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

Effects of walking impairment on mental health burden, health risk behavior and quality of life in patients with intermittent claudication: A cross-sectional path analysis

  • Farhad Rezvani ,

    Roles Formal analysis, Methodology, Writing – original draft, Writing – review & editing

    f.rezvani@uke.de

    Affiliation Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

  • Mara Pelt,

    Roles Formal analysis, Writing – original draft

    Affiliation Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

  • Martin Härter,

    Roles Funding acquisition, Supervision, Writing – review & editing

    Affiliation Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

  • Jörg Dirmaier

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

    Affiliation Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

Abstract

Introduction

Intermittent claudication is the leading symptom of peripheral artery disease (leg pain when walking). The present study investigates the extent to which walking impairment is associated with health-related quality of life, mental health and health risk behavior.

Methods

A theory-based, cross-sectional path model was empirically examined using pre-intervention baseline data from a multicenter, randomized-controlled trial of patients with intermittent claudication (PAD-TeGeCoach). Data were available from 1 696 patients who completed a battery of questionnaires between April 14, 2018 and March 12, 2019, including measures of walking impairment (Walking Impairment Questionnaire), health-related quality of life (SF-12), mental burden (GAD-7, PHQ-9), nicotine- and alcohol-related risk behavior (Fagerström-Test, AUDIT-C). Sociodemographic characteristics and comorbid conditions were included in the postulated model a priori to minimize confounding effects.

Results

Walking impairment was associated with an increase in depressive (β = -.36, p < .001) and anxiety symptoms (β = -.24, p < .001). The prevalence of depressive and anxiety symptoms was 48.3% and 35.5%, respectively, with female patients and those of younger age being at greater risk. Depressive symptoms were predictive of an increased tobacco use (β = .21; p < .001). Walking impairment had adverse effects on physical quality of life, both directly (β = .60, p < .001) and indirectly mediated through depressive symptoms (β = -.16, p < .001); and indirectly on mental quality of life mediated through depressive (β = -.43, p < .001) and anxiety symptoms (β = -.35, p < .001).

Discussion

The findings underscore the need for a comprehensive treatment strategy in patients with intermittent claudication. Measures to improve walking impairment (e.g. exercise training) are key to enhance quality of life and should be the primary treatment. As a key mediator of mental quality of life, depressive and anxiety symptoms should be addressed by rigorously including mental health treatment. Risky health behaviors should be approached by promoting behavior change (e.g. smoking cessation) as a secondary prevention of peripheral artery disease.

Introduction

Peripheral Artery Disease (PAD) affects up to 240 million people worldwide and ranks as the third leading cause of atherosclerotic morbidity after coronary artery disease and stroke [1], making it one of the leading causes of disability [24]. The hallmark symptom in symptomatic PAD patients is Intermittent Claudication (IC), which is characterized by muscle pain in the legs during walking and which subsides with short periods of rest [5]. Confronted with walking impairment and reduced mobility, these symptoms reflect the progressive narrowing of the peripheral arteries and the resulting reduction of blood supply [6, 7] that, if left untreated, can result in amputation [8] and death [9].

There is growing evidence that psychosocial factors are linked to functional outcomes and play a substantial role in the pathogenesis of PAD [10]. Depressive and anxiety symptoms are highly prevalent among PAD patients [1113], which in turn have been shown to be associated with poor walking ability [1418] and severe leg symptoms (i.e. pain at rest) [12], putting PAD patients at greater (long term) risk for mortality and other adverse PAD events [1317, 1922]. Prior studies have also demonstrated the negative impact of PAD and IC symptoms on health-related quality of life (HRQoL) [2326], which again was found to have prognostic value in predicting long-term survival in PAD patients [27]. Experiencing depressive symptoms are associated with significantly lower HRQoL compared with their non-depressed counterparts, highlighting the impact of mental health symptoms on the PAD patient’s subjective appraisal of their health status [28, 29].

While the association of mental health status with PAD is well established, an important next step is to understand the underlying mechanisms (and directionality) to allow targeted interventions. Although still subject of vigorous debate [10], several potential behavioral mediators have been proposed; one of them, tobacco smoking, which is known as a potent risk factor for developing PAD, was also found to be a important factor in the relationship between depression and subsequent PAD events [19]. Likewise, mental distress has been reported to be associated with increased amounts of alcohol consumption [30], which in turn has been identified as a risk factor for PAD [3136]. Overall, the current evidence indicates risky health behaviors as a pathway through which mental health burden is causing poor PAD outcomes [10].

The present study addresses several important questions for the psychosocial management of symptomatic PAD, with the goal to determine whether and how walking impairment is associated with diminished HRQoL and mental burden in PAD patients that suffer from IC. With increased interest in health status and patient-based measures in cardiovascular research, identifying their respective determinants is increasingly important. Furthermore, this study also investigates the impact of mental health problems (i.e. depressive and anxiety symptoms) with risky health behaviors (i.e. alcohol and tobacco consumption), which in the long-term could be major drivers of a negative clinical PAD course [10]. A theory-driven, cross-sectional path model based on previous literature was therefore postulated (Fig 1) and empirically examined to explore the interrelationships among these constructs. The postulated model assumed an association between walking impairment and mental health burden (i.e. depressive and anxiety symptoms; Hypothesis 1), which in turn is linked to an increase in health risk behavior (i.e. tobacco smoking and alcohol drinking; Hypothesis 2). Moreover, walking impairment was hypothesized to have a direct, negative effect on physical HRQoL (Hypothesis 3) and an indirect, negative effect on mental HRQoL mediated by an increase of depressive and anxiety symptoms (Hypothesis 4). A better understanding of these relationships may foster the development of treatment strategies to improve HRQoL and emotional well-being in PAD patients, which may also indirectly have secondary benefits on PAD status.

thumbnail
Fig 1. Theory-based path analysis model regarding the influence of walking impairment on mental burden, health risk behavior, physical and mental HRQoL in PAD patients.

https://doi.org/10.1371/journal.pone.0273747.g001

Methods

Design

The present path analysis uses cross-sectional baseline data (i.e. pre-intervention) drawn from a larger data set that was collected as part of a multicenter, randomized-controlled trial (RCT) designed to test the effectiveness of a 12-month long telemedicine-guided home-based exercise program for patients with IC, PAD-TeGeCoach (CT.gov trial registration: NCT03496948). Methods of the PAD-TeGeCoach effectiveness trial are reported elsewhere in detail [37]. Ethical approval was granted by the ethics committee of the Medical Association of Hamburg. All patients provided written informed consent.

Study population and recruitment

Participants were recruited using routinely collected health insurance data (electronic health records) from three German statutory health insurance funds (in German: Gesetzliche Krankenversicherung): Kaufmännische Krankenkasse, Techniker Krankenkasse, mhplus Krankenkasse. These three statutory health insurance funds together have approx. 12.1 million insured (TK: 10.5 million; KKH: 1.6 million; MH: 0.54 million) and cover 16.5% of all statutory insured citizens in Germany. Consequently, the patient population is likely to represent the PAD patient population presenting in a usual care setting.

Eligible patients were between 35 and 80 years old, and had a medically confirmed diagnosis of PAD at Fontaine stadium IIa (IC > 200 meters) or IIb (IC < 200 meters) within the last 36 months. Patients were excluded from the study if they had asymptomatic PAD within the last 12 months (Fontaine stadium I) or rest pain within the last 36 months (Fontaine stadium III or IV). Patients with active or recent participation in other PAD intervention trials, medical conditions that contradict physical activity, cognitive disorders, severe mental disorders (including a clinical diagnosis of substance use disorder), suicidality, life-threatening illnesses, ongoing hospitalization, and heart failure (NYHA class III/IV) were also excluded.

The study population was derived from the PAD-TeGeCoach RCT; approximately 63 000 who met the inclusion criteria were identified as potential participants and were invited to participate. Of those, 1 982 elected to participate (recruitment rate 3.2%) and were randomized either into the intervention arm or the routine care group (see S1 Fig). There were 11 participants who withdrew after enrollment (data deletion request n = 1, randomized without informed consent n = 1, met exclusion criteria n = 8, lack of verification of PAD diagnosis n = 1).

Measures

The data used for this study (i.e. baseline data from the PAD-TeGeCoach RCT) were collected between April 14, 2018 and March 12, 2019. Enrolled patients received a battery of self-administered questionnaires by mail (paper-pencil) and were asked to return them using a prepaid envelope. The participants could call the study team when they encountered problems completing the questionnaires. A total of 1 696 patients returned their study questionnaire, which falls within the usual range of mail surveys [38].

IC symptoms: Walking Impairment Questionnaire (WIQ).

The Walking Impairment Questionnaire (WIQ) is a well-established instrument of assessing walking impairment for different degrees of difficulty across three domains: walking distance, walking speed and stair-climbing. Response options for all items comprise a five-point Likert scale ranging from “unable to do” to “no difficulty”. Domain scores are generated by multiplying the score for each item by a weighting factor based on the degree of difficulty and then summing all the products together. Scores are then divided by the maximum score of the respective domain to obtain a percentage score, from 0% (i.e. fully impaired) to 100% (i.e. not impaired). WIQ scores are strongly correlated with maximum walking distance [39, 40], objective measures of walking impairment [41], as well as the ankle-brachial index [42].

Generic HRQoL: SF-12.

The SF-12 is a self-assessment questionnaire with 12 items measuring generic HRQoL [43]. The instrument covers eight health domains: physical functioning, role limitations due to physical health problems, bodily pain, general health, vitality, social functioning, role limitations due to emotional problems and mental health. These domains result in two summary measure scores: Physical Component Summary and the Mental Component Summary. Summary measure scores range from 0 (lowest HRQoL) to 100 (highest HRQoL). The SF-12 is a short version of the SF-36 with good psychometric properties [43]. The SF-12 has been used extensively in both cross-sectional and longitudinal PAD studies to assess (changes in) health status [e.g. 44, 45]. The Mental Component Summary score of the SF-12 was shown to be a valid measure of mental health in the general population [46, 47]. Furthermore, the Physical Component Summary score is associated with PAD severity as measured by the ankle-brachial index [45].

Depressive symptoms: PHQ-9.

The PHQ-9 is a depression symptom screening instrument with 9 items asking patients how much they were bothered by symptoms over the last two weeks, with scores on a 4-point scale from ‘not at all’ to ‘nearly every day’. The sum score ranges from 0 to 27 and indicates the degree of depression. Scores of ≥ 5, ≥ 10, and ≥ 15 represent mild, moderate, and severe levels of depression, respectively. A cut-off score of ≥ 10 was found to have a sensitivity and specificity of 0.88 for detecting clinical depression [48].

Anxiety symptoms: GAD-7.

The GAD-7 is a 7-item screening instrument assessing the core symptoms of generalized anxiety disorder (GAD) over the past two weeks. The answer options are identical to the PHQ-9, with scores on a 4-point scale from 0 (‘not at all’) to 3 (‘nearly every day’). The sum score ranges from 0 to 21 with cut-off scores of 5, 10 and 15 representing mild, moderate and severe levels of anxiety, respectively. A cutoff score of ≥ 10 has a sensitivity of 89% and a specificity of 82% for identifying GAD [49]. A study conducted in the German general population confirmed the instrument’s good psychometric properties [50].

Tobacco smoking: Fagerström Test.

The Fagerström Test for Nicotine Dependence [51] is a screening instrument assessing nicotine dependence with respect to cigarette smoking. It consists of six items which are either scored from 0 to 3 (multiple choice items) or 0 to 1 (yes/no items). The sum score ranges from 0 to 10 with higher scores indicating more intense tobacco dependence. The FTND is a revised version of the Fagerström Tolerance Questionnaire (FTQ) [52] with equally good psychometric properties [53]. The Fagerström Test was completed only by those who identified themselves as smokers (n = 668).

Alcohol consumption: AUDIT-C.

The Alcohol Use Disorders Identification Test-Consumption [54] is a short screening instrument consisting of the original AUDIT’s first three items assessing alcohol consumption. Items are scored on a scale ranging from 0 to 4. As a result, the sum score ranges from 0 to 12. Cut-off scores of 3 and 4 are used for women and men to identify patients at increased risk for alcohol-related disorders, whereas a cut-off score of 4 or 5 indicates risky consumption. Research confirmed the validity of the AUDIT-C and found equally good psychometric properties in the AUDIT-C as in the original version [55].

Other measures.

Along with patient-reported outcome measures (PROMs), sociodemographic and biological variables (age, sex, height, weight, body mass index, education level, household income/economic status, marital status and employment status) and comorbidities (hyperlipidemia, diabetes mellitus, hypertension, lung disease and reduced kidney function) were self-reported during the baseline assessment.

Statistical analyses

Secondary analyses were performed using cross-sectional baseline data from a parent RCT (i.e. before study interventions were implemented; S1 Fig). Missing data in PROM items (i.e. incomplete information collected from a respondent) were handled via the Expectation-Maximization (EM) imputation algorithm in IBM SPSS Statistics 25, which is an effective and straightforward maximum likelihood technique to manage incomplete data so that there was be no systematic losses of participants who missed single items [56]. EM is recommended to be used in structural equation modeling [57]. An EM estimator is unbiased and efficient when the missing mechanism is missing completely at random or missing at random [58]. Moreover, the EM algorithm is effective when variables had up to 30% missing values. Consequently, participants that had an item nonresponse of > 30% were removed from the analysis dataset (n = 9). Accordingly, data from 1 687 PAD patients were used for this study. In addition, several PROMs were compared against normative data, which were available from previous studies (GAD-7 [50]; PHQ-9 [59, 60]; SF-12 [61]).

Taking consideration of existing literature, a theory-driven path analysis with full information maximum likelihood estimation was conducted to estimate the simultaneous interrelationships between the variables of interest (treated as continuous), while adjusting a priori for empirically identified confounders (i.e. in path models at p < .05: sociodemographic variables, body mass index, comorbidities). Path analysis, which is an extension of multiple regression analysis, is a type of structural equation modeling to clarify (potentially causal) relationships between the variables assessed. The absolute and relative goodness of fit of the models were assessed based on standard measures of fit; the CMIN/DF statistic (i.e. normed chi-square), the Tucker–Lewis index (TLI), the comparative fit index (CFI), and the root mean square error of approximation (RMSEA). CMIN/DF < 3 indicates an acceptable fit between hypothetical model and sample data [62]. The cut-off for good fit for TLI and CFI is ≥ 0.95 and ≥ 0.90. With values closer to 0 representing good fit, the cut-off for RMSEA, which is an absolute measure of fit, is < .08, indicating excellent fit between model specification and the observed data [63, 64]. Based on model fit indicators, the original model was modified by iteratively including and/or constraining paths and correlations. To arrive at a good model fit, model substructures were assessed based on (standardized) regression weights (i.e. magnitude and p < .05), residual error covariance and modification indices. Several iterations were carried out to arrive at the final revised model. Statistical analyses were performed using IBM SPSS Statistics 25 and SPSS Amos (IBM Corporation, Armonk, New York, United States). Effect sizes (i.e. magnitude of the relationships between path model parameters) were based on Pearson’s r correlation coefficients and the standardized beta coefficient (β), with small, medium and large effect sizes indicated by the following r’s/ β’s, respectively: .10, .30, .50. Effect sizes < .10 are considered negligible regardless of statistical significance in order to avoid possible overinterpretation of small effects.

Results

Study sample characteristics

Demographic, socioeconomic and clinical characteristics of the study sample are displayed in Table 1. Most patients were male (67.6%) with a mean age of 66.3 years (SD = 8.6 years; range: 35–81). 64.3% were married, and 81.6% had at least one child. The three most common self-reported comorbidities were hypertension (72.4%), high cholesterol (57.1%) and diabetes mellitus (25.9%). A number of patients had a history of a cardiovascular event; 12.9% of PAD patients suffered from a myocardial infarction (i.e. heart attack), 8.8% had a stroke in the past. Most patients received medication to help control their PAD and cardiovascular comorbidities, such as platelet function inhibitors (81.1%), antihypertensive agents (74.1%) or statins (58.2%). 29.5% underwent revascularization surgery.

Descriptive statistics

Mental burden.

The estimated proportion of patients with mild depressive symptoms (PHQ-9 score 5–9) was 30.2% (n = 509). Moderate or severe depressive symptoms, which has been reported to indicate clinical depression, were found in 18.1% (n = 304) of patients (PHQ-9 score ≥ 10). Mild anxiety symptoms (GAD-7 score 5–9) were found in 25.8% (n = 435) of patients, while 9.7% (n = 164) had moderate to severe anxiety symptoms (GAD-7 score ≥ 10) and thus showed signs of clinical anxiety. Compared to the general German population [50, 59, 60], the study population showed substantially higher levels of depression (approx. 84th percentile), and anxiety symptoms (approx. 69th percentile).

Health risk behavior.

Among the smokers subgroup (n = 668, 39.6% of study participants), low or moderate level of tobacco dependence (Fagerström score 0–4) was identified in 56.3% of patients (n = 376, 22.3% of study participants). The estimated proportion of patients with high or very high tobacco dependence among smokers (Fagerström score 5–10) was 43.7% (n = 292, 17.3% of study participants). Regarding alcohol use, 16.1% (n = 272) were at risk of alcohol-related disorder (AUDIT-C score = 3 in women; = 4 in men), while 29.1% (n = 491) were screened positive for risky consumption (AUDIT-C score ≥ 4 in women; ≥ 5 in men).

HRQoL.

In comparison to the non-clinical German population [61], physical aspects of HRQoL among PAD patients appeared to be severely impaired (approx. 17th percentile; SF-12 physical composite score: M = 37.92, SD = 9.78), whereas mental aspects of HRQoL were only mildly compromised (approx. 45th percentile; SF-12 mental composite score M = 51.03, SD = 11.18).

Path analysis

Original and revised model through respecification.

A theory-driven path analysis (Fig 2) was performed to evaluate the interrelationships between walking impairment (WIQ), HRQoL (SF-12 mental and physical composite scores), health risk behavior (AUDIT-C; Fagerström-Test) and mental health measures (GAD7; PHQ9). The original model failed to show a sufficiently good fit (CMIN/DF = 10.223; TLI = .942; CFI = .981; RMSEA = .074). As a next step, the model was controlled for potentially confounding effects (i.e. sociodemographic factors, body mass index, comorbidities) and respecified accordingly; goodness-of-fit indices indicated to include age and sex as confounders (represented by grey lines in Fig 2). After controlling for confounding effects, the goodness-of-fit indices showed a better fit to the observed data (CMIN/DF = 7.506; TLI = .939; CFI = .982; RMSEA = .062). Modification indices and residual variances indicated to add one path to the original model, as represented by a red line in Fig 2, which further improved the overall model fit (CMIN/DF = 2.743; TLI = .984; CFI = .996; RMSEA = .032). As a last step, two paths and one error covariance that were not significant were constrained to 0 (represented by thin lines in Fig 2). The results from all model iterations are presented in S2 File. Following these iterations, the goodness-of-fit indices showed an excellent fit between the observed data and the revised model (CMIN/DF = 2.345; TLI = .987; CFI = .996; RMSEA = .028). The final revised model, with accompanying path coefficients (i.e. standardized regression weights) and squared multiple correlations, is presented in Fig 2. The results of the decomposition of effects based on the path analysis model are shown in Table 2.

thumbnail
Fig 2. Final path analysis model testing the influence of walking impairment on mental burden, health risk behavior, physical and mental HRQoL in PAD patients (N = 1 687).

The numbers on the arrows are standardized regression coefficients (β) that indicate the magnitude of effects between variables (coefficients < .10 not shown). Pathways are represented by thick lines, pathways that were constrained to 0 due to model respecification are represented by thin lines. Grey lines represent added covariates to the model (i.e. age, sex) for adjustment of confounding (coefficients not shown; see Table 2). The numbers above the boxes indicate the total proportion of variance explained in the model (R2).

https://doi.org/10.1371/journal.pone.0273747.g002

thumbnail
Table 2. Decomposition of direct effects from the path analysis (Regression and error covariances).

https://doi.org/10.1371/journal.pone.0273747.t002

Walking impairment, mental health burden and health risk behavior.

Limitations due to IC symptoms were associated with an overall increase in mental burden; in the model, walking impairment had a moderate direct effect on depressive symptoms (β = -.36) and, to a lesser extent, on anxiety symptoms (β = -.24). The model explained 19% and 13% of the variance in depressive and anxiety symptoms, with age and sex accounting for a large portion of the total explained variance (Table 2).

Depressive symptoms, in turn, had a small to moderate direct effect on the amount of tobacco smoking (β = .21), while anxiety symptoms had a negligible direct effect on alcohol drinking (β = -.06). The model explained 12% and 9% of the variance in tobacco and alcohol use, but again with age and sex accounting for the large portion of the explained variance. The indirect effects of walking impairment on tobacco and alcohol use mediated through mental health burden (i.e. depressive and anxiety symptoms) are considered negligible (total indirect β’s < .10).

Walking impairment on health-related quality of life.

Walking impairment had a large direct effect on lower physical HRQoL (β = .60). In addition, walking impairment was also substantially predictive of lower mental HRQoL, although fully mediated by an increase in depressive and anxiety symptoms (total indirect β = .24). Overall, the model explained 45% and 55% of the variance in physical and mental HRQoL.

Discussion

Mental health

The descriptive results show that patients with PAD are at much higher risk of presenting depressive symptoms compared with the general population [59, 60]. The reported prevalence is in good agreement with previous studies [17]; for instance, depression or depressive symptoms have been observed in 16% [14], 19.6% [13], 21.7% [15], 24% [65], 30% [12], up to 36.1% shortly before revascularization [66], compared to 48.3% showing at least mild depressive symptoms in this study, and of these, 18.1% showings signs of clinical depression (PHQ-9 score > = 10). Finally, results from the path model confirm that young female PAD patients are at modestly higher risk to develop depressive symptoms [17, 29, 67, 68].

Moreover, the path analysis results support the hypothesis that poor walking ability contributes to depressive symptoms [1417, 65, 69]. These findings support previous studies that show an association between PAD outcomes and depressive symptoms. PAD patients suffering from depressive symptoms are more likely to have other clinical symptoms such as chest discomfort, shortness of breath, and heart palpitations [15]. In addition, comorbid depressive symptoms are associated with an increased risk of PAD events [19], secondary cardiovascular events [22], major amputations [20, 70] and mortality [13]. Finally, PAD patients with depressive symptoms are less willing to exercise [69] and more likely to have recurrent symptoms after revascularization [66], which may further aggravate PAD symptoms. Although the current indicate a single direction of effect, the relationship between depression and PAD outcomes has been hypothesized to be bi-directional in a mutually reinforcing cycle, meaning that PAD outcomes are thought to increase depression and vice versa [71].

The body of literature examining other mental health issues in PAD patients is limited, as much of the literature tends to focus on the relationship between depression and PAD. That being said, the descriptive results show that PAD patients are also at much higher risk of having comorbid anxiety symptoms compared with the general population [50]. Anxiety symptoms were observed in 35.6%, which is comparable to 30% [12] and 24.4% [11] in other studies. The path analysis results support the hypothesis that poor walking ability contributes to anxiety symptoms. As for depression, it is reasonable to assume that anxiety disorders and PAD outcomes are also in a bidirectional relationship, as anxiety has been previously identified as a risk factor for the development of IC [18] and is associated with severe leg symptoms (i.e. pain at rest) [12]. Furthermore, it was shown that anxiety enhances the detrimental effect of depressive symptoms on health status after revascularization [72]. Future studies should further explore this association and whether tailored mental health interventions would improve PAD outcomes.

Health risk behavior

The descriptive results also demonstrate that PAD patients, especially men of younger age, are at great risk of engaging in health risk behavior such as tobacco use and excessive alcohol consumption. In the present study, 45.2% of patients were identified to be at risk of an alcohol-related disorder or exhibit risky alcohol consumption, compared to 39% found in a previous study [73]. Additionally, 39.6% of PAD patients were identified as smokers. Other research investigating home-based exercise programs in PAD patients reported smoking frequencies ranging from as little as 21.4% [44] up to 86.1% [74], suggesting a considerable heterogeneity between studies. Such health risk behavior can cause profound damage to vascular health. In particular, tobacco use is the single most important cause and leading risk factor of PAD [3] with a threshold- [75], dose-response-relationship [76], fostering progression of functional impairment [77, 78] and thereby resulting in a reduced HRQoL [78]. In terms of alcohol consumption, a U- or J-shape dose-response relationship between alcohol use and PAD has been suggested in various studies, meaning that low-to-moderate alcohol consumption, (particularly of red wine [79]) may result in a reduction of cardiovascular events and mortality [3234, 80], while heavy/risky drinking is severely detrimental to PAD [3136].

Mounting evidence suggests that risky health behaviors are part of the underlying mechanistic link between mental health status and PAD outcomes [10]. The path analysis results support the hypothesis that mental distress results in an increased desire to smoke among PAD patients [19], which in turn may contribute to the pathogenesis and deterioration of PAD. Regardless of PAD status, smoking is generally suggested as a self-medication strategy to cope with mental distress [81, 82]. However, there is evidence of a bidirectional relationship between depression and smoking, in which depressive symptoms lead to self-medication by smoking, which in turn causes changes in the dopaminergic system leading to depressed mood [82]—a vicious that eventually leads to a further deterioration of PAD.

One unanticipated result of the study was that mental burden was not associated with an increase in alcohol use. In the general population, the current literature suggests a causal linkage of alcohol use increasing the risk for depression, while alcohol being used to self-medicate symptoms of depression to reduce emotional distress [83]. These findings cannot be confirmed for PAD patients, suggesting that alcohol use plays no major role in the mechanistic relationship between mental distress and negative PAD outcomes. However, it is important to note that patients with a clinically diagnosed affective and/or substance use disorder were excluded from the study, which may have affected the current results. It is possible that severely depressed patients and those suffering severely from anxiety are more likely to show stronger signs of alcohol use disorder [84], which however remains to be investigated in further studies.

HRQoL

Compared to the general population, PAD patients were also found to have an impaired HRQoL, which is largely consistent with previous studies that have demonstrated poor HRQoL in PAD patients [45, 85, 86]. Similar to previous studies [23, 24, 45, 85], lower HRQoL was more evident for the physical aspects of HRQoL.

Moreover, in accordance with previous findings [2326], the current path analysis support the hypothesis that poor HRQoL is largely related to increasing walking impairment. For mental HRQoL, this effect was largely mediated by the PAD patient’s magnitude of depressive and anxiety symptoms, which highlights that the reduction of HRQoL is to large extent due to IC’s detrimental effect on mental health [46]. The detrimental effect of mental health on HRQoL measures has been well demonstrated in previous studies [28, 29]. Similarly, in patients with chronic heart failure, depression predicted physical and mental aspects of HRQoL [87]. Notably, these effects were independent of other physically debilitating comorbidities that also have an impact on patients’ HRQoL (e.g. lung diseases).

Implications for clinical practice

The path analysis results provide a reasonable explanation of the complex interaction between functional walking limitations, mental burden, health risk behavior and quality of life in PAD patients, holding important clinical and public health implications. First and foremost, improving IC symptoms is a vital treatment approach for PAD patients, since walking impairment was found to be a crucial determinant of mental burden and HRQoL. Because the improvement of HRQoL is a key therapeutic goal in the treatment of PAD patients, staying physically active with appropriate exercise programs and other treatment modalities to improve walking impairment (e.g. revascularization) remains an integral key part of PAD treatment. The secondary benefits of walking improvement on HRQoL through exercise therapy is well established [8890]. Importantly, to monitor changes in walking impairment as a result of treatment, the treating clinicians should use patient-reported measures of functional disability [25, 26], as these are the primary predictor of HRQoL [25, 26]. In contrast, HRQoL in PAD patients is only marginally associated with clinical markers as well as objective measurements of walking impairment [9193], or HRQoL assessments of physicians [94], suggesting that the experience of HRQoL is not fully reflected by these surrogate measures. The importance of HRQoL, reflecting the physical, social and mental well-being of PAD patients, is being increasingly recognized by physicians and stakeholders (patients, relatives, etc.) as a significant indicator of treatment success [95, 96], which is nowadays also acknowledged in several international guidelines [5, 97, 98].

Second, the presence of mental health issues has been related to adverse health outcomes and influences the prognosis and treatment response of PAD, which points to the importance of integrating psychological aspects into therapy conversations. To break the self-perpetuating circle between mental health burden and PAD progression (i.e., amputation, cardiovascular events) [1317, 1922], vascular care providers should pay close attention to mental health challenges of PAD patients by integrating mental health care providers in an interdisciplinary/collaborative care model [17], which likely would have secondary benefits in reducing PAD risk and improving HRQoL. In patients with corona artery disease, previous studies have demonstrated the positive impact of depression and anxiety care and stress management on cardiovascular and psychological outcomes [99101]. Likewise, the treatment of depressive symptoms improve physical functioning in older adults [102], which should therefore be considered a viable therapeutic approach in the management of PAD. Remarkably, there is already a guideline on addressing depression for patients with coronary artery disease [103], recommending to use the PHQ-9 to screen for depression, but not yet for PAD, which should be urgently addressed in the near future as psychosocial stressors play a critical role in PAD development and progression. For instance, psychological distress [104], including work-related stress [105], was found to elevate the risk for PAD and show a poor PAD recovery pathway [29].

Third, reducing health risk behavior should always be a key target of PAD management for effectively reducing adverse PAD outcomes, as tobacco and excessive alcohol use are known to be potent factors in the development and progression of PAD. Changes in health risk behavior should be also addressed through the delivery of PAD lifestyle interventions ([106], e.g. smoking cessation programs), which are usually guided by conceptual frameworks for risk behavior modification (for an overview, see [107]). The use of lifestyle interventions is currently low, although they have substantial secondary cardiovascular benefits and may prevent further worsening of PAD [106]. Finally, it has been speculated that depressed patients use smoking as a form of self-medication to relieve symptoms; accordingly, modifying risk health behaviors could be achieved by improving mental health. In fact, there is good evidence that psychological interventions are effective in reducing smoking by people with mental health problems [108], which may in turn have a beneficial effect on the patient’s PAD status and HRQoL.

Limitations

Several potential limitations must be mentioned when interpreting the findings of this study. Since all measures were collected cross-sectional, no certain conclusions can be drawn about temporal and causal relationships. Therefore, the directional arrows in the path analysis should be interpreted with great caution, as path analysis cannot prove causality out of a cross-sectional study (which can be proven only through the correct research design), but rather intended to test whether the data are consistent with the postulated causal model based on theoretical considerations. With that said, the current models can help to generate causal hypotheses for future studies, even more so given the “real-world” setting of this study with a study sample that is highly representative of PAD patients with IC.

Furthermore, despite the largely theory-driven approach, it is important to treat some of the results with caution, as some of them show trivial effect sizes although being statistically significant. For path analysis, an adequate sample size should normally be ten times the amount of the parameters as a rule of thumb, whereas in this study the sample is almost 200 times higher, which increases the power of detecting very small effects resulting in statistical significance. Although larger studies such as this one are unquestionably valuable and generally viewed as a favorable development, with all parameter values estimated with higher accuracy, it is important to consider how clinically and practically ‘relevant’ these effects really are in relation to prior literature. Therefore, to avoid an overinterpretation of effects (‘large sample size fallacy’), it is important to interpret all effects in the model appropriately according to their size, and not treat statistical significance synonymously with practical significance [109]. At the same time, the large sample size can be regarded as a strength of the study, as the current findings comprise robust evidence and are most likely not caused by a statistical artifact.

Conclusions

In conclusion, the present results demonstrate that PAD patients often experience substantial impairment in terms of functional health status, mental burden and HRQoL. In order to better understand the complex relationship between these factors, the study sought to integrate clinical indicators and psychosocial aspects of PAD into a single theoretical model, thereby supporting a more comprehensive, multimodal therapeutic approach to PAD. The findings clearly indicate the importance of not only including somatic health status in the treatment of PAD, but also accounting for psychosocial aspects in PAD. To expand the explanatory ability of the complex relationships in the field of PAD, future research should put greater efforts in a theory-based approach using more sophisticated multivariate data analysis techniques (e.g. structural equation models) that defines the entire set of relationships.

Supporting information

S1 Fig. Flow chart of the randomized-controlled trial.

https://doi.org/10.1371/journal.pone.0273747.s001

(TIF)

S1 File. All relevant study data (SPSS file).

https://doi.org/10.1371/journal.pone.0273747.s002

(SAV)

Acknowledgments

We would like to thank Finja Mäueler, who assisted us with great enthusiasm and commitment in the preparation of the manuscript.

References

  1. 1. Fowkes FG, Rudan D, Rudan I, Aboyans V, Denenberg JO, McDermott MM, et al. Comparison of global estimates of prevalence and risk factors for peripheral artery disease in 2000 and 2010: a systematic review and analysis. Lancet. 2013;382(9901):1329–40. pmid:23915883
  2. 2. Criqui MH, Aboyans V. Epidemiology of peripheral artery disease. Circ Res. 2015;116(9):1509–26. pmid:25908725
  3. 3. Song P, Rudan D, Zhu Y, Fowkes FJI, Rahimi K, Fowkes FGR, et al. Global, regional, and national prevalence and risk factors for peripheral artery disease in 2015: an updated systematic review and analysis. Lancet Glob Health. 2019;7(8):e1020–e30. pmid:31303293
  4. 4. Sampson UK, Fowkes FG, McDermott MM, Criqui MH, Aboyans V, Norman PE, et al. Global and regional burden of death and disability from peripheral artery disease: 21 world regions, 1990 to 2010. Glob Heart. 2014;9(1):145–58.e21. pmid:25432124
  5. 5. Gerhard-Herman MD, Gornik HL, Barrett C, Barshes NR, Corriere MA, Drachman DE, et al. 2016 AHA/ACC guideline on the management of patients with lower extremity peripheral artery disease: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2017;135(12):e686–e725. pmid:27840332
  6. 6. Hamburg NM, Creager MA. Pathophysiology of Intermittent Claudication in Peripheral Artery Disease. Circ J. 2017;81(3):281–9. pmid:28123169
  7. 7. Hiatt WR, Armstrong EJ, Larson CJ, Brass EP. Pathogenesis of the limb manifestations and exercise limitations in peripheral artery disease. Circ Res. 2015;116(9):1527–39. pmid:25908726
  8. 8. Anand SS, Caron F, Eikelboom JW, Bosch J, Dyal L, Aboyans V, et al. Major Adverse Limb Events and Mortality in Patients With Peripheral Artery Disease: The COMPASS Trial. J Am Coll Cardiol. 2018;71(20):2306–15. pmid:29540326
  9. 9. Agnelli G, Belch JJF, Baumgartner I, Giovas P, Hoffmann U. Morbidity and mortality associated with atherosclerotic peripheral artery disease: A systematic review. Atherosclerosis. 2020;293:94–100. pmid:31606132
  10. 10. Ramirez JL, Drudi LM, Grenon SM. Review of biologic and behavioral risk factors linking depression and peripheral artery disease. Vasc Med. 2018;23(5):478–88. pmid:29801423
  11. 11. Aragao JA, de Andrade LGR, Neves OMG, Aragao ICS, Aragao FMS, Reis FP. Anxiety and depression in patients with peripheral arterial disease admitted to a tertiary hospital. J Vasc Bras. 2019;18:e20190002. pmid:31488975
  12. 12. Smolderen KG, Hoeks SE, Pedersen SS, van Domburg RT, L II de, Poldermans D. Lower-leg symptoms in peripheral arterial disease are associated with anxiety, depression, and anhedonia. Vasc Med. 2009;14(4):297–304. pmid:19808714
  13. 13. McDermott MM, Guralnik JM, Tian L, Kibbe MR, Ferrucci L, Zhao L, et al. Incidence and Prognostic Significance of Depressive Symptoms in Peripheral Artery Disease. J Am Heart Assoc. 2016;5(3):e002959. pmid:26994131
  14. 14. Smolderen KG, Aquarius AE, de Vries J, Smith OR, Hamming JF, Denollet J. Depressive symptoms in peripheral arterial disease: a follow-up study on prevalence, stability, and risk factors. J Affect Disord. 2008;110(1–2):27–35. pmid:18237784
  15. 15. Mc Dermott MM, Greenland P, Guralnik JM, Liu K, Criqui MH, Pearce WH, et al. Depressive symptoms and lower extremity functioning in men and women with peripheral arterial disease. J Gen Intern Med. 2003;18(6):461–7. pmid:12823653
  16. 16. Ruo B, Liu K, Tian L, Tan J, Ferrucci L, Guralnik JM, et al. Persistent depressive symptoms and functional decline among patients with peripheral arterial disease. Psychosom Med. 2007;69(5):415–24. pmid:17556643
  17. 17. Brostow DP, Petrik ML, Starosta AJ, Waldo SW. Depression in patients with peripheral arterial disease: A systematic review. Eur J Cardiovasc Nurs. 2017;16(3):181–93. pmid:28051339
  18. 18. Bowlin SJ, Medalie JH, Flocke SA, Zyzanski SJ, Goldbourt U. Epidemiology of intermittent claudication in middle-aged men. Am J Epidemiol. 1994;140(5):418–30. pmid:8067334
  19. 19. Grenon SM, Hiramoto J, Smolderen KG, Vittinghoff E, Whooley MA, Cohen BE. Association between depression and peripheral artery disease: insights from the heart and soul study. J Am Heart Assoc. 2012;1(4):e002667. pmid:23130170
  20. 20. Arya S, Lee S, Zahner GJ, Cohen BE, Hiramoto J, Wolkowitz OM, et al. The association of comorbid depression with mortality and amputation in veterans with peripheral artery disease. J Vasc Surg. 2018;68(2):536–45.e2. pmid:29588133
  21. 21. Wattanakit K, Williams JE, Schreiner PJ, Hirsch AT, Folsom AR. Association of anger proneness, depression and low social support with peripheral arterial disease: the Atherosclerosis Risk in Communities Study. Vasc Med. 2005;10(3):199–206. pmid:16235773
  22. 22. Cherr GS, Zimmerman PM, Wang J, Dosluoglu HH. Patients with depression are at increased risk for secondary cardiovascular events after lower extremity revascularization. J Gen Intern Med. 2008;23(5):629–34. pmid:18299940
  23. 23. Dumville JC, Lee AJ, Smith FB, Fowkes FG. The health-related quality of life of people with peripheral arterial disease in the community: the Edinburgh Artery Study. Br J Gen Pract. 2004;54(508):826–31. pmid:15527608
  24. 24. Breek JC, Hamming JF, De Vries J, Aquarius AE, van Berge Henegouwen DP. Quality of life in patients with intermittent claudication using the World Health Organisation (WHO) questionnaire. Eur J Vasc Endovasc Surg. 2001;21(2):118–22. pmid:11237783
  25. 25. Gardner AW, Montgomery PS, Wang M, Xu C. Predictors of health-related quality of life in patients with symptomatic peripheral artery disease. J Vasc Surg. 2018;68(4):1126–34. pmid:29615353
  26. 26. Muller-Buhl U, Engeser P, Klimm HD, Wiesemann A. Quality of life and objective disease criteria in patients with intermittent claudication in general practice. Fam Pract. 2003;20(1):36–40. pmid:12509368
  27. 27. Issa SM, Hoeks SE, Scholte op Reimer WJ, Van Gestel YR, Lenzen MJ, Verhagen HJ, et al. Health-related quality of life predicts long-term survival in patients with peripheral artery disease. Vasc Med. 2010;15(3):163–9. pmid:20483986
  28. 28. Smolderen KG, Safley DM, House JA, Spertus JA, Marso SP. Percutaneous transluminal angioplasty: association between depressive symptoms and diminished health status benefits. Vasc Med. 2011;16(4):260–6. pmid:21828173
  29. 29. Qua Jelani, Mena-Hurtado C, Burg M, Soufer R, Gosch K, Jones PG, et al. Relationship Between Depressive Symptoms and Health Status in Peripheral Artery Disease: Role of Sex Differences. Journal of the American Heart Association. 2020;9(16):e014583. pmid:32781883
  30. 30. Hamer M, Molloy GJ, Stamatakis E. Psychological distress as a risk factor for cardiovascular events: pathophysiological and behavioral mechanisms. J Am Coll Cardiol. 2008;52(25):2156–62. pmid:19095133
  31. 31. Yang S, Wang S, Yang B, Zheng J, Cai Y, Yang Z. Alcohol consumption is a risk factor for lower extremity arterial disease in Chinese patients with T2DM. Journal of diabetes research. 2017;2017. pmid:28761879
  32. 32. Athyros VG, Liberopoulos EN, Mikhailidis DP, Papageorgiou AA, Ganotakis ES, Tziomalos K, et al. Association of Drinking Pattern and Alcohol Beverage Type With the Prevalence of Metabolic Syndrome, Diabetes, Coronary Heart Disease, Stroke, and Peripheral Arterial Disease in a Mediterranean Cohort. Angiology. 2007;58(6):689–97. pmid:18216378
  33. 33. Fernández-Solà J. Cardiovascular risks and benefits of moderate and heavy alcohol consumption. Nature Reviews Cardiology. 2015;12(10):576–87. pmid:26099843
  34. 34. Bell S, Daskalopoulou M, Rapsomaniki E, George J, Britton A, Bobak M, et al. Association between clinically recorded alcohol consumption and initial presentation of 12 cardiovascular diseases: population based cohort study using linked health records. BMJ. 2017;356:j909. pmid:28331015
  35. 35. Burgess S. Alcohol consumption and cardiovascular disease: A Mendelian randomization study. 2020.
  36. 36. Vliegenthart R, Geleijnse JM, Hofman A, Meijer WT, van Rooij FJ, Grobbee DE, et al. Alcohol consumption and risk of peripheral arterial disease: the Rotterdam study. Am J Epidemiol. 2002;155(4):332–8. pmid:11836197
  37. 37. Rezvani F, Heider D, Härter M, König H-H, Bienert F, Brinkmann J, et al. Telephone health coaching with exercise monitoring using wearable activity trackers (TeGeCoach) for improving walking impairment in peripheral artery disease: study protocol for a randomised controlled trial and economic evaluation. BMJ Open. 2020;10(6):e032146. pmid:32503866
  38. 38. Asch DA, Jedrziewski MK, Christakis NA. Response rates to mail surveys published in medical journals. J Clin Epidemiol. 1997;50(10):1129–36. pmid:9368521
  39. 39. Frans FA, Zagers MB, Jens S, Bipat S, Reekers JA, Koelemay MJ. The relationship of walking distances estimated by the patient, on the corridor and on a treadmill, and the Walking Impairment Questionnaire in intermittent claudication. J Vasc Surg. 2013;57(3):720–7.e1. pmid:23313183
  40. 40. Tew G, Copeland R, Le Faucheur A, Gernigon M, Nawaz S, Abraham P. Feasibility and validity of self-reported walking capacity in patients with intermittent claudication. J Vasc Surg. 2013;57(5):1227–34. pmid:23384490
  41. 41. McDermott MM, Liu K, Guralnik JM, Martin GJ, Criqui MH, Greenland P. Measurement of walking endurance and walking velocity with questionnaire: validation of the walking impairment questionnaire in men and women with peripheral arterial disease. J Vasc Surg. 1998;28(6):1072–81. pmid:9845659
  42. 42. Myers SA, Johanning JM, Stergiou N, Lynch TG, Longo GM, Pipinos II. Claudication distances and the Walking Impairment Questionnaire best describe the ambulatory limitations in patients with symptomatic peripheral arterial disease. J Vasc Surg. 2008;47(3):550–5. pmid:18207355
  43. 43. Ware JE Jr, Kosinski M, Keller SD. A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Med Care. 1996;34(3):220–33. pmid:8628042
  44. 44. McDermott MM, Guralnik JM, Criqui MH, Ferrucci L, Zhao L, Liu K, et al. Home-based walking exercise in peripheral artery disease: 12-month follow-up of the GOALS randomized trial. J Am Heart Assoc. 2014;3(3):e000711. pmid:24850615
  45. 45. Wu AZ, Coresh J, Selvin E, Tanaka H, Heiss G, Hirsch AT, et al. Lower Extremity Peripheral Artery Disease and Quality of Life Among Older Individuals in the Community. Journal of the American Heart Association. 2017;6(1):e004519 pmid:28108464
  46. 46. Gill SC, Butterworth P, Rodgers B, Mackinnon A. Validity of the mental health component scale of the 12-item Short-Form Health Survey (MCS-12) as measure of common mental disorders in the general population. Psychiatry Res. 2007;152(1):63–71. pmid:17395272
  47. 47. Vilagut G, Forero CG, Pinto-Meza A, Haro JM, De Graaf R, Bruffaerts R, et al. The mental component of the short-form 12 health survey (SF-12) as a measure of depressive disorders in the general population: results with three alternative scoring methods. Value Health. 2013;16(4):564–73. pmid:23796290
  48. 48. Kroenke K, Spitzer RL. The PHQ-9: A new depression diagnostic and severity measure. Psychiatric Annals. 2002;32(9):509–15.
  49. 49. Spitzer RL, Kroenke K, Williams JB, Lowe B. A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med. 2006;166(10):1092–7. pmid:16717171
  50. 50. Lowe B, Decker O, Muller S, Brahler E, Schellberg D, Herzog W, et al. Validation and standardization of the Generalized Anxiety Disorder Screener (GAD-7) in the general population. Med Care. 2008;46(3):266–74. pmid:18388841
  51. 51. Heatherton TF, Kozlowski LT, Frecker RC, Fagerstrom KO. The Fagerstrom Test for Nicotine Dependence: a revision of the Fagerstrom Tolerance Questionnaire. Br J Addict. 1991;86(9):1119–27.
  52. 52. Fagerström K-O. Measuring degree of physical dependence to tobacco smoking with reference to individualization of treatment. Addict Behav. 1978;3(3–4):235–41. pmid:735910
  53. 53. Pomerleau CS, Carton SM, Lutzke ML, Flessland KA, Pomerleau OF. Reliability of the Fagerstrom tolerance questionnaire and the Fagerstrom test for nicotine dependence. Addict Behav. 1994;19(1):33–9. pmid:8197891
  54. 54. Bush K, Kivlahan DR, McDonell MB, Fihn SD, Bradley KA. The AUDIT alcohol consumption questions (AUDIT-C): an effective brief screening test for problem drinking. Ambulatory Care Quality Improvement Project (ACQUIP). Alcohol Use Disorders Identification Test. Arch Intern Med. 1998;158(16):1789–95. pmid:9738608
  55. 55. Meneses-Gaya C, Zuardi AW, Loureiro SR, Hallak JE, Trzesniak C, de Azevedo Marques JM, et al. Is the full version of the AUDIT really necessary? Study of the validity and internal construct of its abbreviated versions. Alcoholism: Clinical and Experimental Research. 2010;34(8):1417–24. pmid:20491736
  56. 56. Dempster AP, Laird NM, Rubin DB. Maximum likelihood from incomplete data via the EM algorithm. Journal of the Royal Statistical Society: Series B (Methodological). 1977;39(1):1–22.
  57. 57. Hair JF. Multivariate data analysis. 2009.
  58. 58. Dong Y, Peng C-YJ. Principled missing data methods for researchers. SpringerPlus. 2013;2(1):1–17.
  59. 59. Hinz A, Ernst J, Glaesmer H, Brähler E, Rauscher FG, Petrowski K, et al. Frequency of somatic symptoms in the general population: Normative values for the Patient Health Questionnaire-15 (PHQ-15). J Psychosom Res. 2017;96:27–31. pmid:28545789
  60. 60. Kocalevent R-D, Hinz A, Brähler E. Standardization of the depression screener patient health questionnaire (PHQ-9) in the general population. Gen Hosp Psychiatry. 2013;35(5):551–5. pmid:23664569
  61. 61. Wirtz MA, Morfeld M, Glaesmer H, Brähler E. Normierung des SF-12 Version 2.0 zur Messung der gesundheitsbezogenen Lebensqualität in einer deutschen bevölkerungsrepräsentativen Stichprobe. Diagnostica. 2018.
  62. 62. Kline RB. Principles and practice of structural equation modeling: Guilford publications; 2015.
  63. 63. MacCallum RC, Browne MW, Sugawara HM. Power analysis and determination of sample size for covariance structure modeling. Psychol Methods. 1996;1(2):130.
  64. 64. Lt Hu, Bentler PM. Cutoff criteria for fit indexes in covariance structure analysis: Conventional criteria versus new alternatives. Structural equation modeling: a multidisciplinary journal. 1999;6(1):1–55.
  65. 65. Arseven A, Guralnik JM, O’Brien E, Liu K, McDermott MM. Peripheral arterial disease and depressed mood in older men and women. Vasc Med. 2001;6(4):229–34. pmid:11958388
  66. 66. Cherr GS, Wang J, Zimmerman PM, Dosluoglu HH. Depression is associated with worse patency and recurrent leg symptoms after lower extremity revascularization. J Vasc Surg. 2007;45(4):744–50. pmid:17303367
  67. 67. Smolderen KG, Spertus JA, Vriens PW, Kranendonk S, Nooren M, Denollet J. Younger women with symptomatic peripheral arterial disease are at increased risk of depressive symptoms. J Vasc Surg. 2010;52(3):637–44. pmid:20576397
  68. 68. Grenon SM, Cohen BE, Smolderen K, Vittinghoff E, Whooley MA, Hiramoto J. Peripheral arterial disease, gender, and depression in the Heart and Soul Study. J Vasc Surg. 2014;60(2):396–403. pmid:24661811
  69. 69. Ragazzo L, Puech-Leao P, Wolosker N, de Luccia N, Saes G, Ritti-Dias RM, et al. Symptoms of anxiety and depression and their relationship with barriers to physical activity in patients with intermittent claudication. Clinics. 2021;76. pmid:33503171
  70. 70. Abi-Jaoudé JG, Naiem AA, Edwards T, Lukaszewski M-A, Obrand DI, Steinmetz OK, et al. Comorbid Depression is Associated with Increased Major Adverse Limb Events in Peripheral Arterial Disease: A systematic review and meta-analysis. Eur J Vasc Endovasc Surg. 2022. pmid:35483579
  71. 71. Ramirez JL, Grenon SM. Depression and peripheral artery disease: why we should care and what we can do. CVIR Endovasc. 2018;1(1):14. pmid:30652146
  72. 72. Pedersen SS, Denollet J, Spindler H, Ong AT, Serruys PW, Erdman RA, et al. Anxiety enhances the detrimental effect of depressive symptoms on health status following percutaneous coronary intervention. J Psychosom Res. 2006;61(6):783–9. pmid:17141666
  73. 73. Garcia-Diaz AM, Marchena PJ, Toril J, Arnedo G, Muñoz-Torrero JFS, Yeste M, et al. Alcohol consumption and outcome in stable outpatients with peripheral artery disease. J Vasc Surg. 2011;54(4):1081–7. pmid:21684714
  74. 74. Manfredini R, Lamberti N, Manfredini F, Straudi S, Fabbian F, Rodriguez Borrego MA, et al. Gender differences in outcomes following a pain-free, home-based exercise program for claudication. J Womens Health. 2019;28(9):1313–21. pmid:30222507
  75. 75. Agarwal S. The association of active and passive smoking with peripheral arterial disease: results from NHANES 1999–2004. Angiology. 2009;60(3):335–45. pmid:19153101
  76. 76. Willigendael EM, Teijink JA, Bartelink M-L, Kuiken BW, Boiten J, Moll FL, et al. Influence of smoking on incidence and prevalence of peripheral arterial disease. J Vasc Surg. 2004;40(6):1158–65. pmid:15622370
  77. 77. Gardner AW. The effect of cigarette smoking on exercise capacity in patients with intermittent claudication. Vasc Med. 1996;1(3):181–6. pmid:9546936
  78. 78. Fritschi C, Collins EG, O’Connell S, McBurney C, Butler J, Edwards L. The effects of smoking status on walking ability and health-related quality-of-life in patients with peripheral arterial disease. The Journal of cardiovascular nursing. 2013;28(4):380. pmid:22495802
  79. 79. Karatzi K, Papamichael C, Aznaouridis K, Karatzis E, Lekakis J, Matsouka C, et al. Constituents of red wine other than alcohol improve endothelial function in patients with coronary artery disease. Coron Artery Dis. 2004;15(8). pmid:15585989
  80. 80. Camargo CA, Stampfer MJ, Glynn RJ, Gaziano JM, Manson JE, Goldhaber SZ, et al. Prospective Study of Moderate Alcohol Consumption and Risk of Peripheral Arterial Disease in US Male Physicians. Circulation. 1997;95(3):577–80. pmid:9024142
  81. 81. Friedman AS. Smoking to cope: Addictive behavior as a response to mental distress. J Health Econ. 2020;72:102323. pmid:32505043
  82. 82. Breslau N, Peterson EL, Schultz LR, Chilcoat HD, Andreski P. Major depression and stages of smoking: A longitudinal investigation. Arch Gen Psychiatry. 1998;55(2):161–6.
  83. 83. Bolton JM, Robinson J, Sareen J. Self-medication of mood disorders with alcohol and drugs in the National Epidemiologic Survey on Alcohol and Related Conditions. J Affect Disord. 2009;115(3):367–75. pmid:19004504
  84. 84. Sullivan LE, Fiellin DA, O’Connor PG. The prevalence and impact of alcohol problems in major depression: a systematic review. The American journal of medicine. 2005;118(4):330–41. pmid:15808128
  85. 85. Regensteiner JG, Hiatt WR, Coll JR, Criqui MH, Treat-Jacobson D, McDermott MM, et al. The impact of peripheral arterial disease on health-related quality of life in the Peripheral Arterial Disease Awareness, Risk, and Treatment: New Resources for Survival (PARTNERS) Program. Vasc Med. 2008;13(1):15–24. pmid:18372434
  86. 86. Maksimovic M, Vlajinac H, Marinkovic J, Kocev N, Voskresenski T, Radak D. Health-related quality of life among patients with peripheral arterial disease. Angiology. 2014;65(6):501–6. pmid:23657177
  87. 87. Faller H, Störk S, Schuler M, Schowalter M, Steinbüchel T, Ertl G, et al. Depression and disease severity as predictors of health-related quality of life in patients with chronic heart failure—a structural equation modeling approach. J Card Fail. 2009;15(4):286–92.e2. pmid:19398075
  88. 88. Stewart KJ, Hiatt WR, Regensteiner JG, Hirsch AT. Exercise training for claudication. N Engl J Med. 2002;347(24):1941–51. pmid:12477945
  89. 89. Kruidenier LM, Viechtbauer W, Nicolai SP, Buller H, Prins MH, Teijink JA. Treatment for intermittent claudication and the effects on walking distance and quality of life. Vascular. 2012;20(1):20–35. pmid:22271802
  90. 90. Guidon M, McGee H. Exercise-based interventions and health-related quality of life in intermittent claudication: a 20-year (1989–2008) review. Eur J Cardiovasc Prev Rehabil. 2010;17(2):140–54. pmid:20215969
  91. 91. Chetter IC, Dolan P, Spark JI, Scott DJ, Kester RC. Correlating clinical indicators of lower-limb ischaemia with quality of life. Cardiovasc Surg. 1997;5(4):361–6. pmid:9350789
  92. 92. Barletta G, Perna S, Sabba C, Catalano A, O’Boyle C, Brevetti G. Quality of life in patients with intermittent claudication: relationship with laboratory exercise performance. Vasc Med. 1996;1(1):3–7. pmid:9546911
  93. 93. Long J, Modrall JG, Parker BJ, Swann A, Welborn MB 3rd, Anthony T. Correlation between ankle-brachial index, symptoms, and health-related quality of life in patients with peripheral vascular disease. J Vasc Surg. 2004;39(4):723–7. pmid:15071432
  94. 94. Pell JP. Impact of intermittent claudication on quality of life. The Scottish Vascular Audit Group. Eur J Vasc Endovasc Surg. 1995;9(4):469–72. pmid:7633995
  95. 95. Harwood AE, Totty JP, Broadbent E, Smith GE, Chetter IC. Quality of life in patients with intermittent claudication. Gefasschirurgie. 2017;22(3):159–64. pmid:28529410
  96. 96. Freitag MH, Bayerl B, Alber K, Gensichen J, Nagel E, Wohlgemuth WA. Gesundheitsbezogene Lebensqualität als Priorisierungskriterium in der Therapie der peripheren arteriellen Verschlusskrankheit. 2013.
  97. 97. Aboyans V, Ricco JB, Bartelink MEL, Bjorck M, Brodmann M, Cohnert T, et al. 2017 ESC Guidelines on the Diagnosis and Treatment of Peripheral Arterial Diseases, in collaboration with the European Society for Vascular Surgery (ESVS): Document covering atherosclerotic disease of extracranial carotid and vertebral, mesenteric, renal, upper and lower extremity arteriesEndorsed by: the European Stroke Organization (ESO)The Task Force for the Diagnosis and Treatment of Peripheral Arterial Diseases of the European Society of Cardiology (ESC) and of the European Society for Vascular Surgery (ESVS). Eur Heart J. 2018;39(9):763–816. pmid:28886620
  98. 98. Norgren L, Hiatt WR, Dormandy JA, Nehler MR, Harris KA, Fowkes FGR. Inter-society consensus for the management of peripheral arterial disease (TASC II). J Vasc Surg. 2007;45(1):S5–S67.
  99. 99. Kivimäki M, Steptoe A. Effects of stress on the development and progression of cardiovascular disease. Nature Reviews Cardiology. 2018;15(4):215. pmid:29213140
  100. 100. Huffman JC, Mastromauro CA, Beach SR, Celano CM, DuBois CM, Healy BC, et al. Collaborative Care for Depression and Anxiety Disorders in Patients With Recent Cardiac Events: The Management of Sadness and Anxiety in Cardiology (MOSAIC) Randomized Clinical Trial. JAMA Internal Medicine. 2014;174(6):927–35. pmid:24733277
  101. 101. Huffman JC, Mastromauro CA, Sowden G, Fricchione GL, Healy BC, Januzzi JL. Impact of a depression care management program for hospitalized cardiac patients. Circ Cardiovasc Qual Outcomes. 2011;4(2):198–205. pmid:21386067
  102. 102. Callahan CM, Kroenke K, Counsell SR, Hendrie HC, Perkins AJ, Katon W, et al. Treatment of depression improves physical functioning in older adults. J Am Geriatr Soc. 2005;53(3):367–73. pmid:15743276
  103. 103. Lichtman JH, Bigger JT Jr, Blumenthal JA, Frasure-Smith N, Kaufmann PG, Lespérance Fo, et al. Depression and coronary heart disease: recommendations for screening, referral, and treatment: a science advisory from the American Heart Association Prevention Committee of the Council on Cardiovascular Nursing, Council on Clinical Cardiology, Council on Epidemiology and Prevention, and Interdisciplinary Council on Quality of Care and Outcomes Research: endorsed by the American Psychiatric Association. Circulation. 2008;118(17):1768–75. pmid:18824640
  104. 104. Batty GD, Russ TC, Stamatakis E, Kivimäki M. Psychological distress and risk of peripheral vascular disease, abdominal aortic aneurysm, and heart failure: pooling of sixteen cohort studies. Atherosclerosis. 2014;236(2):385–8. pmid:25137648
  105. 105. Heikkilä K, Pentti J, Madsen IE, Lallukka T, Virtanen M, Alfredsson L, et al. Job strain as a risk factor for peripheral artery disease: a multi-cohort study. Journal of the American Heart Association. 2020;9(9):e013538. pmid:32342765
  106. 106. Berger JS, Ladapo JA. Underuse of Prevention and Lifestyle Counseling in Patients With Peripheral Artery Disease. J Am Coll Cardiol. 2017;69(18):2293–300. pmid:28473134
  107. 107. Schwarzer R. Modeling health behavior change: How to predict and modify the adoption and maintenance of health behaviors. Applied psychology. 2008;57(1):1–29.
  108. 108. Lightfoot K, Panagiotaki G, Nobes G. Effectiveness of psychological interventions for smoking cessation in adults with mental health problems: A systematic review. Br J Health Psychol. 2020;25(3):615–38. pmid:32678937
  109. 109. Lantz B. The large sample size fallacy. Scand J Caring Sci. 2013;27(2):487–92. pmid:22862286