Akpalu et al. BMC Psychiatry (2018) 18:357 https://doi.org/10.1186/s12888-018-1933-2 RESEARCH ARTICLE Open Access Depression and glycaemic control among type 2 diabetes patients: a cross-sectional study in a tertiary healthcare facility in Ghana Josephine Akpalu1, Ernest Yorke1, Joana Ainuson-Quampah2, Williams Balogun3 and Kwame Yeboah4* Abstract Background: Diabetes and depression are both chronic debilitating conditions, and their coexistence has been associated with adverse outcomes. In this study, we investigated the association between glycaemic control and depression in type 2 diabetes (T2DM) patients attending a tertiary healthcare facility in Ghana. Methodology: In a cross-sectional study design, Patient Health Questionnare-9 (PHQ-9) was used to assess depression in 400 T2DM, aged 30–65 years. Anthropometric characteristics and blood pressure were measured. Venous blood was collected to measure the levels of glycated haemoglobin (HbA1c). Results: The prevalence of depression was 31.3% among T2DM patients. Female gender, being unmarried, frequent intake of alcohol, previous smoking status and insulin use were associated with increased odds of depression, whereas being educated above basic school level was associated with a decreased odds of depression. In a multivariable logistic regression model, being unmarried and poor glycaemic control were associated with an increase in odds of depression after adjusting for age, gender, and social factors. The association between depression and glycaemic control was attenuated when clinical factors were introduced into the model. Conclusion: In our study population, we found that depression is common among Ghanaians with T2DM, and not associated with poor glycaemic control in a fully multivariable-adjusted model. Keywords: Depression, Type 2 diabetes mellitus, Glycaemic control, Ghana Background developing diabetes, whereas diabetes patients are twice The prevalence of diabetes mellitus has reached epi- as likely to be depressed, compared to non-diabetes in- demic levels globally resulting in enormous human, dividuals [3–5]. economic and social cost worldwide. Currently, 415 The presence of depressive symptoms may affect million people are living with diabetes, 75% of whom T2DM patient’s adherence to diabetes self-care regimen, live in low and middle-income countries; this number particularly diabetic medications, dietary modifications has been projected to increase to 642 million by 2040 and exercise [6]. Compared to non-depressed T2DM [1]. Depression is also a chronic disease that affects patients, depressed T2DM patients have relatively higher about 340 million people at any given time worldwide glycated haemoglobin (HbA1c) and increased prevalence [2]. The temporal relationship between diabetes and de- of microvascular and macrovascular complications [7– pression has been found to be bi-directional; patients 9]. Screening and treatment of depression in diabetes with depression have an increased risk of 1.6 fold of patients have been reported to favourably improve gly- cemic control, as well as prevent or delay diabetes-re- lated complications [4]. However, the recognition and * Correspondence: kyeboah@ug.edu.gh; melvinky@gmail.com 4Department of Physiology, School of Biomedical and Allied Health Sciences, treatment of depression among patients with diabetes University of Ghana, Accra, Ghana have been found to be less than optimum [10]. Moreover, Full list of author information is available at the end of the article © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Akpalu et al. BMC Psychiatry (2018) 18:357 Page 2 of 7 in low and middle-income countries including Ghana, using the formula: weight in kilogrammes divided by there is a dearth of data on the burden of depression the height in metres squared. among diabetes patients [11, 12]. Venous blood was drawn from each participant for In this study, we investigated the association between the measurement of glycated haemoglobin (HbA1c) glycaemic control and depression among T2DM patients using the boronate affinity chromatography method on attending a tertiary care facility in Ghana. We hypothe- PDQ Plus HPLC autoanalyzer (Primus Diagnostics, sized that compared to non-depressed diabetes patients, Trinity Biotech, Ireland). Good glycaemic control was diabetes patients with depression will have poor gly- defined as HBA1c of less than 7% [19]. Ethical approval caemic control. was sought and obtained from the Ethical and Protocol Review Committee of the College of Health Sciences, University of Ghana (Protocol ID MS-Et/M.6-P4.4/ Methodology 2012–13) and each patient provided written voluntary The study was a cross-sectional design, conducted at the informed consent after the rationale and procedure of National Diabetes Management and Research Centre, the study were thoroughly explained. Patients found to Korle Bu Teaching Hospital, Accra, Ghana. The mini- be depressed we referred to the Psychiatry department mum sample size was calculated based on the hypothet- for further assessment and possible management. ical prevalence rates of depression and glycaemic control to be 26% and 15% [13] respectively; 340 patients were Statistical analysis required to achieve a power of 80% and α of 0.05. In all, Data was analysed using SPSS version 18. Data was pre- 400 T2DM patients, aged between 30 and 65 years, were sented as mean with standard deviation for continuous enrolled into the study by systematic random sampling variables and as proportions for categorical variables. of every fourth consenting patient visiting the clinic. Pa- The study subjects were dichotomized based on the tients with type 1 diabetes, pregnant women and those presence or absence of depression. Differences between aged less than 30 years at diagnosis or patients older the two groups with regards to their socio-demographic than 65 years were excluded from the study. In addition, and clinical variables as well as HbA1c were assessed. patients with other causes of depression such as loss of a The chi-squared (χ2) test was used for the comparison close family member within past 4 months and medica- of categorical variables and Students t-test for continu- tion/history of depression or manic/hypomanic episode ous measures. Logistic regression models were per- were excluded from the study. The socio-demographic formed to determine the change in odds of depression characteristics such as age, gender, education, employ- and glycaemic control after adjusting for confounding ment, alcohol & smoking status, as well as clinical data variables. The level of significance was set at p < 0.05. like duration of diabetes, diabetes medication, hyperten- sion and antihypertensive medication were collected Results using structured questionnaires. In our study population with a high representation of Depression was screened using Patient Health females (male: female = 1:4), 125 (31.3%) of the partici- Questionnaire-9 (PHQ-9). The PHQ-9 is an instrument pants were found to have depression. Age, duration of that has been validated in sub-Saharan Africans [14, 15] diabetes and BMI were comparable for T2DM patients and in diabetes patients [16] for the detection of gen- with or without depression (T-test, p-values> 0.05). eral depressive symptoms. The PHQ-9 assesses how Female gender, marital status, educational level, alcohol often the respondent has experienced specific symp- intake and smoking status were associated with depres- toms over the past 2 weeks, assigning values of 0 to 3 sion (χ2, p-values< 0.05). T2DM patients with depression points (0 - not at all, 1 - several days, 2 - more than half had higher systolic blood pressure and glycated haemo- of the days, 3 - nearly every day) [17]. Major depressive globin level than T2DM patients without depression disorder was defined as the presence of at least five (T-test, p < 0.05; Table 1). symptoms, reported for more than half the days in the In unadjusted logistic regression models, being female past 2 weeks, including depressed mood or anhedonia, (OR = 2.84), unmarried (OR = 1.63), regular alcohol con- as well as the thought of suicide or better dead [18]. sumer (OR = 5.47), former smoker (OR = 1.28), using in- Blood pressure was measured after 5 min rest using sulin (OR = 1.3) and having poor glycaemic control (OR = an automated digital blood pressure monitor (Omron 1.82) were associated with an increased odds of depression 907XL pro, Healthcare, Inc., Vernon Hills, IL), with the (Table 2). Multivariable logistic regression models were patients seated comfortably with a back support and constructed to analyze the relationship between depres- arm resting on a table. Body weight and height were sion versus glycaemic control status and marital status, measured with a Seca 740 scale and a stadiometer with sequential adjustments for social and clinical factors. respectively, and the body mass index (BMI) computed Poor glycaemic control was associated with an increase in Akpalu et al. BMC Psychiatry (2018) 18:357 Page 3 of 7 Table 1 General characteristics of participants by depression status T2DM without depression T2DM with depression All Patients Test statistic P N (%) 275 (68.7) 125 (31.3) 400 Age 52.9 ± 8.5 52.2 ± 9 52.7 ± 8.7 t (0.79) 0.48 Duration of diabetes, yrs 9.1 ± 7.3 9.5 ± 6.3 9.2 ± 7 t (0.56) 0.57 Females, n (%) 208 (75.6) 106 (84.6) 314 (78.5) Χ2 (6.72) 0.01 Married n (%) 190 (69.1) 72 (57.6) 262 (65.5) Χ2 (5.02) 0.02 Employed n (%) 194 (70.5) 83 (66.4) 277 (69.2) Χ2 (0.69) 0.41 Education Χ2 (5.04) 0.02 Primary or less 68 (24.7) 41 (32.8) 109 (27.3) Junior grade 119 (43.3) 55 (44) 174 (43.5) High school 50 (18.2) 19 (15.2) 69 (17.3) Tertiary 38 (13.8) 10 (8) 48 (12) Alcohol consumption Χ2 (4.86) 0.035 Doesn’t drink 212 (77.1) 92 (73.6) 304 (76) Occasional 61 (22.2) 21 (16.8) 90 (22.5) Always 2 (0.7) 3 (2.4) 5 (1.3) Smoking status Χ2 (5.48) 0.04 Never 260 (94.5) 116 (92.8) 376 (94) Previous 14 (5.1) 8 (6.4) 22 (5.5) Current 1 (0.4) 1 (0.8) 2 (0.5) BMI (mean ± SD) 30.2 ± 6.6 29.4 ± 5.6 29.9 ± 6.3 t (1.18) 0.24 Obesity classification Χ2 (3.99) 0.076 Normal 56 (20.4) 24 (19.2) 80 (20.1) Overweight 89 (32.4) 41 (32.8) 130 (32.7) Obese 128 (46.5) 60 (48) 188 (47.2) Waist circumferece 99.9 ± 13 99.2 ± 11.7 99.7 ± 12.6 t (0.54) 0.58 WHR 0.93 ± 0.11 0.94 ± 0.09 0.94 ± 0.1 t (0.96) 0.34 Hypertension n (%) 219 (79.6) 99 (79.2) 318 (79.5) 0.39 Systolic BP, mmHg 126 ± 26 133 ± 21 132 ± 23 t (2.16) 0.03 Diastolic BP, mmHg 81 ± 12 80 ± 12 81 ± 12 t (0.77) 0.44 Heart rate, bpm 80 ± 15 81 ± 12 80 ± 14 t (0.71) 0.48 FPG, mol/l 9.2 ± 5.5 9.9 ± 4.3 9.4 ± 5.1 t (1.38) 0.17 HbA1c, % 9.4 ± 2.8 10.2 ± 3 9.9 ± 2.9 t (2.52) 0.013 WHR waist-hip ratio, BMI body mass index, BP blood pressure, FPG fasting plasma glucose, HbA1c glycated haemoglobin, t T-test statistic, Χ2 chi-square statistic odds of depression, even after adjustment for age and with diabetes have twice the odds of developing de- gender (AOR = 1.4, p = 0.037), as well as social factors pression compared with those without diabetes [4, 5]. (AOR = 1.25, p = 0.047); the association was however Depression in T2DM patients has been studied exten- not significant after the introduction of clinical factors sively in populations from high-income countries, into the model (AOR = 1.04, p = 0.286). Being unmar- however, data from lower-income countries such as ried was associated with increased odds of depression Ghana are sparse [11, 12]. in the fully adjusted model (AOR = 1.47, p = 0.046; The prevalence of depression among T2DM patients in Table 3). our study was similar to that reported in other studies. In a meta-analysis of 42 studies involving over 21,000 adult Discussion patients, clinically significant depression was diag- Our study has shown that depression is present in about nosed in 31% of T2DM patients [5]. Comparable re- one-third of T2DM patients after screening, and depres- sults have also been reported among adult patients sion was associated with poor glycaemic control. Patients with diabetes in Greece (33.4%) [20], rural Bangladesh Akpalu et al. BMC Psychiatry (2018) 18:357 Page 4 of 7 Table 2 Unadjusted logistic regression of depression with socio-demographic and clinical factors OR (95% CI) Wald’s p Female gender (Ref: Males) 2.84 (1.67–4.07) 4.59 < 0.001 Age (per 1 year change) 1.303 (0.84–1.68) 1.5 0.13 Duration of diabetes ≥10 years (Ref < 10 yrs) 1.05 (0.81–1.46) 0.32 0.76 Unmarried (Ref: Married) 1.63 (1.05–2.54) 2.17 0.003 Above basic school education (Ref: Basic school) 0.64 (0.4–0.93) 2.07 0.037 Alcohol status (Ref: Never) Occasional 1.1 (0.66–1.74) 0.39 0.711 Always 5.47 (1.56–13.03) 3.14 0.002 Former Smokers (Ref: Non-smokers) 1.28 (1.05–3.84) 0.75 0.041 BMI (ref: Nornal) Overweight 1.07 (0.55–2.1) 0.2 0.851 Obese 0.9 (0.47–1.76) 0.3 0.761 Hypertension (ref: Non-hypertensive) 1.13 (0.87–1.85) 0.63 0.536 Insulin use (Ref: Oral Hypoglycaemic drugs) 1.3 (1.18–1.62) 3.24 0.001 Poor glycaemic control (Ref: HbA1c < 7%) 1.82 (1.32–2.48) 3.72 < 0.001 (30%) [21] and in the UK (25%) [22]. In contrast to patients within the range of 19.4% to 30%. [27–29]. De- our findings, relatively lower prevalence of depression pression in the general population in Ghana was was found in studies from rural Pakistan (14.7%) [23] reported to be rare decades ago, [30] however, in recent and Brazil (18.6%) [24], with a much lower rate in years the prevalence has been shown to be comparable the United States (8.3%) [25]. On the other hand, to that in western countries [30]. The WHO reported a using different depression assessment tools, higher population-based prevalence of mild depression to be rates of depression were reported in urban centers in 6.7% among Ghanaian adults > 50 years of age, far Iran (71.8%) and Pakistan (43.5%) [11, 26]. The wide lower than the findings of the current study [31]. In- variation in depression across various studies may be deed different studies have reported the prevalence of attributed to the difference in the socio-cultural back- depression in different Ghanaian populations to be ground of the participants. In screening for depres- within the range of 3.8 to 9.9% [31–33], and whereas sion in the various these studies, different assessment 24.5% of patients referred to a psychiatry clinic were di- tools with varying sensitivity and specificity to detect agnosed with depression [34]. depression were used [16]. In general, the co-existence of diabetes and depression Very few studies in Africa have evaluated the occur- worldwide has been shown to vary by type of diabetes rence of depression and its effects among patients with and the socio-economic status of populations studied diabetes [12]. However available studies from Nigeria [35]. Depression and other psychological problems tend reported the prevalence of depression among T2DM to be more common in developing countries compared Table 3 Multivariable regression of depression with marital status, medication adherence and glycaemic control Unmarried Wald’s (p) Poor glycaemic control Wald’s (p) Model 1 1.63 (1.15–2.54) 2.42 (0.016) 1.82 (1.32–2.48) 3.72 (< 0.001) Model 2 1.54 (1.1–2.41) 2.16 (0.031) 1.4 (1.27–2.39) 2.09 (0.037) Model 3 1.48 (1.09–2.33) 2.02 (0.042) 1.25 (1.17–2.04) 1.98 (0.047) Model 4 1.46 (1.12–2.31) 2.05 (0.04) 1.04 (0.85–2.29) 0.56 (0.286) Model 5 1.47 (1.11–2.37) 1.99 (0.046) – This Table represents multivariable logistic regression analyses with depression status as dependent variable, and either marital status, medication adherence or glycaemic control as an independent variable in separate models (Model 1). Further adjustments to the models were performed by introducing variables sequentially as indicated below: Model 1: Unadjusted Model 2: Model 1 + age & gender Model 3: Model 2 + social factors (education, employment, alcohol & smoking status) Model 4: Model 3 + clinical factors (duration of diabetes, diabetes medication & hypertension) Model 5: Model 4 + Glycaemic control Akpalu et al. BMC Psychiatry (2018) 18:357 Page 5 of 7 with developed countries [36–38]. Possible explanations the ailing spouse to adhere to diabetes medication and for this observation include higher level of gender self-management practices. Even with married patients, inequalities, social insecurity, lower level of education, Katz [50] reported that the self-management behavior of greater level of poverty and financial constraints among husbands with diabetes often deteriorates when conflict others [37, 38]. Female gender, unmarried status and a exists with their wives. In addition, the belief of a spouse lower level of education, all of which have socio-eco- in the importance of glycemic control predicts such con- nomic implications, were associated with depression in trol better than the patient’s beliefs [49]. However, in this this study. These results are supported by similar find- study, we did not investigate in the quality of intimacy ings in both the general population [37, 38] as well as in married participants, as well as the beliefs of the among people with diabetes [22, 39]. spouse on diabetes management practices. Contrary to various study reports, we did not find sig- nificant association between poor glycaemic control and Limitation of the study depression. Some studies have reported that depressed The major limitation of our study is that the results may T2DM patients have higher HbA1c levels compared not reflect the true burden of depression in the general with non-depressed individuals [25, 40, 41]. The coexist- T2DM population since patients were selected from a ence of depression with diabetes has been reported to be specialized tertiary hospital in urban Ghana. Possible significantly associated with poor glycaemic control [42]. replication of this study in a primary health care setting However, this association has not been demonstrated in in suburban or rural communities to confirm these all studies [43]. In systematic reviews and meta-analysis, findings will be vital. Our study did not include non-dia- depression was found to be weakly correlated with gly- betes controls for comparison, limiting the interpretation caemic status [44]. In type 1 diabetes patients, the asso- of the possible role of diabetes in depression. Also, being ciation between depression and glycaemic control exist a cross-sectional study by design, we cannot deduce the in younger patients, and not in adult patients [45]. The ‘cause-effect’ relationship between diabetes and depres- findings of our study indicate that, clinical factors like sion from our findings; a longitudinal study design will diabetes duration, medication and hypertension status be needed to investigate this relationship. are important factors that link depression to glycaemic status. It must be noted also that predictors of depres- Conclusions sion in non-diabetes population in Ghana has not been The findings of our study have shown that depression is well studied. However, it is worth noting that there is quite common among Ghanaian patients with T2DM. evidence that remission of depression can result in the Poor glycaemic control was not associated with depres- improvement of glycaemic control [7]. In addition, sion among T2DM patients in our study. Marriage was depression is said to impair good self-care practices found to be protective against depression. Future studies resulting in poor adherence to medication, as well as may investigate the role of quality of marital intimacy other diabetes management regimens [46]. Diabetes pa- and spousal beliefs on depression. tients with comorbid depression have been found to have fewer days adherence to dietary, exercise and self- Abbreviations HbA1c: Glycated haemoglobin; MMAS: Morisky Medication Adherence Scale; monitoring recommendations, with a 2.3 fold increased PHQ-9: Patient Health Questionnaire-9; T2DM: Type 2 diabetes mellitus; odds of missing medication doses compared with those WHO: World Health Organization without depression [47]. Acknowledgements The findings of this study indicate that, compared to The authors wish to acknowledge Prof Albert G.B, Amoah, Prof Richard unmarried participants, currently married participants Adanu and Prof Olugbenga Ogedegbe and his team for their tremendous had lower risk prevalence of depression. Studies have support before, during and after this project. We also wish to acknowledge the contributions of Margaret Reynolds and Naa in the acquisition of data. shown marriage is strongly and positively associated with psychological well-being for men and women. On Funding average, the currently married report higher levels of No funding was available for the study. psychological well-being (measured by lower rates of Availability of data and materials depression, substance abuse, and alcoholism) than Data supporting the conclusion of this study is available for systematic review never-married, divorced, widowed, or separated individ- and meta-analysis upon request. uals [48, 49]. Spousal support is among the important Authors’ contributions sources of psychological fortitude during chronic illness JA was involved in the conception, design, acquisition of data, interpretation like diabetes, although there is a possibility of disrup- of data and initial drafting of the manuscript. EY participated in conception, tions in the marital relationship during chronic illness design, acquisition of data and interpretation of data. KY was involved in the conception, design, analysis and interpretation of data. JAQ participated in [48]. The importance of marital support in diabetes the conception, design, acquisition of data and interpretation of data. management might stem from the other spouse helping WB participated in the conception, design and interpretation of data. All Akpalu et al. BMC Psychiatry (2018) 18:357 Page 6 of 7 authors critically reviewed the manuscript for important intellectual 15. Adewuya AO, Ola BA, Afolabi OO. Validity of the patient health content and agreed on the version to be published. questionnaire (PHQ-9) as a screening tool for depression amongst Nigerian university students. J Affect Disord. 2006;96:89–93. Ethics approval and consent to participate 16. van Steenbergen-Weijenburg KM, de Vroege L, Ploeger RR, et al. 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