard JT, editor. PLoS ONE [Internet]. 2021 Feb 25 [cited 2023 Oct 15];16(2):e0247195. Available from: pmid:33630925
  75. 75. Sterne JAC, White IR, Carlin JB, Spratt M, Royston P, Kenward MG, et al. Multiple imputation for missing data in epidemiological and clinical research: potential and pitfalls. BMJ [Internet]. 2009 Jun 29 [cited 2020 Mar 22];338. Available from: https://www.bmj.com/content/338/bmj.b2393 pmid:19564179