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

Noncommunicable diseases risk factors and the risk of COVID-19 among university employees in Indonesia

  • Indah Suci Widyahening ,

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

    indah_widyahening@ui.ac.id

    Affiliations Department of Community Medicine, Faculty of Medicine, Universitas Indonesia, Jakarta Pusat, Indonesia, Southeast Asian Ministers of Education Organization—Regional Centre for Food and Nutrition (SEAMEO-RECFON)—Pusat Kajian Gizi Regional (PKGR), Universitas Indonesia, Jakarta, Indonesia

  • Dhanasari Vidiawati,

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

    Affiliation Department of Community Medicine, Faculty of Medicine, Universitas Indonesia, Jakarta Pusat, Indonesia

  • Trevino A. Pakasi,

    Roles Data curation, Funding acquisition, Investigation, Methodology, Writing – review & editing

    Affiliation Department of Community Medicine, Faculty of Medicine, Universitas Indonesia, Jakarta Pusat, Indonesia

  • Pradana Soewondo,

    Roles Conceptualization, Funding acquisition, Writing – review & editing

    Affiliation Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia–Cipto Mangunkusumo Hospital, Jakarta Pusat, Indonesia

  • Abdillah Ahsan

    Roles Formal analysis, Investigation, Writing – review & editing

    Affiliation Department of Economics, Faculty of Economics and Business, Universitas Indonesia, Depok, Indonesia

Abstract

Introduction

Noncommunicable diseases (NCDs) are still a major public health problem in Indonesia. Studies have shown that risk factors of NCDs are associated with coronavirus disease 2019 (COVID-19) severity and mortality. However, it is unclear whether NCD risk factors are also risks for new COVID-19 cases. This study aimed to obtain an NCD risk profile among university employees and its associations with contracting COVID-19.

Methods

A cross-sectional study was conducted in October 2021. Participants were administrative employees of Universitas Indonesia (UI), Depok City, West Java. Assessment of NCD risk factors was based on the World Health Organization STEPwise approach to NCD risk factor surveillance (WHO STEPS). Demographic, working, and medical-history data were obtained electronically by using a Google Form. Physical and laboratory examinations were done in the Integrated Post for NCDs. Risks were expressed as adjusted odds ratio (ORadj) and 95% confidence interval (CI) in multivariate analyses.

Results

A total of 613 employees were enrolled. Men were predominant (54.8%), and about 36% of them work in shift as security personnel. About 66.7% were overweight or obese and 77.8% had hypertension. There were 138 (22.8%) employees who had COVID-19. Nearly all (95.6%) had been fully vaccinated against COVID-19. At-risk waist circumference (ORadj 1.72, 95% CI 1.15–2.56, p = 0.008) and total cholesterol level of 200–239 mg/dL (ORadj 2.30, 95% CI 1.19–4.44, p = 0.013) were independent risk factors, but shift work (ORadj 0.52, 95% CI 0.34–0.80, p = 0.003) was protective against COVID-19.

Conclusion

The prevalence of NCD risk factors among university administrative employees was high, increasing the risk of contracting COVID-19. A behavioral intervention program to manage NCD risk factors at the university level is urgently needed according to the Health Promoting University framework.

Introduction

The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is ongoing and has possibly become endemic. Currently, community transmission of COVID-19 in Indonesia has remained at a low level after a second dramatic peak in mid-July 2021 [1]. However, the actual number of cases may be higher than officially registered; the weighted estimate of seroprevalence of the SARS-CoV-2 antibody in Jakarta in March 2021 was 44.5%. This implies that almost half of the population has been infected with SARS-CoV-2 [2].

Noncommunicable diseases (NCDs) are major health problems in the world. The national Basic Health Research in 2018 has shown increasing prevalence of NCDs in Indonesia, such as diabetes (from 6.9% in 2013 to 10.9% in 2018) and hypertension (from 25.8% in 2013 to 34.1% in 2018) [3]. Early in the COVID-19 pandemic, patients needing intensive care were more likely to have NCDs as comorbidities (hypertension, diabetes, cardiovascular disease, and cerebrovascular disease) [4].

The association between NCD risk factors and COVID-19 is not clear. Previous data showed that body mass index (BMI) and obesity are associated with SARS-CoV-2 infection, hospitalization, and mortality [5, 6]. Obesity seems to play an important role in the pathogenesis of COVID-19 [7]. Multimorbidity, especially renal, cardiovascular, and metabolic morbidities, is associated with a higher risk of a COVID-19 positive test [8, 9].

To prevent new infections, we need to identify modifiable risk factors against contracting COVID-19, such as obesity and/or components of metabolic syndrome. This is important because factors that can be modified to reduce risk will be the target for health education along with a rigorous vaccination program. This study aimed to obtain the NCD risk profiles among university employees and its association with contracting COVID-19.

Methods

Study design and participants

The design of this study was cross-sectional and conducted in October 2021. Participants were employees of the University Central Administration, Universitas Indonesia (UI) and the administrative/supporting staffs of the Faculty Medicine of the university. Demographic, working, and medical-history data were obtained electronically by using a Google Form, which was distributed through the WhatsApp group of the Directorate of Human Resources and the Faculty of Medicine. Participants were then invited to attend physical and laboratory examination in the Integrated Post for NCDs throughout Universitas Indonesia at the main campus in Depok City, West Java and the Salemba campus in Jakarta (total six posts). This post was a community-based program oriented toward promotive and preventive efforts to control NCDs [10].

Sample size was calculated using the formula for a prevalence study with a confidence level of 0.05 and precision of 5%. Hence, a minimum number of 384 subjects was expected. Participants were enrolled in this study if they provided written consent. Ethics approval was granted from the Health Research Ethic Committee of the Faculty of Medicine Universitas Indonesia–Cipto Mangunkusumo Hospital (No. KET-1006/UN2.F1/ETIK/PPM.00.02/2021). Written informed consent was requested from all participants prior to the study.

History of COVID-19 and vaccination

A diagnosis of COVID-19 was established as a history of a positive PCR or rapid-detection test for SARS-CoV-2 from nasopharyngeal swabs. However, since this type of question could be seen as a sensitive question to some of the participants, we offered a “prefer not to answer” option as an answer choice. A history of COVID-19 was counted once between March 2020 and October 2021; re-infection, if it had occurred, was not considered. Participants were also asked whether or not they were hospitalized as a result of having COVID-19.

The COVID-19 vaccination campaign began in January 2021 (in the UI Hospital), and by mid-2021, most non-medical university employees had been scheduled for two doses.

Assessment of noncommunicable diseases risk factors

Assessment was based on the World Health Organization STEPwise approach to NCD risk factor surveillance (STEPS) [11]. The survey instrument includes: tobacco use, alcohol use, physical inactivity, unhealthy diet, and key biological risk factors: overweightness and obesity, raised blood pressure, raised blood glucose, and abnormal blood lipids. Risk factors assessed in this study consisted of anthropometric measurements (BMI and waist circumference), medical history (hypertension, diabetes, dyslipidemia), working pattern (shift or non-shift), behavioral risk factors (smoking; alcohol consumption; fruit, vegetable, and salt consumption; level of physical activity), and blood chemistry results (fasting blood glucose; triglyceride; and total, low-density lipoprotein (LDL), and high-density lipoprotein (HDL) cholesterol levels).

Body weight was measured using a weight scale (SECA, Hamburg, Germany), and body height was measured using a stature meter microtoise (GEA medical). BMI was calculated as body weight in kilograms divided by body height in meters squared. Nutritional status was then classified based on the BMI criteria for an Asian population as follows: underweight (BMI <18.5 kg/m2), normal weight (18.5–22.9 kg/m2), overweight (23.0–24.9 kg/m2), obesity class I (25.0–29.9 kg/m2), and obesity class II (>30.0 kg/m2) [12]. Waist circumference (WC) was measured using a measuring tape (Onemed Waist Ruler OD 235). At-risk WC was >102 cm for men and >88 cm for women.

Systolic and diastolic blood pressures (BP) were measured using a digital blood pressure monitor (Beurer® BM 58, Germany). Similar measurement tools were used for all participants. Hypertension Elevated blood pressure was indicated if systolic BP was ≥130 mmHg and/or diastolic BP ≥85 mmHg. A minimum of 8 h fasting was required for the measurement of fasting blood glucose (FBG), triglyceride (TG), and cholesterol levels. The result was indicated as high if FBG ≥110 mg/dL, TG ≥ 150 mg/dL, total cholesterol ≥200 mg/dL, and LDL-cholesterol ≥100 mg/dL; while HDL-cholesterol was considered low if ≤40 mg/dL, based on the metabolic syndrome criteria by the American Heart Association/National Heart, Lung, and Blood Institute [13]. Physical activity was considered low (inactive) if less than 150 min of moderate-intensity physical activity or less than 75 min of vigorous-intensity physical activity per week was reported [14].

Statistical analyses

Baseline characteristics of the participants and risk factors were presented descriptively. Univariate logistic regression test was performed for each risk factor. Multivariate logistic regression analyses were done to estimate the adjusted odds ratio (ORadj) and its corresponding 95% confidence intervals (CIs) for the association between risk factor and SARS-CoV-2 infection. Adjustments were made to all other variables included in the multivariate logistic regression (variables that had a p value of <0.2 in the univariate analysis). Missing data were excluded from the analysis including the “prefer not to answer” response. All statistical analyses were done using Statistical Package for Social Science (SPSS) version 20. A p value of less than 0.05 was considered significant.

Results

Characteristics of the study subjects

From 789 supporting staff members invited, 750 attended the examination, 618 completed the questionnaires, and 5 did not undergo laboratory tests. In total, 613 (77.7%) participants were included in the final analyses. However, there were missing data in several variables (less than 2% participants for each variable). Table 1 shows the characteristics and health history of the university employees. Male participants were predominant (54.8%). Around 76.7% of them were 40 years old or younger, and 72.4% were married. About 36% (222 of 613) work in shifts as security personnel. There were 138 (22.8%) employees who had had COVID-19, but only 14 (2.3%) had required hospitalization. Nearly all the participants (94.0%) were fully vaccinated against COVID-19.

thumbnail
Table 1. Characteristics and health history of the university employees (n = 613).

https://doi.org/10.1371/journal.pone.0263146.t001

Table 2 shows the distribution of behavioral risk factors for NCDs among the university employees. The proportion of those who currently smoke is nearly 25% (151 of 613) and 15.2% (93 of 613) admitted consuming alcohol. The proportion of those who consume fruit 5–7 days per week was just below 20% (119 of 613), while the percentage of those who consume vegetables was also low (below 50%) (282 of 613). The majority of the respondents (94.3%) were categorized as having an active physical activity level.

thumbnail
Table 2. Behavioral risk factors for non-communicable diseases among university employees (n = 613).

https://doi.org/10.1371/journal.pone.0263146.t002

Table 3 shows biological risk factors for NCDs among the university employees. Two-thirds of them (409 of 613) were categorized as overweight and obese, more than 75% (477 of 613) had increased blood pressure, half (320 of 613) had an at at-risk waist circumference, and almost half (294 of 613) had increased fasting blood sugar levels.

thumbnail
Table 3. Biological risk factors for noncommunicable diseases among university employees (n = 613).

https://doi.org/10.1371/journal.pone.0263146.t003

Univariate analyses between each risk factors with SARS-CoV-2 infection are presented in the (S1S3 Tables). Table 4 shows the risk factors associated with SARS-CoV-2 infection based on multivariate logistic regression. The final model of multivariate logistic regression revealed that shift work (adjusted OR [ORadj] 0.52, 95% confidence interval [CI] 0.34–0.80, p = 0.003), having an at-risk waist circumference (ORadj 1.72, 95% CI 1.15–2.56, p = 0.008), and a total cholesterol level of 200–239 mg/dl (ORadj 2.30, 95% CI 1.19–4.44, p = 0.013) are variables that have a significant relationship with a history of COVID-19.

thumbnail
Table 4. Risk factors associated with COVID-19 among university employees (n = 605).

https://doi.org/10.1371/journal.pone.0263146.t004

Discussion

Our study showed that more than half of the university employees have at least one biological risk factor associated with NCDs (overweight or obese, increased blood pressure, at-risk waist circumference, and increased fasting blood sugar). Having an at-risk waist circumference and a total cholesterol level of 200–239 mg/dL increased the risk of contracting COVID-19 while working in shift prevented it.

Assessing the NCD risk factors was our university’s commitment to protecting health and promoting the well-being of our university members as part of the Health Promoting University framework [15]. It seems that NCD risk factors are common among university employees. A study in Saudi Arabia also found that more than half of university employees there had three or more NCD risk factors, i.e., 64% were overweight or obese, 22.1% had hypertension, and 21.5% had diabetes [16]. Another study showed that 72% of the university employees and their families were overweight or obese [17]. In Nigeria, the most common risk factors among university employees were inadequate intake of fruit and vegetables (94.6%), physical inactivity (77.8%), and dyslipidemia (51.8%) [18].

Early in the COVID-19 pandemic, obesity was identified as a significant risk factor for severe disease [19, 20]. A population-based cohort study found that excess weight is an important modifiable risk factor for severe COVID-19 outcomes [21]. Meta-analyses confirmed that obesity is a risk factor for developing severe COVID-19 through several possible mechanisms [22]. Obesity is considered a low-grade, persistent inflammation. Pro-inflammatory cytokines are elevated in obesity due to dysregulation of normal adipose homeostasis. Hypertrophic adipocytes lead to insulin resistance and inflammation [23]. These changes might ultimately result in impairment of host immune defense that had been associated with increased susceptibility to severe disease and poor outcomes in obese COVID-19 patients [24]. Little is known about obesity as a risk factor for contracting COVID-19. A recent review suggested that obesity increases susceptibility to SARS-CoV-2 infection due to changes in immune pathophysiology, including the increased production of pro-inflammatory cytokines, adipokines, and leptin [25].

A recent study found that the ratio of adiponectin to leptin (Adpn/Lep) was positively correlated with C-reactive protein level, a marker of systemic inflammation. Increased production of Adpn/Lep was caused by increased adiponectin and reduced leptin; it might be a compensatory response to systemic inflammation [26]. Leptin is an adipocytokine that is involved in various physiological functions, and it maintains homeostasis in the immune system [27]. Obesity, increased leptin, and leptin resistance are associated with severe COVID-19. Leptin is the link between metabolic and immunity responses involving T-cell activation upon an acute respiratory viral infection, including SARS-CoV-2. In obesity, there is a large dysregulation of endocrine and inflammatory events leading to an inadequate immune response to acute SARS-CoV-2 infection [28, 29].

A large cohort study from the general population in the UK found that modifiable risk factors for contracting COVID-19 were a higher BMI, higher glycated hemoglobin, smoking, a slow walking pace (a proxy for physical fitness), and the use of blood pressure medication (a proxy for hypertension). A high level of HDL cholesterol was associated with lower risk. The authors concluded that lifestyle modification might reduce the risk of contracting COVID-19 [30]. Another study found that higher total cholesterol and ApoB levels might increase the risk of SARS-CoV-2 infection [31].

Many studies use BMI as an indicator of obesity, which delineates excessive body fat. However, a higher BMI may not represent a higher amount of body fat since it cannot distinguish between fat and lean body mass [32]. We found that high BMI did not have a significant association with the incidence of COVID-19 but high waist circumference (WC) did; the significance was not lost after adjustment for BMI.

Clinical studies on abdominal obesity and COVID-19 are still evolving. One study found that abdominal obesity was associated with a high chest x-ray severity score better than BMI [33]. A UK study found that high WC was associated with a positive test for the SARS-CoV-2 virus only in people ≥ 65 years, independent of BMI [34]. Another study found a positive association between WC and COVID-19 susceptibility (OR = 1.38; 95% CI: 1.07–1.78; p = 0.015). However, the significance was lost after adjustment for BMI. The authors concluded that overall obesity has a causal impact on the susceptibility to COVID-19 and obese people are regarded as high-risk [35].

The ACE2 receptor plays an important role in SARS-COV-2 infectivity as the virus uses the receptor to attach itself to the cell surface [36]. ACE2 is widely expressed in fat and may be the reason why obese patients experience more severe COVID-19 symptoms [37]. A recent study found that the expression of ACE2 in fat tissue (both visceral and subcutaneous) is higher than in lung tissue [38]. Upon binding to the cell surface, SARS-CoV-2 may enter the cell through clathrin-mediated endocytosis of the cell membrane [39]. Human cell membrane contains cholesterol, a key structural lipid that is often used by pathogens for their pathogenesis [40]. Therefore, higher membrane cholesterol provides higher efficiency in viral entry. However, COVID-19 patients have generally shown reduced total cholesterol, HDL, and LDL-cholesterol levels which are associated with disease severity [41]. A systematic review confirmed that lower total, HDL- and LDL-cholesterol levels were significantly associated with COVID-19 severity and mortality but not triglyceride level [42].

In our study, working in shift was a protective factor against contracting COVID-19. These were the security guards who work individually and mostly outdoor, thereby reducing the risk of COVID-19 transmission. On the contrary, a study in the UK found that shift work was associated with increased risk of contracting COVID-19 [43]. More detailed analyses showed that shift work was associated with a higher likelihood of contracting COVID-19 for both irregular (OR 2.42; 95% CI 1.92–3.05) and permanent shift work (OR 2.50; 95% CI 1.95–3.19) [44]. However, unlike our study, the UK cohort enrolled people with various occupations.

There were several limitations in this study. Firstly, the design was not prospective and included only people who survived COVID-19. Therefore, this study potentially suffered from selection and recall biases. Information on the history of risk factors might have also suffered from recall bias, but in the analyses, we used objective data from the current physical examination and laboratory test results. Secondly, we cannot differentiate between whether the participants had COVID-19 before or after vaccination, and most of the employees completed their vaccination schedule about three months before our data collection. Therefore, the effect of the COVID-19 vaccine on the incidence was not known. Universitas Indonesia is one of the most prominent universities in Indonesia, located in an area where the prevalence of NCDs and COVID-19 is the highest in the country. Hence, the prevalence of COVID-19 and NCD risk factors reported in this study might also be higher than other university employees in Indonesia.

Conclusion

University administrative employees have a substantially high prevalence of NCD risk factors, and this has increased their risk of contracting COVID-19. A behavioral intervention program to manage the NCD risk factors at the university level is urgently needed according to the Health Promoting University framework.

Supporting information

S1 Table. Univariate analysis between characteristics and health history of the university employees with COVID-19 (n = 605).

https://doi.org/10.1371/journal.pone.0263146.s001

(DOCX)

S2 Table. Univariate analysis between behavioral risk factors for non-communicable diseases and COVID-19 among university employees (n = 605).

https://doi.org/10.1371/journal.pone.0263146.s002

(DOCX)

S3 Table. Univariate analysis between biological risk factors for noncommunicable diseases and COVID-19 among university employees (n = 605).

https://doi.org/10.1371/journal.pone.0263146.s003

(DOCX)

Acknowledgments

The authors would like to express their gratitude to the Director of Human Resources of Universitas Indonesia and the Dean Office of the Faculty of Medicine Universitas Indonesia for their support during data collection. The authors also thank the Makara Satellite Clinic of Universitas Indonesia for their assistance in the physical and laboratory examination of the subjects. Likewise, the authors are thankful for the assistance of Firky Ditha Saputri, MD and Helisa Rachel, MD during data collection and analysis.

References

  1. 1. World Health Organization. Indonesia Situation Report– 81. Available at: https://cdn.who.int/media/docs/default-source/searo/indonesia/covid19/external-situation-report-81_17-november-2021.pdf?sfvrsn=9edbe641_5.
  2. 2. Ariawan I, Jusril H, Farid MN, Riono P, Wahyuningsih W, Widyastuti, et al. SARS-CoV-2 antibody seroprevalence in Jakarta, Indonesia: March 2021. Available at SSRN: https://ssrn.com/abstract=3954041.
  3. 3. Ministry of Health (MoH), Republic of Indonesia. National Institute of Health Research and Development. Basic Health Research 2018. Jakarta: MoH, 2018.
  4. 4. Wang D, Hu B, Hu C, Zhu F, Liu X, Zhang J, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel Coronavirus-infected pneumonia in Wuhan, China. JAMA. 2020;323:1061–9. pmid:32031570
  5. 5. Tartof SY, Qian L, Hong V, Wei R, Nadjafi RF, Fischer H, et al. Obesity and mortality among patients diagnosed with COVID-19: results from an integrated health care organization. Ann Intern Med. 2020;173(10):773–81. pmid:32783686
  6. 6. Hendren NS, de Lemos JA, Ayers C, Das SR, Rao A, Carter S, et al. Association of body mass index and age with morbidity and mortality in patients hospitalized with COVID-19: Results from the American Heart Association COVID-19 Cardiovascular Disease Registry. Circulation. 2021; 143(2):135–44. pmid:33200947
  7. 7. Kassir R. Risk of COVID-19 for patients with obesity. Obes Rev. 2020;21(6):e13034. pmid:32281287
  8. 8. McQueenie R, Foster HME, Jani BD, et al. Multimorbidity, polypharmacy, and COVID-19 infection within the UK Biobank cohort. PLoS One 2020;15:e0238091. pmid:32817712
  9. 9. Woolford SJ, D’Angelo S, Curtis EM, Parsons CM, Ward KA, Dennison EM, et al. COVID-19 and associations with frailty and multimorbidity: a prospective analysis of UK Biobank participants. Aging Clin Exp Res 2020;32:1897–1905. pmid:32705587
  10. 10. Tri Siswati T, Margono , Husmarini N, Purnamaningrum YE, Bunga Astria Paramashanti BA. Health-promoting university: the implementation of an integrated guidance post for non-communicable diseases (Posbindu PTM) among university employees. Global Health Promotion. 2021 (accepted article). pmid:34269118
  11. 11. World Health Organization. STEPwise Approach to NCD Risk Factor Surveillance (STEPS). Available at: https://www.who.int/teams/noncommunicable-diseases/surveillance/systems-tools/steps.
  12. 12. World Health Organization. Regional Office for the Western Pacific. The Asia-Pacific perspective: redefining obesity and its treatment. Sydney, Australia: Health Communications Australia, 2000.
  13. 13. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, et al. Diagnosis and Management of the Metabolic Syndrome. An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005;112:2735–52. pmid:16157765
  14. 14. Surveillance and Population-Based Prevention Prevention of Noncommunicable Diseases Department, World Health Organization. Global Physical Activity Questionnaire (GPAQ) Analysis Guide, Geneva. Downloaded from: www.who.int/chp/steps.
  15. 15. Mónica Suárez-Reyes M, Van den Broucke S. Implementing the Health Promoting University approach in culturally different contexts: a systematic review. Global Health Prom. 2016; 23 Supp. 1: 46–56. pmid:27199017
  16. 16. Amin TT, Al Sultan AI, Mostafa OA, Darwish AA, Al-Naboli MR. Profile of Non-Communicable Disease Risk Factors Among Employees at a Saudi University. Asian Pac J Cancer Prev. 2014;15 (18):7897–7. pmid:25292084
  17. 17. Alzeidan R, Rabiee F, Mandil A, Hersi A, Fayed A. Non-communicable disease risk factors among employees and their families of a Saudi university: An epidemiological study. PLoS ONE. 2016;11(11): e0165036. pmid:27814369
  18. 18. Agaba EI, Akanbi MO, Agaba PA, Ocheke AN, Gimba ZM, Daniyam S, et al. A survey of non-communicable diseases and their risk factors among university employees: a single institutional study. Cardiovasc J Afr 2017; 28: 377–84. pmid:28820539
  19. 19. Földi M, Farkas N, Kiss S, et al. Obesity is a risk factor for developing critical condition in COVID-19 patients: a systematic review and meta-analysis. Obes Rev 2020; 21: e13095. pmid:32686331
  20. 20. Huang Y, Lu Y, Huang Y-M, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism 2020; 113: 154378. pmid:33002478
  21. 21. Gao M, Piernas C, Astbury NM, Hippisley-Cox J, O’Rahilly S, Aveyard P, et al. Associations between body-mass index and COVID-19 severity in 6.9 million people in England: a prospective, community-based, cohort study. Lancet Diabetes Endocrinol 2021; 9: 350–9. pmid:33932335
  22. 22. Aghili SMM, Ebrahimpur M, Arjmand B, Shadman Z, Pejman Sani M, Qorbani M, et al. Obesity in COVID-19 era, implications for mechanisms, comorbidities, and prognosis: a review and meta-analysis. Int J Obes (Lond). 2021;45(5):998–1016. https://doi.org/10.1038/s41366-021-00776-8.
  23. 23. Kane H, Lynch L. Innate immune control of adipose tissue homeostasis. Trends Immunol. 2019;40:857–72. pmid:31399336
  24. 24. Mohammad S, Aziz R, Al Mahri S, Malik SS, Haji E, Khan AH, et al. Obesity and COVID-19: what makes obese host so vulnerable? Immun Ageing. 2021;18:1. pmid:33390183
  25. 25. Moreno-Fernandez J, Ochoa J, Ojeda ML, Nogales F, Carreras O, Díaz-Castro J. Inflammation and oxidative stress, the links between obesity and COVID-19: a narrative review. J Physiol Biochem. 2022 (in press). pmid:35316507
  26. 26. Di Filippo L, De Lorenzo R, Sciorati C, Capobianco A, Lorè NI, Giustina A, et al. Adiponectin to leptin ratio reflects inflammatory burden and survival in COVID-19. Diab Metab. 2021;47(6):101268. pmid:34333093
  27. 27. de Candia P, Prattichizzo F, Garavelli S, Alviggi C, La Cava A, Matarese G. (2021). The pleiotropic roles of leptin in metabolism, immunity, and cancer. J Exp Med. 2021;218:e20191593. pmid:33857282
  28. 28. Muskiet FAJ, Carrera-Bastos P, Pruimboom L, Lucia A, Furman D. Obesity and leptin resistance in the regulation of the type I interferon early response and the increased risk for severe COVID-19. Nutrients. 2022;14(7):1388. pmid:35406000
  29. 29. Bruno A, Ferrante G, Di Vincenzo S, Pace E, La Grutta S. Leptin in the respiratory tract: is there a role in SARS-CoV-2 infection? Front Physiol. 2021;12:776963. pmid:35002761
  30. 30. Ho FK, Celis-Morales CA, Gray SR, Katiireddi SV, Niedzwieds CL, Hastie C, et al. Modifiable and non-modifiable risk factors for COVID-19, and comparison to risk factors for influenza and pneumonia: results from a UK Biobank prospective cohort study. BMJ Open 2020;10(11):e040402. pmid:33444201
  31. 31. Zhang K, Dong S-S, Guo Y, Tang S-H, Wu H, Yao S, et al. Causal associations between blood lipids and COVID-19 risk: A two-sample Mendelian randomization study. Arterioscl Thromb Vasc Biol. 2021;41:2802–10. pmid:34496635
  32. 32. Okorodudu DO, Jumean MF, Montori VM, Romero-Corral A, Somers VK, Erwin PJ et al (2010) Diagnostic performance of body mass index to identify obesity as defined by body adiposity: a systematic review and meta-analysis. Int J Obes 34:791–9. pmid:20125098
  33. 33. Malavazos AE, Secchi F, Basilico S, Capitanio G, Boveri S, Milani V, et al. Abdominal obesity phenotype is associated with COVID-19 chest X-ray severity score better than BMI-based obesity. Eat Weight Disord. 2021. pmid:33821453
  34. 34. Christensen RAG, Sturrock SL, Arneja J, Brooks JD. Measures of adiposity and risk of testing positive for SARS-CoV-2 in the UK Biobank Study. J Obesity. 2021;2021:8837319. pmid:33542836
  35. 35. Freuer D, Linseisen J, Meisinger M. Impact of body composition on COVID-19 susceptibility and severity: A two-sample multivariable Mendelian randomization study. Metabolism. 2021;118:154732. pmid:33631142
  36. 36. Hoffmann M, Kleine-Weber H, Schroeder S, Krüger N, Herrler T, Erichsen S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell. 2020;181:271–80. pmid:32142651
  37. 37. Al-Benna S. Association of high level gene expression of ACE2 in adipose tissue with mortality of COVID-19 infection in obese patients. Obes Med. 2020;19:100283. pmid:32835126
  38. 38. Jia X, Yin C, Lu S, Chen Y, Liu Q, Bai J, et al. Two things about COVID-19 might need attention. Preprints 2020, 2020020315.
  39. 39. Bayati A, Kumar R, Francis V, McPherson PS. SARS-CoV-2 infects cells after viral entry via clathrin-mediated endocytosis. J Biol Chem. 2021;296: 100306. pmid:33476648
  40. 40. Dang EV, Madhani HD, Vance RE. Cholesterol in quarantine. Nat Immunol. 2020; 21(7):716–7. pmid:32514065
  41. 41. Kocar E, Rezen T, Rozman D. Cholesterol, lipoproteins, and COVID-19: Basic concepts and clinical applications. Biochim Biophys Acta Mol Cell Biol Lipids. 2021;1866:158849. pmid:33157278
  42. 42. Zinellu A, Panagiotis P, Fois AG, Solidoro P, Carru C, Mangoni AA. Cholesterol and triglyceride concentrations, COVID-19 severity, and mortality: A systematic review and meta-analysis with meta-regression. Front Public Health. 2021;9:1210. https://doi.org/10.3389/fpubh.2021.705916.
  43. 43. Fatima Y, Bucks RS, Mamun AA, Skinner I, Rosenzweig I, Leschziner G, et al. Shift work is associated with increased risk of COVID-19: Findings from the UK Biobank cohort. J Sleep Res. 2021;30:e13326. pmid:33686714
  44. 44. Maidstone R, Anderson SG, Ray DW, Rutter MK, Durrington HJ, Blaikley JF. Shift work is associated with positive COVID-19 status in hospitalised patients. Thorax 2021;76:601–6. pmid:33903187