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Psychosocial and clinical factors associated with depression among individuals with diabetes in Bahir Dar City Administrative, Northwest Ethiopia

Abstract

Background

In a context of the potential epidemic nature of both diabetes mellitus (DM) and depression had negative effects in cases of disability and mortality. Coexisting depression had been linked to morbidity and mortality in people with diabetes. Therefore, this study aimed to identify psychosocial and clinical factors associated to develop depression symptoms in diabetes patients.

Methods

A systematic institution based cross-sectional study design was conducted from 1st March to 8th April 2016 among adult diabetes patent. Depression status was assessed by the Patient Health Questionnaire-9 (PHQ-9). Data were analyzed by logistic regression and at P < 0.05 with 95% CI was considered statistically significant.

Result

A total of 416 patients were included in this studied. Based on PHQ-9, self- reported depression symptom was 29.3% [95% CI 25.2, 33.4]. In the performed statistical evaluation, patients whose age was between 45 and 54 years old (AOR = 3.88; 95% CI 1.36, 11.08); being female (AOR = 2.43; 95% CI 1.29, 4.58); who has poor social support (AOR = 6.08; 95% CI 2.98, 12.40); and who has high fear of kidney problems secondary to DM (AOR = 6.12; 95% CI 1.75, 21.23) were statistically associated with depressive symptoms in diabetes patients.

Conclusion

This study demonstrated that complication fears, social support, being female and sexual dysfunction were found significantly associated with co-morbid depression in diabetes. Therefore, availed a social network of family and friends; providing diabetes education to address the patient’s fear of complications; and considered a sexual function is an integral part of overall health in diabetic patients.

Background

Diabetes mellitus (DM) is a chronic metabolic disorder. It affects the productive age group. Globally, an estimated 422 million. adults were living with diabetes in 2014. By 2030 this will have risen to 552 million. people. DM was a cause of 4.6 million. deaths in 2011 [1, 2]. Studies showed that diabetes and depression occur together approximately twice as frequently as would be predicted by chance alone [3]. Depression is a common mental disorder characterized by sadness, loss of interest or pleasure, feelings of guilt or low self-worth, disturbed sleep or appetite, feelings of tiredness, and poor concentration [4]. Currently, at a global level, over 350 million. people are suffering from depression and its leading cause of disability [5].

It is believed that the relationship of diabetes to depression is bidirectional. That is why depression can lead to diabetes and conversely, diabetes could facilitate the emergence of depression [6]. Diabetes mellitus can cause psychological, emotional, social and psychosexual problems. Depression is also a risk factor as well as complications of diabetes [5, 6]. Individuals with diabetes have a 2- to 3-fold increased risk for depression. Depression affecting approximately one in every five diabetes patients compared to the general population [5, 7]. Co-morbid diabetes and depression are a major clinical challenge as a treatment outcome of both conditions are worsened by one the other [3].

Previous studies documented that socio-demographic, clinical and psychosocial factors contributing to the development of co-morbid depression among diabetes patients. Socio-demographic factors that were significantly associated with depression in people with diabetes were; older age, lower socioeconomic status, monthly household income and ethnicity [8,9,10], level of education [12], female gender [13] and being single [14]. A clinical factors which were linked to depression in diabetic patients were presence of complication [12], co-morbidities, duration of treatment and treatment with insulin [10], duration of illness more than 10 years [15], limb problems [16], presence of ≥ 3 diabetic complications, and negative life events and poor social support [17], total number of life events were statistically significant predictors of depression in diabetes patient [18].

Behavioral related factors that were significantly influenced co-morbid depression in diabetes patients were also: social inhibition and negatively affective life [19], poor social support [14, 20], physical quality of life [21], future diet behavior, physical activity and glucose testing [22]. A literature review reported that diabetes individuals who suffer from depression, DM related complications, and lack of social support were worse general health [23].

Psychosocial and clinical factors on co-morbid depression influence living with diabetes, both type 1 and type 2 [24]. Although the above factors were associated with depression, most of these studies were based on in developed countries, with only some exceptions. Therefore, these findings cannot be generalized to Ethiopia, especially in the study area. Thus, our study aimed to identify psychosocial and clinical factors associated with co-morbid depression among diabetes patients treated at the Felege Hiwot Referral Hospital (FHRH), Bahir Dar, Northwest Ethiopia.

Methods

Study setting and population

A facility-based cross-sectional study was conducted from 1st March to 8th April 2016 at FHRH. FHRH is found in Bahir Dar city administration, Northwest Ethiopia. The hospital was opened for 24 h for emergency service. It provides promotive, preventive, curative and rehabilitative services.

The service was rendered by the physician and nurses. Around 1484 patients were registered for follow-up in the previous year. Those with diabetic patients were used to collect their medication on every 2 to 3-month basis. In the outpatient chronic follow up department, approximately 300 adult diabetes mellitus patients were seen weekly. All diabetic patients aged 18 years and older; and who had been on regular follow up treatment for DM regardless of ethnicity and religion were participating in the study. Hearing and/or verbalize impairment, serious illness and newly diagnosed during data collection were excluded from the study.

Participants were hearing and/or verbalizing impairment; those who did not provide coherent answers to the demographic questions. The participant was defined as a serious illness to difficult participate who had a severe medical or psychiatric illness that made it impossible to complete the study questionnaire in one setting, who were requested to terminate the interview for medical reasons, or the data collectors were perceived that the participant was too sick to participate. Participants were newly diagnosed means that they diagnosed before 6 months. This was by considering these participants could be perceived them an inadequacy awareness of the disease to get enough information.

Sample size determination and sampling procedure

The sample size was calculated by assuming a 5% marginal error (d), 95% CI (alpha = 0. 05) and 43.6 the proportion of depression among DM patients [25]. Based on this assumption, the sample size was calculated by the single population proportion formula: n = (Z1t − α/2)2 p (1 − p)/d2; this yields an initial sample size of 378. By considering a 10% non-response rate, 416 diabetic patients were planned and included in the study. A list of diabetic patients was obtained from the outpatient follow up department and used as a sampling frame.

The patients’ records were listed in the follow-up appointment order. Then, the respondents were selected by using a systematic random sampling technique. Based on the decision to collect data for 1 month, the sampling interval was determined by dividing the expected number of diabetic patients per month (1320) into the sample size (416) which gives a sampling interval of three. Thus, every third patient coming to a follow-up service was interviewed until the total sample size was reached.

Data were collected using a face to face interview questionnaire to acquire demographic information; fear of diabetes complications [by using revised fear of complications questionnaire (FCQ)]; and social support (by using Oslo 3-items Social Support Questionnaire). To assess recent clinical related data: fasting plasma glucose level, co-morbidity, diabetes-related complications, duration of diabetes, treatment modality and duration of treatment were collected from the patients’ records by using checklists. The sum of the Oslo 3-items social support scale was ranging from 3 to 14. When social support scale scores were ranged from 3 to 8 is categorized as “poor support”, 9–11 is “moderate support” and 12–14 is “strong support” [26, 27].

Fear of DM-rerated complication questionnaire was assessed specific fears (e.g. blindness, kidney problems, and heart disease, etc.), lifestyle fears, fears of hypoglycemia and future quality of life. It was a self-assessment questionnaire designed to measure fear of complications in diabetes. The items were rated on a four-point scale (0–3), where 0 denotes a low fear of complications and 3 refers to high fear [28]. Perceived low fear of complication was recorded “no” fear of complication whereas perceived high fear of complication also recorded as “yes” had a fear of complication for each item.

Patients with established diabetes mellitus were evaluated for depression by interviewing nine-item of Patient Health Questionnaire nine (PHQ-9) adapted from Pfizer Inc. using local language (Amharic). PHQ-9 is a criteria-based diagnostics tool of depressive disorders and it was also a reliable and valid measure of depression severity. It is a brief questionnaire that scores each of 9 DSM-IV criteria for depression as “0” (not at all) to “3” (nearly every day). PHQ-9 score ≥ 10 had a sensitivity of 88% and specificity of 88% for major depression [29]. PHQ-9 scores of 5, 10, 15, and 20 represent mild, moderate, moderately severe and severe depression, respectively [29, 30].

Since the questionnaire was prepared in English, it was translated into the Amharic language for appropriate and easiness in interviewing the study subjects in the Amharic language. The psychometric properties and cross-cultural validation in the local language of PHQ-9 were validated in Ethiopia [31]. To assure data quality, two weeks before the actual data collection, the questionnaire was pre-tested on 5% of the sample among diabetes patients who were not included in the main study area. Data were collected by four trained, diploma nurses and two supervisors (BSc nurse). Additionally, on each data collection day, the collected data were reviewed and checked for its completeness by principal investigator and supervisors.

Data analysis

Data were entered and edited into EPI-data Version 3.1. The entered data was analyzed by using Statistical Package for Social Science (SPSS) for Windows program version 20. The association was investigated to assess the association between dependent and explanatory variables using binary logistic regression. All explanatory variables with p-value ≤ 0. 20 in the bivariate logistic analysis were fitted into a multivariate logistic regression to identify independently associated factors in the final model. The degree of association was interpreted by using Odds Ratio with 95% confidence interval. The p-value < 0.05 was considered statistically significant.

Results

Socio-demographic characteristics

Four hundred and sixteen study participants were interviewed with a response rate of 100%. Of those, 290 (69.7%) were married, and 120 (28.8%) were governmental employees. Regarding age distributions, the mean and Standard Deviation (SD) age of the participants was 45.5 ± 16.7 years old. Likewise, the median family monthly income of the study participant was 2000 Ethiopian Birr (ETB) (≥ 1401) (Table 1).

Table 1 Socio-demographic characteristics of study participants at Felege Hiwot referral hospital, Bahir Dar, Northwest Ethiopia, 2016 (n = 416)

Clinical characteristics of study participant

About 238 (57.2%) patients were found to have type-II DM. Patients with type-I DM were taken the injectable form of treatment (insulin). Out of 416 participants, 70 (16.8%) participants had a cardiovascular disease (like hypertension) which was evidenced by a review of patients’ cards. Three hundred nineteen (76.7%) and 321 (77.2%) were living with diabetes mellitus and taking physician-prescribed medication at least for 8 years respectively (Table 2).

Table 2 Clinical characteristics of study participants at Felege Hiwot referral hospital, Bahir Dar, Northwest Ethiopia, 2006 (n = 416)

Psychosocial factors attribute to depression in the study participants

Of the total study participant, 213 (51.2%) were reported that they had poor social support. Regarding perceived fear of complication, 222 (53.4%) of respondents had fear of long-term diabetes complication, 109 (26.2%) participants were reported worrying about future problems when their blood sugars were erratic and 171 (41.1%) were worried about losing their eyesight because of diabetes related-complication (Table 3).

Table 3 Psychosocial characteristics of study participants at FHRH, Bahir Dar, Northwest Ethiopia, 2016 (n = 416)

Factors associated with depression

The multivariate logistic regression analysis showed that participants with age 45–54 (AOR = 3.88; 95% CI 1.36, 11.08), being female (AOR = 2.43; (95% CI 1.29, 4.58); who had sexual dysfunction (AOR = 9. 52; 95% CI 2.19, 41.35); those who had moderately support in social life (AOR = 6. 49; 95% CI 2.83, 14.87); who had socially poor supported (AOR = 6. 08; 95% CI 2.98, 12.40); those who were worried about heart disease due to diabetes (AOR = 6. 49; 95% CI 2.22, 18.93) and who had a high fear of kidney problem in their future life (AOR = 6. 12; 95% CI 1.75, 21.23) were more likely had co-morbid depression disorder (Table 4).

Table 4 Logistic regression on the impact of selected socio-demographic, clinical and psychosocial factors, and depression symptoms among diabetes at FHRH, Bahir Dar, Northwest Ethiopia, 2016 (n = 416)

Patients who were 45–54 years had a significantly higher risk of having depression symptoms than those ages less than 45 and greater than 55 years (AOR = 3.88; 95% CI 1.36, 11.08). Females were 2.43 times more likely to develop depressive symptoms as compared to males (AOR = 2.43; (95% CI 1.29, 4.58). Participants who were suffering from sexual dysfunction 9.52 times more likely attack by depression symptoms as compared to those who had no sexual problems (AOR = 9. 52; 95% CI 2. 19, 41.35). There were also significant difference regarding social support; moderate, socially supported were 6.49 times more likely to develop depressive symptoms as compared to those strongly supported (AOR = 6. 49; 95% CI 2.83, 14.87). Patients who had a high fear for kidney problems related to diabetes were 6.12 times more likely to develop depressive symptoms as compared to those who had low fear (AOR = 6.12; 95% CI 1.75, 21.23) (Table 4).

Discussion

To our knowledge, there is high impact of depression and co-morbid diabetes and its importance as a public health problem, little is known about the existence of depression in people with diabetes in the Amhara region, especially in Bahir Dar city. Therefore, this study aimed to assess psychosocial and clinical factors associated with depression among diabetes patients attending FHRH, Bahir Dar Northwest Ethiopia. In this study, age was the significantly associated depression symptom in diabetes patients. The risk factors for depression as per the bivariate analysis in this study were age, being female, presence of sexual dysfunction, moderate and poor social support, high fear of developing cardiac and kidney diseases for their future life.

In this study, age (45–54 years old) 3.88 times has a risk of developing depressive symptoms than those whose age was greater than 54 and less than 45 years old. This finding was alongside with other previous works done in different countries [9,10,11]. In this study, depression was significantly associated with the female gender that was 2.43 times has a risk to develop an attack of depressive symptoms than males. This finding confirms other studies done in Karnataka, Southern India and Peshawar [10, 32, 33].

The results of this study indicated that moderate and poor social support were significantly associated with depression symptoms. Participants who had a lack of social support from their families, neighbors, and friends were around 6.4 times more vulnerable to develop depression symptoms than participants who had strong social support. This finding was in agreement with studies conducted in Iran [14, 20], Croatia [21], Korea [34] and Addis Ababa [17]. This might be due to the effect of social support on emotional well-being (as in receiving love and empathy) and practical help (like the gifts of money, assistance with care). Hence, social support can come from social connectedness, feeling needed, a reassurance of self-worth, reliable support, advice and information, and physical and material assistance.

In our study, depression symptoms 9.52 times increased with the presence of sexual dysfunction in diabetes patients. This finding was supported by other previous studies that reported the presence of complications was strongly associated with depression symptoms in diabetes patients [10], the burden of a lifelong disorder of sexual problems [6]. The nature of diabetes mellitus is producing hyperglycemia, as well as angiopathy, vasculopathy, and neuropathic complication leads to sexual dysfunction in both genders [35]. This might be due to the pathophysiological effect of DM on sexual function through changes in blood supply to the urogenital tissue, reduce to genital lubrication, inability to achieve orgasm, dyspareunia and reduction in libido [36].

But other diabetes clinical risk factors that were significantly associated in varying degree with depression in people with diabetes includes hypertension and microvascular complication [37], diabetic nephropathy [17], physical activities, glucose testing [22], presence of co-morbidities, longer duration of treatment, treatment with insulin [10] and elevated fasting blood sugar level, physical disability and lack of a physician’s advice about lifestyle modifications [32]. Those variables in our study did not significant risk factors to provoke the attack of depressive symptoms in DM patients. This discrepancy might be due to variations in study design and setting, self-care characteristics of respondents, a therapeutic relationship of care provider, sedentary lifestyle of the participants and selection method of respondents.

In this study, high fear of future complication was found to be independently associated with developing depression in diabetes participants. Perceived high fear of cardiac complication with the adjusted odds ratio of 6.49 (2.22, 18.93), and perceived high fear of kidney complications with the adjusted odds ratio of 6.12 (1.75, 21.23) was strongly associated with developing depression. However, other studies were done in Karnataka [10], Iran [9], India [32] and Addis Ababa [17] which found no significant association in terms of fear of complications in diabetes patients. This discrepancy was might be due to almost all other studies that did not investigate the fear of complications. Another possible reason might be earlier studies focused on only demographic, clinical and psychosocial factors related to co-morbid depression in diabetes.

Conclusion

In the current study, clinical factors (sexual dysfunction, sex, and age) and psychosocial factors (social support, fear of complication) were important factors significantly associated with co-morbid depression with patients living diabetes, both type 1 and type 2. To be promoted to optimal medical outcomes and psychological well-being, patient-centered care is essential. Therefore, the health care providers should be availed of a social network of family and friends (because family and friends are a significant source of support for coping mechanisms); providing diabetes education to address patient’s fear of long-term complications by fear reduction and promote survive skill. Sexual function also should be considered an integral part of overall health in diabetic patients.

Strength

The study could be considered as a base for further similar and large-scale studies. The strengths of this study also a significant contribution to the body of knowledge in general and more specifically for health professionals and the patients themselves. Additionally, rather than having to rely on self-report, we were able to use information from patients’ medical diaries to gather information about the presence of diabetes complications, co-morbidity, and FBS levels. Also, we were using a reasonable sample size.

Limitation

Due to the cross-sectional design of this study, it is not possible to draw any conclusion regarding causality. We also assessed level depression and other independent variables by using self-reported question turns to limit this study. Carefully analyzing longitudinal data and mixed design both qualitative and quantitative approaches are the best alternative in the future.

Availability of data and materials

Detailed data will not be shared due to the confidential nature of the data.

Abbreviations

AOR:

Adjusted odd ratio

CI:

Confident interval

DM:

Diabetes mellitus

DSM-IV:

Diagnostic and Statistical of Mental Disorder-5

FCQ:

Fear of Complication Questionnaires

FHRH:

Felege Hiwot Referral Hospital

PHQ-9:

Patent Health Questionnaires Nine

References

  1. 1.

    Atlas D. International diabetes federation IDF Diabetes Atlas. 7th ed. Brussels: International Diabetes Federation; 2015.

    Google Scholar 

  2. 2.

    WHO. W. Global report on diabetes. Geneva: World Health Organization; 2016.

    Google Scholar 

  3. 3.

    Holt RI, de Groot M, Golden SH. Diabetes and depression. Curr Diabetes Rep. 2014;14(6):491.

    Article  CAS  Google Scholar 

  4. 4.

    World Health Organization. Depression: a global crisis. World Mental Health Day. Occoquan: World Federation for Mental Health; 2012.

    Google Scholar 

  5. 5.

    Marcus M, Yasamy MT, van Ommeren MV, Chisholm D, Saxena S. Depression: A global public health concern. 2012.

  6. 6.

    Moulton CD, Pickup JC, Ismail K. The link between depression and diabetes: the search for shared mechanisms. Lancet Diabetes Endocrinol. 2015;3(6):461–71.

    PubMed  Article  Google Scholar 

  7. 7.

    Shoib S, Mushtaq R, Tasleem A, Hayat BM. Depression and diabetes : common link and challenges of developing epidemic !! J Psychiatry. 2015;18(2):14–164.

    Google Scholar 

  8. 8.

    Menezes J, de Morais H, Dias I, Schreiber A, Souza C, da Cunha J. Depression associated with diabetes: from pathophysiology to treatment. Curr Diabetes Rev. 2016;12(3):165–78.

    Article  CAS  Google Scholar 

  9. 9.

    Yekta Z, Pourali R, Yavarian R. Behavioural and clinical factors associated with depression among individuals with diabetes. Eastern Mediterr Health J. 2010;16(3):286–91.

    CAS  Article  Google Scholar 

  10. 10.

    Taranum A, Angadi N, Shakeel M. A study of frequency and factors associated with depression among adult diabetics in urban areas of Davangere. Karnataka Diabetic Foot. 2016;24:26–7.

    Google Scholar 

  11. 11.

    Ganasegeran K, Renganathan P, Manaf RA, Al-Dubai SA. Factors associated with anxiety and depression among type 2 diabetes outpatients in Malaysia : a descriptive cross-sectional single-center study. BMJ BMJ Open. 2014;4(4):e004794.

    PubMed  Article  Google Scholar 

  12. 12.

    Mohamed R, Abdul Kadir A, Yaacob LH. A study on depression among patients with type 2 diabetes mellitus in North-Eastcoast Malaysia. Int J Coll Res Inter Med Public Health. 2012;4(8):1589–600.

    Google Scholar 

  13. 13.

    Agbir MT, Adebowale TO, Audu MD, Goar SG, Puepet FH, Osika MW. Clinical correlates of depression among diabetics in Jos, Nigeria. J Med Trop. 2010;12:1.

    Google Scholar 

  14. 14.

    Behshid G, Reza BM, Samaneh M. Psychosocial contributing factors that affect mental well being in diabetic patients. Russian Open Med J. 2013;2:1.

    Google Scholar 

  15. 15.

    Verma SK, Luo N, Subramaniam M, Sum CF, Stahl D, Liow Chong SA. Impact of depression on health-related quality of life in patients with diabetes. Ann Acad Med Singapore. 2010;39(12):913–7.

    PubMed  Google Scholar 

  16. 16.

    Bahari R. The psychological impact of diabetic limb problems. Int Med J Malaysia. 2015;14(2):3–7.

    Google Scholar 

  17. 17.

    Habtewold TD, Alemu SM, Haile YG. Sociodemographic, clinical, and psychosocial factors associated with depression among type 2 diabetic outpatients in Black Lion General Specialized Hospital, Addis Ababa, Ethiopia: a cross-sectional study. BMC Psychiatry. 2016;16(1):103.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  18. 18.

    Ferreira MC, Piaia C. Clinical variables associated with depression in patients with type 2 diabetes. Revista Brasileira. 2015;61(4):336–40.

    Google Scholar 

  19. 19.

    van Dooren FE, Denollet J, Verhey FR, Stehouwer CD, Sep SJ, Henry RM, Kremers SP, Dagnelie PC, Schaper NC, van der Kallen CJ, Koster A. Psychological and personality factors in type 2 diabetes mellitus, presenting the rationale and exploratory results from The Maastricht Study, a population-based cohort study. BMC Psychiatry. 2016;16(1):17.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  20. 20.

    Yazdi RS, Taslimi Z, Ahmadpanah M, Ghaleiha A. Adjustment to diabetes among diabetic patients: the roles of social support and self-efficacy. Avicenna J Neuro Psych Physio. 2016;3(1): e37470. https://doi.org/10.17795/ajnpp-37470.

    Article  Google Scholar 

  21. 21.

    Pibernik-Okanovic M, Begic D, Peros K, Szabo S, Metelko Z. Psychosocial factors contributing to persistent depressive symptoms in type 2 diabetic patients: a Croatian survey from the European Depression in Diabetes Research Consortium. J Diabetes Compl. 2008;22(4):246–53.

    Article  Google Scholar 

  22. 22.

    Aikens JE. Prospective associations between emotional distress and poor outcomes in type 2 diabetes. Diabetes Care. 2012;35(12):2472–8.

    PubMed  PubMed Central  Article  Google Scholar 

  23. 23.

    Lewko J, Misiak B. Relationships between Quality of Life, Anxiety, Depression, and Diabetes. Ann Depr Anxiety. 2015;2(1):1–2.

    Google Scholar 

  24. 24.

    Young-Hyman D, De Groot M, Hill-Briggs F, Gonzalez JS, Hood K, Peyrot M. Psychosocial care for people with diabetes: a position statement of the american diabetes association: a position statement of the American Diabetes Association. Diabetes Care. 2016;39(12):2126–40.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  25. 25.

    Dejene S, Negash A, Tesfay K, Jobset A, Abera M. Depression, and Diabetes in Jimma University Specialized Hospital, Southwest Ethiopia. J Psychiatry. 2014;17(126):2.

    Google Scholar 

  26. 26.

    Abiola T, Udofia O, Zakari M. Psychometric properties of the 3-item oslo social support scale among clinical students of Bayero University Kano. Nigeria Malaysian J Psychiatry. 2013;22(2):32–41.

    Google Scholar 

  27. 27.

    Dalgard OS, Dowrick C, Lehtinen V, Vazquez-Barquero JL, Casey P, Wilkinson G, Ayuso-Mateos JL, Page H, Dunn G. Negative life events, social support and gender difference in depression. Soc Psychiatry Psychiatr Epidemiol. 2006;41(6):444–51.

    PubMed  Article  Google Scholar 

  28. 28.

    Taylor EP, Crawford JR, Gold AE. Design and development of a scale measuring fear of complications in type 1 diabetes. Diabetes/Metabolism Res Rev. 2005;21(3):264–70.

    Article  Google Scholar 

  29. 29.

    Kroenke K, Spitzer RL, Williams JB. The PHQ-9: Validity of a brief depression severity measure. J Gen Intern Med. 2001;16(9):606–13.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  30. 30.

    Kroenke K, Spitzer RL. The PHQ-9: a new depression diagnostic and severity measure. Psychiatr Ann. 2002;32(9):509–15.

    Article  Google Scholar 

  31. 31.

    Bizuayehu G. Diagnostic Validity of Patient Health Questionnaire-9 and Composite International Diagnostic Interview Assessment Scales for Depression in East Africa (Doctoral dissertation). 2013.

  32. 32.

    Mathew M, Abish A, Kuriakose A, Isaiah JR, Kiran AM, Vijayakumar K. Predictors of depression among patients with diabetes mellitus in Southern India. Asian J Psychiatry. 2013;6(4):313–7.

    Article  Google Scholar 

  33. 33.

    Khan MA, Sultan SM, Nazli R, Akhtar T, Khan MA, Sher N, Aslam H. Depression among patients with type-II diabetes mellitus. J Coll Phys Surg Pak. 2014;24(10):770–1.

    Google Scholar 

  34. 34.

    Lee BJ, Lamichhane DK, Jung DY, Moon SH, Kim SJ, Kim HC. Psychosocial factors and psychological well-being: a study from a nationally representative sample of Korean workers. Industrial Health. 2016;54(3):237–45.

    CAS  PubMed  Article  Google Scholar 

  35. 35.

    Gandhi J, Dagur G, Warren K. Effect of diabetes mellitus on sexual arousal and intercourse. Transl Biomed. 2016;7:2.

    Article  Google Scholar 

  36. 36.

    Meeking DR, Fosbury JA, Cummings MH. Sexual dysfunction and sexual health concerns in women with diabetes. Pract Diabetes. 2013;30(8):327–31.

    Article  Google Scholar 

  37. 37.

    Thour A, Das S, Sehrawat T, Gupta Y. Depression among patients with diabetes mellitus in North India evaluated using patient health questionnaire-9. Indian J Endocrinol Metab. 2015;19(2):252.

    PubMed  PubMed Central  Article  Google Scholar 

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Acknowledgements

We are heart full thank goes to Addis Ababa University for all expenses of the research work, and data collectors and all the study participants who voluntarily participated in this study.

Funding

The study was funded by the Addis Ababa University. The University was critically reviewed and approved the proposal of the study, permitted the study to be conducted, and was involved in data collection process manuscript preparation.

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Authors

Contributions

TWA initiated the idea, carried out the study, and was involved in drafting and editing the manuscript, and interpretation of the data. HG contributed to editing the proposal; critically revised the paper, and provided the final version. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Teshager Woldegiorgis Abate.

Ethics declarations

Ethics approval and consent to participate

This study was approved by Addis Ababa University College of health science Ethical Institutional Review Board committee and ethical approval and clearance were obtained from this committee. Permission and supportive letters were obtained from the respective health bureau and the hospital medical director’s office before actual data collection. Participation was voluntary and information also was collected anonymously after obtaining written consent from each respondent by assuring confidentiality throughout the data collection period. Participants also were told the objective of the study and gave the right to refuse, stop or withdraw at any time of data collection. Patients found to have severe depression were referred to psychiatry clinic for further assessment and treatment.

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Not applicable.

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The authors declare that they have no competing interests.

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Abate, T.W., Gedamu, H. Psychosocial and clinical factors associated with depression among individuals with diabetes in Bahir Dar City Administrative, Northwest Ethiopia. Ann Gen Psychiatry 19, 18 (2020). https://doi.org/10.1186/s12991-020-00267-6

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Keywords

  • Diabetes
  • Depression
  • Adult patient
  • Co-morbidity
  • Factors