Abstract
Background
Diabetes and psychiatric disorders often co-occur. The prevalence of depression in a person with diabetes is two times higher than that of the general population. During the last decade, the prevalence of diabetes in Vietnam has nearly doubled. However, there is little data regarding depressive symptoms among people with diabetes. Therefore, this study aims to explore the level of depressive symptoms and its associated factors among patients with type 2 diabetes mellitus in Hanoi, Vietnam.
Methodology
A cross-sectional study was conducted among 519 patients diagnosed with type 2 diabetes at the Agricultural General Hospital, one of the largest primary care hospitals for diabetes in Hanoi, Vietnam. Patient Health Questionnaire-9 (PHQ-9) was used to assess the severity of depressive symptoms. Multivariate Tobit and logistic regression models were applied to examine factors associated with the severity of depressive symptoms and medication adherence
Results
Approximately 45.2% of participants were identified as having depressive symptoms at different levels. The proportion of patients with mild, moderate, moderately severe, and severe depressive symptoms is 36.0%, 7.6%, 1.4%, and 0.2% respectively. Regarding the treatment process, patients being treated for their diabetes for a longer time were more likely to have depressive symptoms. Depression was positively linked to currently drinking alcohol (Coef = 1.04; 95% CI = 0.30-1.78), having comorbidities (Coef = 1.08; 95% CI = 0.15; 2.01) and having irregular physical activities (Coef = -1.28; 95% CI = -2.18; -0.38). Patients with severe depressive symptoms (higher PHQ-9 score) were more likely to be non-adherent to their medications in the last month (AOR = 1.30; 95% CI = 1.17; 1.46).
Conclusion
Our study shows that a high percentage of patients with diabetes have depressive symptoms. There is a strong association between having depressive symptoms and non-adherence to medications in the last month. To reduce the risk of developing depressive symptoms, depression should be screened at the initial treatment process and patients should be advised to avoid alcohol and to engage in physical activities regularly.
Keywords: diabetes, depression, depressive symptom, medication adherence, Vietnam
INTRODUCTION
Diabetes is considered a major public health concern which is increasing dramatically in all countries. The estimated number of individuals with diabetes currently stands at 537 million, with projections indicating that this figure will rise to 643 million by 2030 and further increase to 783 million by 2045.1 Nearly 80% of those with diabetes reside in low- and middle-income countries (LMICs), where the prevalence is rising rapidly. About 90% of those with diabetes have type 2 diabetes.2,3 Between 2000 and 2019, there was a 3% increase in diabetes mortality rates by age.4 During the year 2019, diabetes directly resulted in 1.5 million deaths, with nearly half (48%) of those deaths occurring before individuals reached the age of 70.5
Diabetes and psychiatric disorders often co-occur. The prevalence of depression in persons with diabetes is two times higher than that of the general population,6-8 and share a bidirectional relationship. However, psychiatric disorders are commonly undiagnosed or underestimated among people with diabetes.9 People with mental health problems are more likely to experience unhealthy lifestyles (overeating or physical inactivity) which adds to the development of diabetes.6 Meanwhile, the necessity for persons with diabetes to strictly adhere to medication and self-care regimens, and the costs associated with medical care, may lead to psychological impairments.10-12 Both mental disorders and diabetes may negatively affect the quality of life of patients with diabetes.13 Where co-morbidity occurs, it presents significant clinical challenges and worsens the health outcomes of patients.14
The prevalence of psychological problems among patients with diabetes varies across settings. A study assessing depressive symptoms using the Geriatric Depression Scale in elderly patients with diabetes in the National Geriatric Hospital, Hanoi, Vietnam revealed that up to 80% of patients had depressive symptoms,15 whereas only 30.6% of a Japanese sample of elderly patients with diabetes, screened with the Patient Health Questionnaire 9 (PHQ-9)reported depressive symptoms.16 Furthermore, a cross-sectional study from India using the PHQ-9 found that 18% of the participants suffered from moderate (PHQ-9 range from 10 – 14) or severe depression (PHQ-9 ≥20).17
During the last decade, the prevalence of diabetes in Vietnam has nearly doubled, to an alarming level. New diagnoses were most common in young people in urban areas.18 In 2016, one in every 20 people was diagnosed with diabetes, and diabetes was more prevalent in urban than in rural areas.19 However, there is little data regarding depressive symptoms among people with diabetes. Therefore, this study aims to explore the level of depressive symptoms and its associated factors among patients with type 2 diabetes mellitus in Hanoi, Vietnam. This is the first and critical step towards priority setting, implementation, and assessment of a psychological intervention program for patients with diabetes in the community.
METHODOLOGY
Subjects
A cross-sectional study was conducted involving outpatient diabetes patients that were under treatment at the Family Medicine Center (FMC) of the Agricultural General Hospital, Hanoi, Vietnam, one of the largest epicenters that offers health services for patients with diabetes.20
The inclusion criteria were (1) Age 18 years old or above; (2) Diagnosed with type 2 diabetes at least 6 months prior to the study, according to the “Guidelines for Diagnosis and Treatment of Type 2 Diabetes” issued by the Vietnamese Ministry of Health in 2017 (Decision No. 3319/QD-BYT);21 (3) Registered as an outpatient receiving treatment for diabetes in the Department of Outpatient of Agricultural General Hospital; (4) Able to read, write and communicate with the interviewer. We excluded patients who had severe disease conditions or refused to take part in the study. Eligible patients were asked for written informed consent before participating in the study.
The sample size was based on the findings of Hermanns et al., with an estimated 14.1% of patients with diabetes having depressive symptoms. With an α = 0.05 and ε = 0.03, the required sample size was computed to be 517 patients. Anticipating refusal to participate in the study, we invited 519 patients. Convenience sampling was done from the lists of patients who were scheduled for a routine follow-up appointment.
Materials and methods
Following their scheduled routine health appointments, patients were invited to fill out a 20-minute questionnaire, consisting of the following segments: Sociodemographic characteristics such as gender, age, occupation and educational level, and Diabetes treatment-related and health risk behavior characteristics.
Participants were asked about the duration of their diabetes, comorbidities including hypertension, dyslipidemia, heart diseases and lung diseases, alcohol consumption, smoking behaviors, and physical activity.
Patient Health Questionnaire (PHQ-9)
To assess the severity of depressive symptoms among patients with diabetes, the Patient Health Questionnaire (PHQ-9) was used. This tool was formulated based on the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) criteria and the Vietnamese version was shown to be highly valid and reliable.22 The questionnaire has nine items, and each item may be scored from 0 to 3; therefore, the total score may range from 0 to 27.
The following cut-offs were used to classify depression severity: 0–4 points is normal, 5–9 points is mild, 10–14 points is moderate, 15–19 points is moderate-severe, and ≥20 points is severe. Patients with scores higher than 4 were considered as “having depressive symptoms.”23
The questionnaire was piloted on 20 volunteers (also outpatient diabetes), resulting in minor changes in the wording of diabetes treatment-related characteristics. During the study, the questionnaire was administered by a final-year nursing student, who had been well-trained regarding the study objectives, the questionnaire, and how to collect data.
Statistical analysis
Multivariate Tobit and logistic regression models were applied to examine factors associated with the severity of depressive symptoms and medication adherence. To identify the reduced regression model, we added a forward stepwise selection strategy with a threshold of less than 0.2. A p-value less than 0.05 was considered statistically significant. Pearson’s chi-square test was used for categorical variables, and the Mann-Whitney U test was used for non-parametric continuous variables for comparing demographic characteristics, and health risk behaviors of participants between those who have and those who do not have depressive symptoms. All data analyses were done using STATA software version 12 (Stata Corp. LP, College Station, United States of America).
Ethics approval
Ethics approval was obtained from the Institutional Review Board of Hanoi University of Public Health number 316/2021/YTCC-HD3 on the 12th of July 2021.
RESULTS
The socioeconomic characteristics of patients with diabetes are presented in Table 1. Of the 519 type 2 out-patients with diabetes invited to the study, 516 (99.4%) participated. Most participants finished secondary school (48.6%), retired (63.2%), and enrolled in a compulsory public health insurance scheme (78.7%). There were 231 patients (44.8%) with depression symptoms, ranging from mild to severe levels (PHQ-9 ≥5).
Table 1.
Socio-economic characteristics
| Having depressive symptoms | p | ||||||
|---|---|---|---|---|---|---|---|
| Yes | No | Total | |||||
| n | % | n | % | n | % | ||
| Total | 231 | 44.8 | 285 | 55.2 | 516 | 100 | |
| Gender | |||||||
| Male | 95 | 41.1 | 125 | 43.9 | 220 | 42.6 | 0.53 |
| Female | 136 | 58.9 | 160 | 56.1 | 296 | 57.4 | |
| Educational level | |||||||
| Under secondary school | 44 | 19.1 | 49 | 17.2 | 93 | 18.0 | 0.42 |
| Secondary school | 117 | 50.7 | 134 | 47.0 | 251 | 48.6 | |
| Higher than secondary school | 70 | 30.3 | 102 | 35.8 | 172 | 33.3 | |
| Occupation | |||||||
| Employed | 70 | 30.3 | 93 | 32.6 | 163 | 31.6 | 0.30 |
| Unemployed | 16 | 6.9 | 11 | 3.9 | 27 | 5.2 | |
| Retired | 145 | 62.8 | 181 | 63.5 | 326 | 63.2 | |
| Health insurance | |||||||
| Obligation | 172 | 74.5 | 234 | 82.1 | 406 | 78.7 | 0.04*a |
| Volunteer | 59 | 25.5 | 51 | 17.9 | 110 | 21.3 | |
| Mean | SD | Mean | SD | Mean | SD | p | |
| Age | 68 | 9.0 | 66 | 8.0 | 67 | 9.0 | 0.03*b |
| Distance to health facility (km) | 5.6 | 5.4 | 5.2 | 4.7 | 5.4 | 5.1 | 0.03*b |
Note: Italicized values are significant at
p <0.05;
from Pearson’s chi-squared test p-value;
from Mann-Whitney U test p-value for non-parametric variables.
While the study could not find a significant difference in the educational level and occupation of surveyed patients with diabetes, health insurance schemes of the two groups were significantly different.
Patients with diabetes with depressive symptoms were older and lived farther from health facilities than patients without depressive symptoms (p<.05). The mean age of the whole sample size was 67 years old (SD = 9.0) and those who were depressed were statistically significantly older than those who did not have depression (68 and 66 years old respectively). The distance to health facilities between the two groups showed the same result, and the mean distance was 5.4 km (SD = 5.1).
Table 2 highlights the clinical-related symptoms and health risk behaviors of patients with diabetes. About 10% and more than 15% of participants currently smoked and drank alcohol respectively. The majority of the participants (84.0%) engaged in daily physical activities. The prevalence of comorbidities was high (90.3%) and 16.7% of patients reported having side effects from their medications within the last 3 months. Regarding disease symptoms, 17.1% of patients reported headache, dizziness and about one-third had numbness of the limbs. Approximately 10% of the participants reported forgetting to take their medications within the last month. The mean duration of the disease was 8.0 years (SD = 6.5) and the mean BMI was 22.8 (SD = 2.8). Only alcohol drinking was found to be significantly different between groups.
Table 2.
Clinical-related symptoms and health risk behavior
| Having depressive symptoms | p | |||||||
|---|---|---|---|---|---|---|---|---|
| Yes | No | Total | ||||||
| n | % | n | % | n | % | |||
| Smoking | 0.27 | |||||||
| Never smoking | 186 | 80.5 | 214 | 75.1 | 400 | 77.5 | ||
| Former smoking | 23 | 10.0 | 41 | 14.4 | 64 | 12.4 | ||
| Currently smoking | 22 | 9.5 | 30 | 10.5 | 52 | 10.1 | ||
| Drinking alcohol | 0.04*a | |||||||
| Never drinking | 186 | 81.9 | 206 | 72.8 | 392 | 76.9 | ||
| Former drinking | 13 | 5.7 | 21 | 7.4 | 34 | 6.7 | ||
| Currently drinking | 28 | 12.3 | 56 | 19.8 | 84 | 16.5 | ||
| Physical activity | 0.27 | |||||||
| Several times per month | 24 | 8.8 | 28 | 13.2 | 52 | 10.7 | ||
| Several times per week | 16 | 5.8 | 10 | 4.7 | 26 | 5.3 | ||
| Everyday | 234 | 85.4 | 175 | 82.2 | 409 | 84.0 | ||
| Other people in family having diabetes | 63 | 22.7 | 53 | 23.4 | 116 | 23.0 | 0.86 | |
| Comorbidities | 208 | 88.1 | 174 | 93.1 | 382 | 90.3 | 0.09 | |
| Disease symptoms | ||||||||
| Unexplained weight loss | 14 | 4.9 | 18 | 7.8 | 32 | 6.2 | 0.18 | |
| Headache, dizzy | 55 | 19.3 | 33 | 14.3 | 88 | 17.1 | 0.13 | |
| Numbness of the limbs | 102 | 35.8 | 73 | 31.6 | 175 | 33.9 | 0.32 | |
| Forgot to take pills last month | 22 | 8.2 | 24 | 11.2 | 46 | 9.5 | 0.28 | |
| Side effect of medicine within last 3 months | 42 | 14.7 | 44 | 19.1 | 86 | 16.7 | 0.19 | |
| Mean | SD | Mean | SD | Mean | SD | p | ||
| Duration of disease (year) | 8.6 | 6.9 | 7.6 | 6.1 | 8.0 | 6.5 | 0.13 | |
| BMI | 22.8 | 2.7 | 22.9 | 2.8 | 22.8 | 2.8 | 0.70 | |
Note: Italicized values are significant at
p<0.05
from Pearson’s chi-square test p-value
Table 3 indicates the depressive symptom characteristics of patients with diabetes. About 36.0% of participants were classified as having mild depressive symptoms, while 10% scored worse (PHQ-9 ≥10). The percentage of patients experiencing moderate, moderate-severe and severe depressive symptoms were 7.6%, 1.4% and 0.2%, respectively. The mean score of PHQ-9 was 5.0 (SD = 2.9), which is in the range of ‘mild’ symptoms.
Table 3.
Level of depressive symptoms among diabetic patients
| Frequency (n) | Percentage (%) | |
|---|---|---|
| Normal | 283 | 54.8 |
| Mild | 186 | 36.0 |
| Moderate | 39 | 7.6 |
| Moderate severe | 7 | 1.4 |
| Severe | 1 | 0.2 |
| Mean | SD | |
| PHQ-9 score | 5.0 | 2.9 |
Figure 1 depicts the mean score of PHQ-9 plotted against disease duration. The mean PHQ score was relatively constant (i.e., 5 points) among those having diabetes for 0-20 years but gradually increased thereafter.
Figure 1.
The mean of PHQ-9 score for the duration of diabetes.
The results of the multivariate regression models to identify factors associated with having depressive symptoms are shown in Table 4. Older people have more depressive symptoms (Coef = 0.05; 95% CI = 0.01-0.08). Patients who currently drink alcohol were more likely to have higher depressive symptoms compared to those who never use alcohol (Coef = 1.04; 95% CI = 0.30-1.78). In terms of physical activity, exercising several times a week or every day was also associated with a lower score of PHQ-9 (Coef = -0.96; 95% CI = -2.33; -0.42 and Coef = -1.28; 95% CI = -2.18; -0.38, respectively). By contrast, participants with comorbidities had a higher likelihood of having depressive symptoms than those who did not (Coef = 1.08; 95% CI = 0.15; 2.01).
Table 4.
Factors associated with having depressive symptoms among diabetic patients
| PHQ9 score | ||
|---|---|---|
| Coef | 95% CI | |
| Age | 0.05** | 0.01; 0.08 |
| Drinking alcohol (vs never) | ||
| Currently drinking | 1.04** | 0.30; 1.78 |
| Physical activity (vs several times a month) | ||
| Several times a week | -0.96* | -2.33; -0.42 |
| Everyday | -1.28** | -2.18; -0.38 |
| Comorbidities | 1.08* | 0.15; 2.01 |
Note: Italicized values are significant at
p<0.05,
p<0.01.
Table 5 shows the factors associated with medication adherence among patients with diabetes. Notably, patients having more severe depressive symptoms (higher PHQ-9 scores) were more likely to forget taking their medication in the last month (AOR=1.30; 95% CI = 1.17; 1.46). Being female and being older was associated with non-adherence to medication in the previous month (AOR=0.45; 95% CI = 0.20; 0.05 and AOR=0.95; 95% CI = 0.91-0.99, respectively). By contrast, those who currently drink alcohol, have numbness of the limbs, and experienced side effects from medicine within the last 3 months had a lower likelihood of sufficiently adhering to medication.
Table 5.
Factors associated with medication adherence among diabetic patients
| Missed medication last month (Yes vs No) | ||
|---|---|---|
| AOR | 95%CI | |
| Gender (female vs male) | 0.45* | 0.20; 0.50 |
| Age | 0.95* | 0.91; 0.99 |
| Health insurance (volunteer vs obligation) | 0.35* | 0.12; 0.99 |
| Drinking alcohol (vs never) Currently drinking | 1.41* | 1.13; 1.51 |
| Depressive symptom | 1.30** | 1.17; 1.46 |
| Numbness of the limbs (yes vs no) | 1.48* | 1.17; 1.60 |
| Side effect of medicine within last 3 months (yes vs no) | 2.63** | 1.10; 6.30 |
Note: Italicized values are significant at
p<0.05,
p<0.01.
DISCUSSION
Our study provided valuable evidence on the level of depression among diabetes patients in a primary setting in Vietnam. We found that nearly half of the patients suffered from mild to severe depressive symptoms. Moreover, depressive symptoms increased gradually from the early to the late stage of the treatment process. Currently drinking alcohol and having comorbidities were positively associated with more severe depression while doing physical activities related to lower PHQ-9 scores. Notably, patients with a higher level of depressive symptoms were more likely to forget to take their medicine in the last month.
The percentage of participants having depressive symptoms in our study was lower than that of other studies in Vietnam15 and in other countries.16-24 The difference can be explained by the variation of individual characteristics in our sample. We enrolled patients with diabetes aged 18 and above, while other studies collected data on elderly patients only. When compared to patients having chronic diseases such as cardiovascular disorders, results from our study are similar to previous studies,25,26 Diabetes and cardiovascular disease are the most common chronic diseases,27 for which patients have to undergo long treatment duration and strict compliance to a treatment regimen.
Regarding treatment duration, we found that patients who had long-standing diabetes were more likely to have depressive symptoms. At the start of the treatment process, they likely had to adapt to rigorous treatment procedures, which might have contributed to the development of depressive symptoms.28-29 Moreover, patients with diabetes have to live with the condition for the rest of their lives,30 therefore, they are more likely to have more severe depressive symptoms later in the treatment process.
Our study also emphasized aging in mental health problems. As prolonged diabetic treatment has been positively associated with an accelerated aging process, age-related comorbidities may reduce brain function and trigger several symptoms of depression.15 Thus, an intervention that reduces depressive symptoms among patients with diabetes should focus on elderly patients or patients at the later stages of treatment.
The findings from our study are similar to several previous research in the association between persons with diabetes using alcohol and having depressive symptoms.31 Heavy alcohol use is more common in those who are more depressed than among the general population.32 On the other hand, there is evidence that chronic alcohol use causes high depressive symptoms.33
The study also revealed that having comorbidities were related to having depressive symptoms. Given that heavy alcohol use may increase the risk of having cardiovascular comorbidities, individuals who have both problems may have a higher risk of depression.34
In contrast, physical activity was associated with a lower level of depressive symptoms. Regular exercise is considered to have a positive effect in preventing the development of chronic diseases, as well as decreasing the likelihood of depression and alleviating mental stress.35 Among patients with diabetes, physical activity also supports maintaining normal glucose uptake which contributes to better glucose control.36
Notably, a higher level of depressive symptoms was related to a higher likelihood of not taking medicine. This is in line with previous studies exploring the impact of depression on adherence to diabetic medication.10,37 Compared with other patients, persons with diabetes were at a higher risk of experiencing depression and anxiety disorders.38 Moreover, stressors and depressive symptoms are associated with medication nonadherence.39 To reduce the long-term complications of diabetes, continuous medical care, self-management, and adherence to prescribed medication are required.40 Therefore, earlier assessment of mental health problems among patients with diabetes will limit adverse effects and reduce the risk of long-term complications during the treatment process.
Several implications can be drawn from our study. As the level of depressive symptoms was found to be associated with non-adherence to medication, a comprehensive health-care program should integrate physical and psychological examination. Screening and intervention for depression should be initiated early in the treatment process to minimize the development of depressive symptoms later in the disease course, alongside limiting complications and providing psychological support. Avoiding alcohol and engaging in regular physical activities play an essential role in reducing the risk of developing depressive symptoms.
Nevertheless, our study has some limitations. First, self-reported information may lead to recall bias and social desirability bias. In order to minimize these, we excluded interviewers who were affiliated with the hospital. In addition, the instructions, as well as the purposes of the study, were explained clearly to the participants. Second, the cross-sectional study design may reduce the causal inferences between having depressive symptoms and non-adherence to medication. Finally, the generalizability of study results to other international populations can be limited due to the convenience sampling technique.
CONCLUSION
Our study reveals that a great number of patients with diabetes have depressive symptoms. There is a strong association between having depressive symptoms and non-adherence to medication in the last month. To reduce the risk of developing depressive symptoms, depression should be screened for during the initial treatment process and patients should be advised to avoid alcohol and engage in regular physical activities.
Statement of Authorship
The authors certified fulfillment of ICMJE authorship criteria.
CRediT Author Statement
KTN: Conceptualization, Methodology, Software, Formal analysis; Writing – original draft preparation; HPN: Conceptualization, Methodology, Writing – original draft preparation; KVB: Writing – review and editing; JW: Conceptualization, Methodology, Writing – original draft preparation.
Author Disclosure
The authors declared no conflict of interest.
Funding Source
None.
References
- 1.International Diabetes Federation . IDF Diabetes Atlas, 10th edition. Brussels, Belgium; 2021. [Google Scholar]
- 2.International Diabetes Federation . IDF Diabetes Atlas, 9th edition. Brussels, Belgium; 2019. [Google Scholar]
- 3.Moucheraud C, Lenz C, Latkovic M, Wirtz VJ. The costs of diabetes treatment in low- and middle-income countries: A systematic review. BMJ Global Health 2019;4(1):e001258. PMID: . PMCID: . 10.1136/bmjgh-2018-001258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.World Health Organization . Diabetes Fact Sheet. 2023. [Google Scholar]
- 5.Global Burden of Disease Collaborative Network . Global Burden of Disease Study 2019. Results. Institute for Health Metrics and Evaluation. 2020. https://www.healthdata.org/research-analysis/gbd. [Google Scholar]
- 6.Ali S, Stone MA, Peters JL, Davies MJ, Khunti K. The prevalence of co-morbid depression in adults with Type 2 diabetes: A systematic review and meta-analysis. Diabet Med. 2006;23(11):1165–73. PMID: 17054590 10.1111/j.1464-5491.2006.01943.x. [DOI] [PubMed] [Google Scholar]
- 7.Perrin NE, Davies MJ, Robertson N, Snoek FJ, Khunti K. The prevalence of diabetes-specific emotional distress in people with type 2 diabetes: A systematic review and meta-analysis. Diabet Med. 2017;34:1508–20. PMID: . 10.1111/dme.13448. [DOI] [PubMed] [Google Scholar]
- 8.Semenkovich K, Brown ME, Svrakic DM, Lustman PJ. Depression in type 2 diabetes mellitus: Prevalence, impact, and treatment. Drugs. 2015;75(6):577–87. PMID: . 10.1007/s40265-015-0347-4. [DOI] [PubMed] [Google Scholar]
- 9.Pouwer F, Kupper N, Adriaanse MC. Does emotional stress cause type 2 diabetes mellitus? A review from the European Depression in Diabetes (EDID) Research Consortium. Discov Med. 2010;9(45):112–8. PMID: . [PubMed] [Google Scholar]
- 10.Ciechanowski PS, Katon WJ, Russo JE. Depression and diabetes: Impact of depressive symptoms on adherence, function, and costs. Arch Intern Med. 2000;160(21):3278–85. PMID: . 10.1001/archinte.160.21.3278. [DOI] [PubMed] [Google Scholar]
- 11.Black SA. Increased health burden associated with comorbid depression in older diabetic Mexican Americans. Results from the Hispanic Established Population for the Epidemiologic Study of the elderly survey. Diabetes Care. 1999;22(1):56–64. PMID: . 10.2337/diacare.22.1.56. [DOI] [PubMed] [Google Scholar]
- 12.Katon W, Russo J, Lin EH, et al. Depression and diabetes: Factors associated with major depression at five-year follow-up. Psychosomatics 2009;50(6):570–9. PMID: . PMCID: . 10.1176/appi.psy.50.6.570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Lustman PJ, Anderson RJ, Freedland KE, de Groot M, Carney RM, Clouse RE. Depression and poor glycemic control: A meta-analytic review of the literature. Diabetes Care. 2000;23(7):934–42. PMID: . 10.2337/diacare.23.7.934. [DOI] [PubMed] [Google Scholar]
- 14.Moussavi S, Chatterji S, Verdes E, Tandon A, Patel V, Ustun B. Depression, chronic diseases, and decrements in health: Results from the World Health Surveys. Lancet. 2007;370(9590):851–8. PMID: . 10.1016/S0140-6736(07)61415-9. [DOI] [PubMed] [Google Scholar]
- 15.Vu HTT, Nguyen TX, Nguyen HTT, et al. Depressive symptoms among elderly diabetic patients in Vietnam. Diabetes Metab Syndr Obes. 2018;11:659–65. PMID: . PMCID: . 10.2147/DMSO.S179071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Ishizawa K, Babazono T, Horiba Y, et al. Uchigata Y. The relationship between depressive symptoms and diabetic complications in elderly patients with diabetes: Analysis using the Diabetes Study from the Center of Tokyo Women’s Medical University (DIACET). J Diabetes Complications. 2016;30(4):597–602. PMID: . 10.1016/j.jdiacomp.2016.02.004. [DOI] [PubMed] [Google Scholar]
- 17.Raval A, Dhanaraj E, Bhansali A, Grover S, Tiwari P. Prevalence and determinants of depression in type 2 diabetes patients in a tertiary care centre. Indian J Med Res. 2010;132:195–200. PMID: . [PubMed] [Google Scholar]
- 18.Le NTD, Dinh Pham L, Quang Vo T. Type 2 diabetes in Vietnam: A cross-sectional, prevalence-based cost-of-illness study. Diabetes Metab Syndr Obes. 2017;10:363–74. PMID: . PMCID: . 10.2147/DMSO.S145152. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Pham NM, Eggleston K. Prevalence and determinants of diabetes and prediabetes among Vietnamese adults. Diabetes Res Clin Pract. 2016;113:116–24. PMID: . 10.1016/j.diabres.2015.12.009. [DOI] [PubMed] [Google Scholar]
- 20.Agricultural General Hospital . Workshop ‘Integrating Family Medicine activities at the General Hospital of Agriculture [Internet] 2018. [cited 27 March 2020]. http://benhviendakhoanongnghiep.vn/hoi-thao-long-ghep-hoat-dong-y-hoc-gia-dinh-tai-benh-vien-da-khoa-nong-nghiep.
- 21.Vietnam Ministry of Health . Decision No. 3319/QD-BYT stipulating guideline on diagnosis and treatment for type 2 diabetes; 2017. [Google Scholar]
- 22.Tran BX, Dang AK, Truong NT, et al. Depression and quality of life among patients living with HIV/AIDS in the era of universal treatment access in Vietnam. Int J Environ Res Public Health. 2018;15(12):2888. PMID: . PMCID: . 10.3390/ijerph15122888. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Thanh DD. Preliminary assessment of patients’ health questionnaire (PHQ-9) in screening for depressed patients. Practical medical journal. 2011;774:173–6. [Google Scholar]
- 24.Khan ZD, Lutale J, Moledina SM. Prevalence of depression and associated factors among diabetic patients in an outpatient diabetes clinic. Psychiatry J. 2019;2019:2083196. PMID: . PMCID: . 10.1155/2019/2083196. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Peltzer K, Pengpid S. Anxiety and depressive features in chronic disease patients in Cambodia, Myanmar and Vietnam. S Afr J Psychiatr. 2016;22(1):940. PMID: . PMCID: . 10.4102/sajpsychiatry.v22i1.940. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Daré LO, Bruand P-E, Gérard D, et al. Co-morbidities of mental disorders and chronic physical diseases in developing and emerging countries: A meta-analysis. BMC Public Health. 2019;19(1):304. PMID: . PMCID: . 10.1186/s12889-019-6623-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Clarke DM, Currie KC. Depression, anxiety and their relationship with chronic diseases: A review of the epidemiology, risk and treatment evidence. Med J Aust. 2009;190(S7):S54–60. PMID: . https://doi.org.10.5694/j.1326-5377.2009.tb02471.x. [DOI] [PubMed] [Google Scholar]
- 28.Nguyen HTT, Moir MP, Nguyen TX, et al. Health-related quality of life in elderly diabetic outpatients in Vietnam. Patient Prefer Adherence. 2018;12:1347–54. PMID: . PMCID: . 10.2147/PPA.S162892. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Dao-Tran TH, Anderson D, Chang A, Seib C, Hurst C. Factors associated with self-management among Vietnamese adults with type 2 diabetes. Nurs Open. 2018;5(4):507–16. PMID: . PMCID: . 10.1002/nop2.158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Bhatti Z, Salek M, Finlay A. Chronic diseases influence major life changing decisions: A new domain in quality of life research. J R Soc Med. 2011;104(6):241–50. PMID: . PMCID: . 10.1258/jrsm.2011.110010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Knychala MA, Jorge ML, Muniz CK, Faria PN, Jorge PT. High-risk alcohol use and anxiety and depression symptoms in adolescents and adults with type 1 diabetes mellitus: A cross-sectional study. Diabetol Metab Syndr. 2015;7:24. PMID: . PMCID: . 10.1186/s13098-015-0020-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Currie SR, Patten SB, Williams JV, et al. Comorbidity of major depression with substance use disorders. Can J Psychiatry. 2005;50(10):660–6. PMID: . 10.1177/070674370505001013. [DOI] [PubMed] [Google Scholar]
- 33.Boden JM, Fergusson DM. Alcohol and depression. Addiction. 2011;106(5):906–14. PMID: . 10.1111/j.1360-0443.2010.03351.x. [DOI] [PubMed] [Google Scholar]
- 34.Elgendy R, Deschênes SS, Burns RJ, Levy M, Schmitz N. Alcohol consumption, depressive symptoms, and the incidence of diabetes-related complications. J Diabetes. 2019;11(1):14–22. PMID: . 10.1111/1753-0407.12822. [DOI] [PubMed] [Google Scholar]
- 35.Kim DJ. Effects of physical activity on depression in adults with diabetes. Osong Public Health Res Perspect. 2018;9(4):143–9. PMID: . PMCID: . 10.24171/j.phrp.2018.9.4.02. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Camacho RC, Galassetti P, Davis SN, Wasserman DH. Glucoregulation during and after exercise in health and insulin-dependent diabetes. Exerc Sport Sci Rev. 2005;33(1):17–23. PMID: . [PubMed] [Google Scholar]
- 37.Lunghi C, Zongo A, Moisan J, Grégoire JP, Guénette L. The impact of incident depression on medication adherence in patients with type 2 diabetes. Diabetes Metab. 2017;43(6):521–8. PMID: . 10.1016/j.diabet.2017.07.003. [DOI] [PubMed] [Google Scholar]
- 38.Gonzalez JS, Safren SA, Cagliero E, et al. Depression, self-care, and medication adherence in type 2 diabetes: Relationships across the full range of symptom severity. Diabetes Care. 2007;30(9):2222–7. PMID: . PMCID: . 10.2337/dc07-0158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Mayberry LS, Egede LE, Wagner JA, Osborn CY. Stress, depression and medication nonadherence in diabetes: Test of the exacerbating and buffering effects of family support. J Behav Med. 2015;38(2): 363–71. PMID: . PMCID: . 10.1007/s10865-014-9611-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Al-Hayek AA, Robert AA, Alzaid AA, et al. Association between diabetes self-care, medication adherence, anxiety, depression, and glycemic control in type 2 diabetes. Saudi Med J. 2012;33(6):681–3. PMID: . [PubMed] [Google Scholar]

