Abstract
Background
Depression is one of the commonest neuropsychiatric disorders in patients with diabetes mellitus (DM) and is associated with poor glycaemic control, vascular complications, a low quality of life and increased health care expenditure. Co-morbid DM and depression remains poorly identified and inadequately treated in sub-Saharan Africa.
Methods
We conducted a cross-sectional survey of 437 patients with DM at 3 DM clinics in Uganda. Participants were assessed for depression, blood sugar levels, diabetic neuropathy, quality of life, and health care expenditures.
Results
The prevalence of depression was 34.8%. Depressed participants were more likely to be suicidal [OR=3.81, (CI 2.87–5.04)], younger [OR=3.98 CI (1.20–13.23)], un-employed [OR=1.99(CI 1.04–3.81)], and having lost a spouse [OR=2.36 (CI 1.29–4.31)]. Overall quality of life was poor [OR=0.67 (CI 0.47–0.96)], they scored poorer in the physical [OR=0.97, (CI 0.95–0.99)], psychological [OR=1.05 (CI 1.03–1.07)], and environmental [OR=0.97, (CI 0.95–0.99)] domains. They had an increased likelihood of incurring direct out-of-pocket payments for health care services [OR=1.56 (CI 1.03–2.36)], and were more likely to be impoverished [OR=1.52 (CI 1.01–2.28)].
Limitation
The cross sectional nature of this study makes it difficult to examine causation. More studies are required in order to better understand the associations and impact of the factors examined above on patient outcomes.
Conclusions
Depression is highly prevalent among patients with DM in Uganda, and is associated with a number of adverse outcomes. A holistic approach that focuses on the depression management among patients with diabetes is recommended.
1. Introduction and background
Diabetes mellitus (DM) a chronic and disabling disease, is a major contributor to disability adjusted life years (Murray et al., 2012; International Diabetes Federation, 2013). Approximately 6.7% of people worldwide suffer from DM, and this figure is anticipated to rise to 7.8% by 2030. The prevalence of DM is on the increase the world over. In a national survey conducted in Australia, between 2001 and 2008, there was a 36% increase in the prevalence of DM in persons older than 25 years (Atlantis, 2012). Moreover, it is predicted that by 2030, there will be a 69% rise in prevalence of DM in low and middle income countries (LMIC) compared to a 20% rise in high income countries (HIC) (Shaw et al., 2009). Recent evidence already shows a rise in the prevalence of DM in sub-Saharan Africa (SSA) (Abegunde et al., 2007; Mbanya et al., 2010; Peer et al., 2012). The prevalence of DM in Uganda was reported as 7.4% in a recent population survey (Mayega et al., 2013).
A number of studies that have examined the causative relationship between DM and depression have shown that DM patients are more likely to develop depressive disorder compared to members of the general population (Renn et al., 2011; Rustad et al., 2011; Katon 2011; Stuarta and Baune, 2012). For example, results from systematic reviews (Anderson et al., 2001; Nouwen et al., 2010) and a host of other studies (Renn et al., 2011; Rustad et al., 2011; Katon, 2011; Stuarta and Baune, 2012) have documented increased likelihood (up to 2 fold) of developing depression in DM patients compared to non-DM patients (Nouwen et al., 2010). Indeed a number of studies including meta-analyses by Ali et al. (2006) and Mendenhall et al. (2014) have documented high depression prevalence in DM patients (17.6 and 35.7%, respectively).
During the course of their illness, patients with co-morbid DM and depression suffer from a number of adverse health complications that negatively impact both DM and depression treatment outcomes. For example, existing literature (Lin et al., 2004; Ciechanowski et al., 2000) including a meta-analysis of 47 studies by Gonzalez et al. (2008b) show that patients with co-morbid DM and depression are almost two times less likely to adhere to hypoglycaemic medications compared to DM patients without depression. Literature also shows that patients with co-morbid DM and depression adhere poorly to dietary recommendations, exercise regimens and foot care (Gonzalez et al., 2008a). Moreover suboptimal adherence to both medications and dietary regimens has been associated with poor glycaemic control. Poor glycaemic control predicts vascular complications including stroke (deGroot et al., 2001; Katon et al., 2009; Lin et al., 2010; Sanal et al., 2011). Some work also shows that co-morbid DM and depression is associated with poor quality of life (Goldney et al., 2004; Lustman and Clouse, 2005; Egede and Hernández-Tejada, 2013). Poor quality of life may significantly impede patient recovery from existing ailments, as they often have a negative perception toward their lives.
Current evidence also shows that patients with co-morbid DM and depression have increased health care costs compared to members of the general public. In a review of 62 studies by Molosankwe et al. (2012), patients with co-morbid DM and depression were more likely to have an increased expenditure on their health care compared to non-depressed DM patients. Indeed, some studies have shown that patients with co-morbid DM and depression are likely to spend twice the amount of money on DM related medical costs, and four times on total medical costs compared to DM patients without co-morbid depression (Le et al., 2006; Egede and Ellis, 2010). Increased health care expenditures in patients with co-morbid DM and depression in SSA where direct out-of-pocket payment is the dominant health care financing mechanism could drive them into poverty.
The majority of studies that have investigated the burden of depression in DM and the adverse outcomes associated with it have been conducted in high income countries (HIC), with little work having been done in SSA. Moreover, generalizability of data about the burden of co-morbid DM and depression from HIC to SSA settings is limited in two important respects. First, the high patient–clinician ratio in SSA could have a direct impact on the ability of clinicians to identify and treat mental illnesses including depression (Kigozi et al., 2010; Faydi et al., 2011), leading to under-reporting of mental illnesses in DM patients. Second, cultural factors and explanatory models of diseases differ between SSA and HIC populations (Tylee, 1999; Okello and Ekblad, 2006), and so the ability of patients to report symptoms of mental illnesses, and disease presentation may be influenced by such factors. As recommended in a review by Lloyd et al. (2012), the understanding of mental illnesses, and cultural diversity issues need to be considered while assessing people for mental illness. Differences in cultural presentation and appreciation of mental illness, and high patient ratios between the two settings call for more studies to further examine the occurrence of co-morbid DM and depression.
In this study, we assessed the prevalence of depression and suicidality among patients with DM at three referral hospitals in Uganda. The factors that are associated with co-morbid DM and depression including fasting blood sugar levels, diabetic neuropathy, quality of life, and health care expenditure (direct out-of-pocket payment and its impact) were also assessed.
2. Methods
2.1. Study design and setting
This was a cross sectional study at the out-patients DM clinics of Mulago, Mbarara and Gulu hospitals in Uganda. Mulago Hospital is a national referral 1500 bed capacity Hospital in the centre of Kampala, the capital city of Uganda. Mbarara Hospital is a 600 bed capacity regional referral hospital 275 km west of the capital Kampala. Gulu regional referral Hospital is 340 km north of the capital Kampala. All three hospitals have diabetic clinics which run once a week with an average of 100 patients seen daily (150 Mulago, 100 Mbarara and 50 in Gulu).
2.2. Study procedure
Participants were enrolled if they were confirmed DM patients attending the DM clinic, 18 years and older and able to provide informed consent. All participants provided written informed consent before being enrolled into the study. To prevent making a diagnosis of acute psychological distress or adjustment reaction resulting from recently receiving a diagnosis of DM, participants were only included if they had been diagnosed as diabetic, and attended the DM clinic for at least 2 months.
We used a simple random sampling technique to select patients from clinic attendees till the total sample of 437 was accrued. Trained medical officers obtained consent from the eligible participants before administering the study questionnaires and conducting a diagnostic depressive disorder interview. Data was collected over a 6 month period between November 2013 and April 2014.
Approval for the study was obtained from all relevant authorities including the Makerere University College of Health Sciences ethical committee (#REC REF 2013-135) and the Uganda National Council of Science and Technology (SS 3389). All participants provided written informed consent before being enrolled into the study.
2.3. Measures
The following data was collected from all 437 participants: (a) sociodemographic information including marital status, age, education level and occupation, (b) depression diagnosis and suicidality using the mini international neuropsychiatric inventory (MINI) (Sheehan et al., 1998), (c) diabetic neuropathy using the Michigan Neuropathic Screening Instrument (MNSI) (Feldman et al., 1994), (d) quality of life using the World Health Organization brief quality of life scale (WHO-QOL) (The World Health Organization quality of life assessment (WHOQOL), 1995), (e) health care expenditure and house socio-economic status (SES) based on reported household income from employment, household enterprises, current transfers and other benefits, property income and any other income sources using a standardized questionnaire.
2.4. Data analysis plan
Data was analyzed using STATA 11.2(STATA Statistics/Data Analysis 4905 Lakeway Drive College Station Texas 77845 USA 800-STATA-PC http://www.stata.com) (STATA, 2011). The presence of depression was the dependent variable; suicadility, socioeconomic variables, fasting blood sugar levels, diabetic neuropathy, quality of life, and health care expenditure (direct out-of-pocket payments and impoverishment due to these direct out-of-pocket payments) were the independent variables. Factors found statistically significant at bi-variable analysis (p-value ≤ 0.05) were entered into a stepwise logistic regression model to test for associations, controlling for age and gender.
For the analysis of association between the presence of depression and impoverishment due to direct out-of-pocket payments incurred by the DM patients, the study adjusts the Foster–Greer–Thorbecke (FGT) indices for poverty measurement for the impact of direct out-of-pocket payments using the approach by Wagstaff and Doorslaer (2003). Using this approach, variables that capture households who are pushed below the $1.25/day poverty line and those whose depth of poverty increases due to direct out-of-pocket payments for DM were generated.
2.5. Results
The prevalence of depression was 34.8%. Of the 437 participants enrolled, 54.4% (238) were from Mulago Hospital, 22.7% (99) from Mbarara Hospital and 22.9% (100) from Gulu Hospital. About 2/3rd 64.8% (283) of the participants were females. The mean age of the participants was 51 years (SD14.06, Range 18–90). The mean random blood sugar was 9.75 (SD6.86 Range 5.1–19.6) and 69.5% (303) of the participants had diabetic neuropathy.
At multivariable analysis, there was no statistically significant difference between the depressed and non-depressed participants by gender, blood sugar level, and presence of diabetic neuropathy. After controlling for age and gender, depressed patients were more likely to be suicidal [OR=3.81, (CI 2.87–5.04)], younger [OR=3.98 CI (1.20–13.23)], un-employed [OR=1.99(CI 1.04–3.81)], and lost a spouse [OR=2.36 (CI 1.29–4.31)]. Table 1. Depressed participants perceived their overall quality of life as poor [OR=0.67 (CI 0.47–0.96)], and scored poorer on the physical [OR=0.97, (CI 0.95–0.99)], psychological [OR=1.05 (CI 1.03–1.07)], and environmental [OR=0.97, (CI 0.95–0.99)] QOL domains (Table 2).
Table 1.
Variables | Unadjusted OR (95% CI) | p-Value | Adjusted OR (95% CI) | p-Value |
---|---|---|---|---|
Blood sugar level (mmol/l) | ||||
<3.9 | ||||
3.9–7.2 | 0.94 (0.23–3.85) | 0.936 | 0.90 (0.21–3.87) | 0.889 |
>7.2 | 1.37 (0.35–5.43) | 0.652 | 1.34 (0.32–5.58) | 0.691 |
Age | ||||
18–30 | ||||
31–43 | 3.18 (1.08–9.37) | 0.035 | 3.98 (1.20–13.23) | 0.024 |
44–56 | 2.71 (0.99–7.45) | 0.053 | 2.82 (0.91–8.69) | 0.071 |
57–69 | 4.36 (1.57–12.13) | 0.005 | 3.66 (1.17–11.44) | 0.389 |
≥70 | 2.50 (0.80–7.83) | 0.117 | 1.77 (0.48–6.51) | 0.389 |
Gender | ||||
Male | ||||
Female | 1.38 (1.01–2.48) | 0.043 | 1.01 (0.60–1.70) | 0.061 |
Marital status | ||||
Married | ||||
Never married | 1.15 (0.53–2.51) | 0.718 | 1.80 (0.72–4.46) | 0.206 |
Widowed/widower | 2.57 (0.52–4.35) | <0.001 | 2.36 (1.29–4.31) | 0.005 |
Separated/divorced | 1.34 (0.66–2.71) | 0.423 | 1.40 (0.66–2.97) | 0.384 |
Occupation | ||||
Employed | ||||
Peasant farmer | 2.16 (1.25–3.73) | 0.006 | 1.81 (1.01–3.26) | 0.048 |
Unemployed | 1.99 (1.10–3.59) | 0.023 | 1.99 (1.04–3.81) | 0.037 |
Other | 1.64 (0.78–3.45) | 0.191 | 1.29 (0.59–2.86) | 0.523 |
Suicidality | 3.71 (2.84–4.83) | <0.001 | 3.81 (2.87–5.05) | <0.001 |
Diabetic neuropathy | ||||
No | ||||
Yes | 1.73 (1.12–2.67) | 0.013 | 1.56 (0.98–2.47) | 0.061 |
Health care expenditure indices | ||||
Payment for health care services | 1.88 (1.10–2.56) | 0.026 | 1.56 (1.03–2.36) | 0.032 |
Being impoverished | 1.79 (1.44–3.00) | 0.033 | 1.52 (1.01–2.28) | 0.042 |
Table 2.
Domains | Median (IQR) | Unadjusted OR (95% CI) | p-Value | Adjusted OR (95% CI) | p-Value |
---|---|---|---|---|---|
Overall perception of QOL | 2 (2, 4) | 0.44 (0.34–0.56) | <0.001 | 0.67 (0.47–0.96 | 0.026 |
Overall perception of health | 3 (2, 4) | 0.26 (0.20–0.34) | <0.001 | 0.75 (0.53–1.07) | 0.110 |
Physical | 88 (76, 100) | 0.95 (0.93–0.96) | <0.001 | 0.97 (0.95–0.99) | 0.002 |
Social | 24 (20, 28) | 0.95 (0.92–0.97) | <0.001 | 0.99 (0.96–1.03) | 0.650 |
Psychological | 76 (69, 88) | 0.98 (0.97–0.99) | 0.002 | 1.05 (1.03–1.07) | <0.001 |
Environment | 100 (84, 116) | 0.96 (0.95–0.97) | <0.001 | 0.97 (0.95–0.99) | <0.001 |
Participants with co-morbid DM and depression were also more likely to incur direct out-of-pocket payments [OR=1.56 (CI 1.03–2.36)], and be impoverished [OR=1.52 (CI 1.01–2.28)] due to these payments.
3. Discussion
In this study we found a high (34.5%) prevalence of depression in DM patients, in keeping with rates reported in some studies conducted in SSA (Akinlade et al., 1996; Kagee 2008; Shehatah et al., 2010a, 2010b). A recent systematic review showed a wide variation in the prevalence of depression among DM patients in SSA (15.2–45.9%) (Mendenhall et al., 2014). The variations in the prevalence of depression among DM patients could be a result of a number of differences including different instruments (Akinlade et al., 1996; Ashraf, 2008; Shehatah et al., 2010a, 2010b) used to confirm the presence of depression, each with different cut-off scores for caseness. Studies assessing the prevalence of depression in persons with DM have been conducted in different settings including out-patients (Kagee, 2008), population surveys (Asghar et al., 2007), and the elderly (Shehatah et al., 2010a, 2010b). The use of depression screening instruments may fail to distinguish some conditions which mimic depressive disorders including depressive temperament. In a recent review by Gois et al. (2012), depressive temperament which presents with signs and symptoms of a depressive disorder (sadness, guilt, self-blame, being hypercritical of failures) is a common comobidity in persons with DM, and failure to distinguish these concepts may artificially inflate the prevalence of depression in the study population. These factors may account for differences in the prevalence of depression among DM patients.
Findings from the sociodemographic variables indicate that depression was associated with a younger age, loss of a spouse and lack of employment. While some studies have shown that patients with DM in the younger age group are more likely to suffer from co-morbid depression (Zhao et al., 2006; Wexler et al., 2012), others have found that association for older individuals (Khuwaja et al., 2010; Ganasegeran et al., 2014). One possible explanation could be that the younger individuals in our study population were not fully psychologically adjusted to having a chronic illness in the form of DM, and failed to cope with the numerous stressors that could have led them to develop of depression.
Previous studies have documented a positive association between lack of employment and co-morbid depression in persons with DM (Friis and Nanjundappa, 1986; Igwe et al., 2013). A number of explanations could be responsible for these findings. For example, the stress that results from people losing their job and source of livelihood could have led to the development of depression. However, the presence of a depressive illness could also be the cause of loss of employment, as individuals are no longer able to concentrate on their work, and labour under the illness.
The loss of a spouse has been documented as a predictor of depression in DM patients (Téllez-Zenteno and Cardiel, 2002; Hailemariam et al., 2012). Our findings are in keeping with these previous studies, and could be explained by the fact that loss of a spouse is associated with high levels of stress and could be aetiological in the development of depression.
We found no association between depression and the levels of blood sugar level in our study population. Previous work that has assessed for the association between depression and glycemic control in DM patients have produced mixed results. While some studies have documented positive associations between depression and glycemic control in DM patients (Lustman et al., 2000; Richardson et al., 2008), others have found no such associations (Fisher et al., 2010; Papelbaum et al., 2010). One possible explanation for our findings could be the fact that extensive adherence support is provided by diabetic nurses to patients attending these clinics, which improves patient’s ability to follow treatment regimens. Since poor glycaemic control has been associated with vascular complications including diabetic neuropathy (deGroot et al., 2001; Katon et al., 2009; Lin et al., 2010; Sanal et al., 2011), the fact that we found no association between poor glycemic control and depression could also explain the lack of association between diabetic neuropathy and depression observed in this study.
Our study found a positive association between depression and a poor quality of life in four out of the six domains of the WHO-QOL, including the overall perception of a poor quality of life, physical, psychological and environmental domains. Previous studies have documented such associations (Goldney et al., 2004; Kiadaliri et al., 2013; Egede and Hernández-Tejada, 2013). These findings could be a result of a number of factors. First, some depressive symptoms including loss of interests and feeling worthless can have a negative influence on one’s perception of life. The cross sectional nature of the study means that an alternative explanation for these findings could exist, since persons who were leading a poor quality of life may have become more prone to developing depression, due to their poor outlook of life events. Clinical complications such as diabetic neuropathies, which are common among DM patients, could also influence the perception of overall quality of life as poor by the participants. We found no association between being depressed and the social domain of the quality of life measure. This finding could be explained by the presence of support structures available in the communities from where these participants came.
Study findings showed that depressed participants were more likely to incur direct out-of-pocket payments and also get impoverished as a result of making these payments compared to DM patients without depression. Our findings are in congruence with others which have documented poor health economic indices in persons with co-morbid DM and depression including increase in health care expenditures (Le et al., 2006; Egede and Ellis, 2010). A possible explanation to these findings is the fact that depressed participants could have been making payments for the treatment of depressive disorder symptoms which the patients with DM do not make. At the 3 clinics where our data was collected, there were no mental health care services (identification and treatment of depressed patients), and so the majority of depressed patients are unlikely to have received treatment, let alone being aware of their illness. Such situations may force patients to self-medicate, increasing their health care expenditures which are detrimental to the welfare of the households.
3.1. Limitations
The cross sectional nature of this study makes it difficult to examine causation. More studies are required in order to better understand the associations and impact of the factors examined above on patient outcomes. Similarly, assessment of the poverty impact of direct out-of-pocket health payments needs complex household surveys.
3.2. Conclusions
Depression is highly prevalent among patients with DM in Uganda. The presence of co-morbid DM and depression is associated with a number of adverse outcomes like increased health expenditure and poorer quality of life. A holistic approach that focuses on the identification and management of depression among patients with diabetes is recommended.
Acknowledgments
Role of funding source
The project was supported by the MESAU-MEPI Programmatic Award through Award Number 1R24TW008886 from the Fogarty International Center.
Footnotes
Conflict of interest
The authors declare no conflict of interest.
Author consent forms
All the stated authors in this article consented to have their names in the article.
Dr Dickens Akena conceptualized the project. Dr’s Dickens Akena, Ekwaro Obuku, Phillipa Kadama, Rejani Lalitha, Dr Carolyne Akello and Mr Brendan Kwesiga wrote the protocol for the application of funds to conduct the study.
Dr Carolyne Akello was the statistician. Mr Brendan Kwesiga conducted the analysis of the health economics part of the project.
Dr’s Scholastic Ashaba, and James Okello supervised data collection at Mbarara and Gulu University, respectively. Dr Emmanuel Mwesiga supervised data collection at Mulago Hospital.
All the authors provided constructive comments in shaping the article.
The content is solely the responsibility of the authors and does not necessarily represent the official views of the Fogarty International Center or the National Institutes of Health.
References
- Akinlade KS, Ohaeri JU, et al. The psychological condition of a cohort of Nigerian diabetic subjects. Afr J Med Med Sci. 1996;25 (1):61–67. [PubMed] [Google Scholar]
- Ali S, Stone MA, et al. The prevalence of co-morbid depression in adults with Type 2 diabetes: a systematic review and meta-analysis. Diabet Med. 2006;23 (11):1165–1173. doi: 10.1111/j.1464-5491.2006.01943.x. [DOI] [PubMed] [Google Scholar]
- Asghar S, Hussain A, et al. Prevalence of depression and diabetes: a population-based study from rural Bangladesh. Diabet Med. 2007;24 (8):872–877. doi: 10.1111/j.1464-5491.2007.02136.x. [DOI] [PubMed] [Google Scholar]
- Atlantis E. Excess burden of type 1 and type 2 diabetes due to psychopathology. J Affect Disord Suppl. 2012:S136–141. 142. doi: 10.1016/S0165-0327(12)70007-1. doi:110.1016/S0165-0327(1012)70007-70001. [DOI] [PubMed] [Google Scholar]
- Abegunde Dele O, Mathers Colin D, et al. The burden and costs of chronic diseases in low-income and middle-income countries. Lancet. 2007;8(370) 9603:1929–1938. doi: 10.1016/S0140-6736(07)61696-1. [DOI] [PubMed] [Google Scholar]
- Ashraf Kagee. Symptoms of depression and anxiety among a sample of south african patients living with a chronic illness. S Afr J Health Psychol. 2008;13:547–555. doi: 10.1177/1359105308088527. [DOI] [PubMed] [Google Scholar]
- Anderson Ryan J, Freedland Kenneth E, et al. The prevalence of comorbid depression in adults with diabetes: a meta-analysis. Diabetes Care. 2001;24 (6):1069–1078. doi: 10.2337/diacare.24.6.1069. [DOI] [PubMed] [Google Scholar]
- Ciechanowski PS, Katon WJ, et al. Depression and diabetes: impact of depressive symptoms on adherence, function, and costs. Arch Intern Med. 2000;160 (21):3278–3285. doi: 10.1001/archinte.160.21.3278. [DOI] [PubMed] [Google Scholar]
- Egede Leonard E, Hernández-Tejada Melba A. Effect of comorbid depression on quality of life in adults with Type 2 diabetes. Review Informa Health Care. 2013;13 (1):83–91. doi: 10.1586/erp.12.86. http://dx.doi.org/10.1586/erp.1512.1586. [DOI] [PubMed] [Google Scholar]
- Egede Leonard E, Ellis Charles. Diabetes and depression: global perspectives. Diabetes Atlas. 2010;87:302–312. doi: 10.1016/j.diabres.2010.01.024. [DOI] [PubMed] [Google Scholar]
- Faydi Edwige, Funk Michelle, et al. An assessment of mental health policy in Ghana, South Africa, Uganda and Zambia. Health Res Policy Syst. 2011;9(17) doi: 10.1186/1478-4505-9-17. (Biomed central) [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feldman EL, Stevens MJ, et al. A practical two-step quantitative clinical and electrophysiological assessment for the diagnosis and staging of diabetic neuropathy. Diabetes Care. 1994;17:1281–1289. doi: 10.2337/diacare.17.11.1281. [DOI] [PubMed] [Google Scholar]
- Friis R, Nanjundappa G. Diabetes, depression and employment status. Soc Sci Med. 1986;23:471–475. doi: 10.1016/0277-9536(86)90006-7. [DOI] [PubMed] [Google Scholar]
- Fisher Lawrence, Glasgow Russell E, et al. The relationship between diabetes distress and clinical depression with glycemic control among patients with type 2 diabetes. Diabetes Care. 2010;33:1034–1036. doi: 10.2337/dc09-2175. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gois Carlos, Akiskal Hagop, et al. The relationship between temperament, diabetes and depression. J Affect Disord Suppl. 2012:S67–71. 142. doi: 10.1016/S0165-0327(12)70010-1. http://dx.doi.org/10.1016/S0165-0327(1012)70010-70011. [DOI] [PubMed]
- Gonzalez JS, Safren SA, et al. Symptoms of depression prospectively predict poorer self-care in patients with type 2 diabetes (2008 September) Diabet Med. 2008a;25 (9):1102–1107. doi: 10.1111/j.1464-5491.2008.02535.x. doi:1110.1111/j.1464-5491.2008.02535.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gonzalez Jeffrey S, Peyrot Mark, et al. Depression and diabetes treatment nonadherence: a meta-analysis. Diabetes Care. 2008b;31 (21):2398–2403. doi: 10.2337/dc08-1341. 2310.2337/dc2308-1341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ganasegeran Kurubaran, Renganathan Pukunan, et al. Factors associated with anxiety and depression among type 2 diabetes outpatients in Malaysia: a descriptive cross-sectional single-centre study. BMJ Open. 2014;4:e004794. doi: 10.1136/bmjopen-2014-004794. 004710.001136/bmjopen-002014–004794. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goldney Robert D, Phillips Pat J, et al. Diabetes, depression, and quality of life. A population study. Diabetes Care. 2004;27 (5):1066–1070. doi: 10.2337/diacare.27.5.1066. doi:1010.2337/diacare.1027.1065.1066. [DOI] [PubMed] [Google Scholar]
- Hailemariam Solomon, Tessema Fasil, et al. The prevalence of depression and associated factors in Ethiopia: findings from the National Health Survey. Int J Ment Health Syst. 2012;6:23. doi: 10.1186/1752-4458-6-23. http://dx.doi.org/10.1186/1752-4458-1186-1123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Igwe MN, Uwakwe R, et al. Factors associated with depression and suicide among patients with diabetes mellitus and essential hypertension in a Nigerian teaching hospital. Afr Health Sci. 2013;13 (1):68–77. doi: 10.4314/ahs.v13i1.10. http://dx.doi.org/10.4314/ahs.v4313i4311.4310. [DOI] [PMC free article] [PubMed] [Google Scholar]
- International Diabetes Federation. IDF Diabetes Atlas. 6. International Diabetes Federation; Brussels, Belgium: 2013. < http://www.idf.org/diabetesatlas>. [Google Scholar]
- Khuwaja Ali Khan, Lalani Saima, et al. Anxiety and depression among outpatients with type 2 diabetes: a multi-centre study of prevalence and associated factors. Diabetol Metab Syndr. 2010;2:72. doi: 10.1186/1758-5996-2-72. http://dx.doi.org/10.1186/1758-5996-1182-1172. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kiadaliri Aliasghar A, Najafi Baharak, et al. Quality of life in people with diabetes: a systematic review of studies in Iran. J Diabetes Metab Disord. 2013;12:54. doi: 10.1186/2251-6581-12-54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kagee Ashraf. Symptoms of depression and anxiety among a sample of South African patients living with a chronic illness. J Health Psychol. 2008;13 (4):547–555. doi: 10.1177/1359105308088527. doi:510.1177/1359105308088527. [DOI] [PubMed] [Google Scholar]
- Kigozi Fred, Ssebunnya Joshua, et al. An overview of Uganda’s mental health care system: results from an assessment using the world health organization’s assessment instrument for mental health systems (WHOAIMS) Int J Ment Health Syst. 2010;4:1. doi: 10.1186/1752-4458-4-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Katon Wayne J. Epidemiology and treatment of depression in patients with chronic medical illness. Dialogues Clin Neurosci. 2011;13:7–23. doi: 10.31887/DCNS.2011.13.1/wkaton. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Katon Wayne, Russo Joan, et al. Depression and diabetes: factors associated with major depression at 5-year follow-up. Psychosomatics. 2009;50 (6):570–579. doi: 10.1176/appi.psy.50.6.570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lloyd Cathy E, Roy Tapash, et al. Epidemiology of depression in diabetes: international and cross-cultural issues. J Affect Disord Suppl. 2012:S122–149. 142. doi: 10.1016/S0165-0327(12)70005-8. doi:110.1016/S0165-0327(1012)70005-70008. [DOI] [PubMed] [Google Scholar]
- Lin Elizabeth HB, Rutter Carolyn M, et al. Depression and advanced complications of diabetes: a prospective cohort study. Diabetes Care. 2010;33 (2):264–269. doi: 10.2337/dc09-1068. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lin Elizabeth HB, Katon Wayne, et al. Relationship of depression and diabetes self-care, medication adherence, and preventive care. Diabetes Care. 2004;27(9):2154–2160. doi: 10.2337/diacare.27.9.2154. [DOI] [PubMed] [Google Scholar]
- Lustman Patrick J, Clouse Ray E. Depression in diabetic patients the relationship between mood and glycemic control. J Diabet Complications. 2005;19:113–122. doi: 10.1016/j.jdiacomp.2004.01.002. [DOI] [PubMed] [Google Scholar]
- Lustman Patrick J, Anderson Ryan J, et al. Depression and poor glycemic control: a meta-analytic review of the literature. Diabetes Care. 2000;23 (7):934–942. doi: 10.2337/diacare.23.7.934. [DOI] [PubMed] [Google Scholar]
- Le Trong K, Able Stephen L, et al. Resource use among patients with diabetes, diabetic neuropathy, or diabetes with depression. BMC Cost Effectiveness Resour Allocation. 2006;4 (18):23. doi: 10.1186/1478-7547-4-18. http://dx.doi.org/10.1186/1478-7547-1184-1118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murray Christopher JL, Vos Theo, et al. Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012;380:2197–2223. doi: 10.1016/S0140-6736(12)61689-4. [DOI] [PubMed] [Google Scholar]
- Mendenhall Emily, Norris Shane A, et al. Depression and type 2 diabetes in low- and middleincome countries: a systematic review. Diabetes Res Clin Pract. 2014;103 (2):276–285. doi: 10.1016/j.diabres.2014.01.001. doi:210.1016/j.diabres.2014.1001.1001. Epub 2014 Jan 1013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mendenhall Emily, Norris Shane A, et al. Depression and type 2 diabetes in low- and middleincome countries: a systematic review. Diabetes Res Clin Pract. 2014 doi: 10.1016/j.diabres.2014.01.001. http://dx.doi.org/10.1016/j.diabres.2014.1001.1001. [DOI] [PMC free article] [PubMed]
- Molosankwe Iris, Patel Anita, et al. Economic aspects of the association between diabetes and depression: a systematic review. J Affect Disord. 2012;142S141:S142–S155. doi: 10.1016/S0165-0327(12)70008-3. [DOI] [PubMed] [Google Scholar]
- Mbanya Jean Claude N, Motala Ayesha A, et al. Diabetes in sub-Saharan Africa. Lancet. 2010;375:2254–2266. doi: 10.1016/S0140-6736(10)60550-8. [DOI] [PubMed] [Google Scholar]
- Mayega Roy William, Guwatudde David, et al. Diabetes and pre-diabetes among persons aged 35 to 60 years in Eastern Uganda: prevalence and associated factors. PLoS One. 2013;8 (8):e72554. doi: 10.1371/journal.pone.0072554. 72510.71371/journal.pone.0072554. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nouwen A, Winkley K, et al. Type 2 diabetes mellitus as a risk factor for the onset of depression: a systematic review and meta-analysis. Diabetologia. 2010;53:2480–2486. doi: 10.1007/s00125-010-1874-x. doi:2410.1007/s00125-00010-01874-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Okello ES, Ekblad S. Lay concepts of depression among the Baganda of Uganda. a pilot study. Transcult Psychiatry. 2006;43:287–313. doi: 10.1177/1363461506064871. [DOI] [PubMed] [Google Scholar]
- Papelbaum M, Lemos HM, et al. The association between quality 0of life, depressive symptoms and glycemic control in a group of type 2 diabetes patients. Diabetes Res Clin Pract. 2010;89:227–230. doi: 10.1016/j.diabres.2010.05.024. [DOI] [PubMed] [Google Scholar]
- Peer Nasheeta, Steyn Krisela, et al. Rising diabetes prevalence among urban-dwelling Black South Africans. PLoS One. 2012;7 (9):e43336. doi: 10.1371/journal.pone.0043336. doi:43310.41371/journal.pone.0043336. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Renn Brenna N, Feliciano Leilani, et al. The bidirectional relationship of depression and diabetes: a systematic review. Clin Psychol Rev. 2011;31:1239–1246. doi: 10.1016/j.cpr.2011.08.001. [DOI] [PubMed] [Google Scholar]
- Rustad James K, Musselman Dominique L, et al. The relationship of depression and diabetes: pathophysiological and treatment implications. Psychoneuroendocrinology. 2011;36:1276–1286. doi: 10.1016/j.psyneuen.2011.03.005. [DOI] [PubMed] [Google Scholar]
- Richardson Lisa K, Egede Leonard E, et al. Longitudinal effects of depression on glycemic control in veterans with type 2 diabetes. Gen Hosp Psychistry. 2008;30 (6):509–514. doi: 10.1016/j.genhosppsych.2008.07.001. doi:510.1016/j.genhosppsych.2008.1007.1001. Epub 2008 Sep 1011. [DOI] [PubMed] [Google Scholar]
- Shehatah Ashraf, Rabie Menan A, et al. Prevalence and correlates of depressive disorders in elderly with type 2 diabetes in primary health care settings. J Affect Disord. 2010a;123 (1–3):197–201. doi: 10.1016/j.jad.2009.09.002. doi:110.1016/j.jad.2009.1009.1002. Epub 2009 Oct 1014. [DOI] [PubMed] [Google Scholar]
- Shaw JE, Sicree RA, et al. Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res Clin Pract. 2009;87:4–14. doi: 10.1016/j.diabres.2009.10.007. http://dx.doi.org/10.1016/j.diabres.2009.1010.1007 (Epub 2009 Nov 1016) [DOI] [PubMed] [Google Scholar]
- Stuarta Michael J, Baune Bernhard T. Depression and type 2 diabetes: inflammatory mechanisms of a psychoneuroendocrine co-morbidity. Neurosci Biobehav Rev. 2012;36:658–676. doi: 10.1016/j.neubiorev.2011.10.001. [DOI] [PubMed] [Google Scholar]
- Sheehan DV, Lecrubier Y, et al. The mini international neuropsychiatric interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview. J Clin Psychiatry. 1998;59:22–23. [PubMed] [Google Scholar]
- Shehatah A, Rabie M, et al. Prevalence and correlates of depressive disorders in elderly with type 2 diabetes in primary health care settings. J Affect Disord. 2010b;123 (1–3):197–201. doi: 10.1016/j.jad.2009.09.002. [DOI] [PubMed] [Google Scholar]
- STATA. Statistics/Data Analysis 4905 Lakeway Drive College Station Texas 77845 USA 800-STATA-PC. STATA; 2011. < http://www.stata.com>. [Google Scholar]
- Sanal TS, Nair NS, et al. Factors associated with poor control of type 2 diabetes mellitus: a systematic review and meta-analysis. J Diabetol. 2011 Oct;2011:3. [Google Scholar]
- Téllez-Zenteno José Francisco, Cardiel Mario H. Risk factors associated with depression in patients with type 2 diabetes mellitus. Arch Med Res. 2002;33 (1):53–60. doi: 10.1016/s0188-4409(01)00349-6. [DOI] [PubMed] [Google Scholar]
- The World Health Organization quality of life assessment (WHOQOL) Position paper from the World Health Organization. Soc Sci Med. 1995;41 (10):1403–1409. doi: 10.1016/0277-9536(95)00112-k. [DOI] [PubMed] [Google Scholar]
- Tylee A. Depression in the community: physician and patient perspective. J Clin Psychiatry. 1999;60 (Suppl 7):12–16. [PubMed] [Google Scholar]
- Wexler Deborah J, Porneala Bianca, et al. Diabetes differentially affects depression and self-rated health by age in the U.S. Diabetes Care. 2012;35:1575–1577. doi: 10.2337/dc11-2266. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wagstaff A, Doorslaer E. Catastrophe and impoverishment in paying for health care: with applications to Vietnam 1993–1998. Health Econ. 2003;12 (11):921–933. doi: 10.1002/hec.776. [DOI] [PubMed] [Google Scholar]
- Zhao W, Chen Y, et al. Association between diabetes and depression: sex and age differences. Public Health. 2006;120 (8):696–704. doi: 10.1016/j.puhe.2006.04.012. Epub 2006 Jul 2007. [DOI] [PubMed] [Google Scholar]
- deGroot Mary, Anderson Ryan, et al. Association of depression and diabetes complications: a meta-analysis. Psychosom Med. 2001;63:619–630. doi: 10.1097/00006842-200107000-00015. [DOI] [PubMed] [Google Scholar]