Gender disparities in diabetes and coronary heart disease medication among patients with type 2 diabetes: results from the DIANA study
- Heike U Krämer†1,
- Elke Raum†1Email author,
- Gernot Rüter2,
- Ben Schöttker1,
- Dietrich Rothenbacher3,
- Thomas Rosemann4,
- Joachim Szecsenyi5 and
- Hermann Brenner1
© Krämer et al.; licensee BioMed Central Ltd. 2012
Received: 23 February 2012
Accepted: 12 July 2012
Published: 27 July 2012
Coronary heart disease (CHD) is one of the most common long-term complications in people with type 2 diabetes. We analyzed whether or not gender differences exist in diabetes and CHD medication among people with type 2 diabetes.
The study was based on data from the baseline examination of the DIANA study, a prospective cohort study of 1,146 patients with type 2 diabetes conducted in South-West Germany. Information on diabetes and CHD medication was obtained from the physician questionnaires. Bivariate and multivariate analyses using logistic regression were employed in order to assess associations between gender and prescribed drug classes.
In total, 624 men and 522 women with type 2 diabetes with a mean age of 67.2 and 69.7 years, respectively, were included in this analysis. Compared to women, men had more angiopathic risk factors, including smoking, alcohol consumption and worse glycemic control, and had more often a diagnosed CHD. Bivariate analyses showed higher prescription of thiazolidinediones and oral combination drugs as well as of angiotensin-converting enzyme (ACE) inhibitors, calcium channel blockers and aspirin in men than in women. After full adjustment, differences between men and women remained significant only for ACE inhibitors (OR = 1.44; 95%-confidence interval (CI): 1.11 – 1.88) and calcium channel blockers (OR = 1.42, 95%-CI: 1.05 – 1.91).
These findings contribute to current discussions on gender differences in diabetes care. Men with diabetes are significantly more likely to receive oral combination drugs, ACE inhibitors and calcium channel blockers in the presence of coronary heart disease, respectively. Our results suggest, that diabetic men might be more thoroughly treated compared to women. Further research is needed to focus on reasons for these differences mainly in treatment of cardiovascular diseases to improve quality of care.
KeywordsMedical management Diabetes mellitus Cardiology
Type 2 diabetes mellitus (T2DM) is a major public health concern. It induces macro- and microvascular damage promoting long-term complications, like coronary heart disease (CHD), stroke or diabetic nephropathy, and is associated with significant morbidity and mortality [1, 2]. The risk of CHD and stroke is altered by age, gender, insulin and glycemic control in patients with diabetes mellitus , but gender-specific differences in the prevalence of cardiovascular diseases (CVD) might also decrease with rising age, especially in older women with diabetes compared to men of the same age .
Diabetes and CVD treatment is complex: besides the different applicable agents, disease status, comorbidities, self-management capabilities and individual compliance of patients have to be considered by the treating physicians [5, 6]. Diabetes treatment is generally intensified if CVD risk factors or comorbidities, such as hypertension, hypercholesterolemia or CHD, are present and vice versa [7, 8].
However, there is evidence that women tend to receive a less adequate therapeutic management than men [9, 10]. Until now, it is still unclear to what extent these gender differences can be explained by confounding factors, such as age, diabetes duration, adherence, prevalent depression or marital status [1, 11].
We aimed to analyze whether or not gender disparities exist in diabetes and CHD medication after controlling for the most important confounding factors in an outpatient population of diabetic patients in Germany.
Study design and study population
This analysis is based on data from the baseline examination of the DIANA study (Type 2 Diabetes Mellitus: New Approaches to Optimize Medical Care in General Practice). DIANA is an epidemiological prospective cohort study with patients with T2DM conducted in the Ludwigsburg-Heilbronn area located in South-West Germany. The study was initiated in 2008 to address (short- and long-term) diabetes-related outcomes and to evaluate potentials for health care improvements in people with T2DM. People with a physician diagnosed T2DM aged 18 and older were recruited consecutively according to a standardized protocol by 38 general practitioners (GP) during regular practice visits between October 2008 and March 2010. The study protocol was approved by the Ethics Committees of the medical faculty of the University of Heidelberg and of the Chamber of Physicians of Baden-Württemberg.
Participating patients completed a self-administered standardized questionnaire at baseline. Information related to diabetes and other medical conditions was reported by the attending physician through a standardized questionnaire. GPs reported all diabetes-relevant physician-diagnosed comorbidities (‘yes’/ ‘no’) and submitted a complete list of all medications currently prescribed. Diabetes medication and CHD medication were classified according to the Anatomic Therapeutic Chemical (ATC) classification system (for more detailed information on classification see Additional file 1).
A blood sample was collected by the GP at time of recruitment and glycated haemoglobin A1c (HbA1c) was assessed by a central laboratory, using ion exchange high pressure liquid chromatography (HPLC) (G8, Tosoh Biosciences).
Definition of key variables
For the following variables information from the GP questionnaire was used and they were defined accordingly: body mass index (BMI) in kg/m², most recent high density lipoprotein level (HDL) in mg/dl and blood pressure (systolic/ diastolic) in mmHg, duration of diabetes and participation in a disease management program for T2DM (DMP-DM). CHD was defined as prevalent CHD or past myocardial infarction. Antidiabetic drugs were differentiated in biguanide, sulfonylurea, alpha-glucosidase inhibitor, thiazolidinedione, glinide, glucagon-like peptide-I (GLP-I) analogue exenatide, dipeptidyl peptidase-4 (DPP-4) inhibitor, oral combination drug (counted as one drug) and insulin treatment in general. Insulins were further specified in short acting human insulin, intermediate acting insulin (basal insulin), (human) insulin combination (short and intermediate acting) and insulin analogue. CHD medication was differentiated in antihypertensive drug, i.e. angiotensin-converting enzyme (ACE) inhibitor, diuretic, beta-blocker, calcium channel blocker and other hypertensive drug, such as angiotensin II receptor blocker, lipid lowering medication and aspirin (see Additional file 1).
The following information was obtained form the participant questionnaires: age at time of recruitment, gender, level of school education, marital status, occupational status, smoking history and alcohol consumption as well as number of appointments with the GP. Information on participants’ self-estimated adherence to all prescribed medications was obtained by the 4-item self-report Morisky medication adherence questionnaire developed . The sum score was calculated ranging from 0 (full adherence) to 4 (poor adherence). Patients were grouped as having a good (zero points), moderate (1 to 2 points) or poor adherence (3 to 4 points). The general health status was evaluated by the first question of the short-form-12 (SF-12) questionnaire .
Classification of glycemic control level was based on baseline HbA1c, defining ≤ 6.4% as good, 6.5% - 7.4% as moderate and ≥7.5% as poor .
When information from the GPs’ was not available (only 3.8% of the participants), information from the participants’ questionnaires was used to minimize missing values, since we found very good agreement of both sources for participants for whom the information of both questionnaires was available (kappa coefficients for medications: >0.90 and for comorbidities: >0.80).
Descriptive statistics included 2-tailed t-tests for means and χ²-tests for proportions comparing differences between men and women. Analyzed covariates were socio-demographic characteristics, glycemic control, smoking status, alcohol consumption, diabetes duration, participation in a DMP-DM and comorbidities. Analyses on prescribed diabetes medication were stratified for gender and differentiated between the presence and absence CHD. Analyses on prescribed CHD medication were stratified for gender and restricted to participants with prevalent CHD. Logistic regression was employed to estimate unadjusted and adjusted odds ratios (ORs) and corresponding 95% confidence intervals (95%-CIs) for describing the association between gender and use of diabetes or CHD medication. In order to adjust for the main independent determinants, variables for multivariate logistic regression models were selected by backward selection separately for each medication group (diabetes and CHD medications). Variables with a p-value < 0.1 were kept in the model to limit potential confounding. Statistical testing was two-sided, an alpha level of 5% was applied, and SAS 9.2 (SAS Institute, Cary, N.C., USA) was used throughout.
Description of the study population
(n = 624)
(n = 522)
Variables of interest
Age in years (mean, SD*)
Age in years
60 - 69
70 - 79
Years of school education
10 - 12
Single/ widowed/ divorced
Body mass index (kg/m²)
25 - <30
30 - <35
Glycemic control by HbA 1c
Moderate (6.5 - 7.4%)
Mean HbA 1c (SD) in %
Mean HDL (SD) in mg/dl
Mean systolic BP (SD) in mmHg
Mean diastolic BP (SD) in mmHg
Physician reported time since diabetes diagnosis
6 – 10 years
11 – 15 years
Appointments with GPs (last 3 months)
2 – 3
Participation in a DMP-DM
General health status (self-rated)
Excellent or very good
Physician diagnosed comorbidities
Coronary heart disease
Diabetes medication by gender and prevalent coronary heart disease
Medication of interest
With coronary heart disease
Without coronary heart disease
(n = 624)
(n = 522)
(n = 147)
(n = 67)
(n = 477)
(n = 455)
Number of diabetes medication (mean, STD*)
Number of diabetes medication
3 and more
Glucagon-like peptide-I analogue (GLP-I) exenatide
Dipeptidyl peptidase-4 (DPP-4) inhibitor
Oral combination drug
Short acting insulin
Intermediate acting (basal insulin)
Human insulin combination (short and intermediate acting)
Coronary heart disease medication by gender and prevalent coronary heart disease
Medication of interest
With coronary heart disease
(n = 624)
(n = 522)
(n = 147)
(n = 67)
Angiotensin-converting enzyme (ACE) inhibitor
Calcium channel blocker
Lipid lowering drug
Results of diabetes and coronary heart disease medication: Odds ratios (95% confidence intervals) for men compared to women (reference)
With coronary heart disease
Without coronary heart disease
1.77 (1.01 - 3.09)
1.73 (0.47 - 1.58)
1.71 (0.91 - 3.21)
1.75 (0.99 - 3.08)
1.58 (0.41 - 6.07)
1.68 (0.89 - 3.17)
1.42 (0.79 - 2.57)1
0.94 (0.28 - 3.17)2
1.52 (0.81 - 2.85)3
Oral combination drug
2.48 (1.51 - 5.34)
2.81 (0.33 - 23.79)
2.45 (1.07 - 5.61)
1.97 (0.94 - 4.13)
1.82 (0.21 - 15.96)
1.91 (0.82 - 4.45)
2.06 (0.98 - 4.31)4
1.93 (0.38 - 9.78)5
1.87 (0.84 - 4.13)6
Coronary Heart Disease Medication
Angiotensin-converting enzyme inhibitor
1.46 (1.14 – 1.86)
2.17 (1.12 – 4.20)
1.52 (1.18 – 1.95)
2.18 (1.09 – 4.35)
1.44 (1.11 – 1.88)7
2.61 (1.26 – 5.42)8
Calcium channel blocker
1.45 (1.10 – 1.91)
2.94 (1.38 – 6.24)
1.55 (1.17 – 2.06)
3.53 (1.58 – 7.89)
1.42 (1.05 – 1.91)9
3.64 (1.55 – 8.52)10
1.52 (1.17 – 1.96)
1.10 (0.58 – 2.08)
1.80 (1.38 – 2.36)
0.96 (0.49 – 1.87)
1.36 (1.01 – 1.84)11
1.12 (0.57 – 2.21)12
Our results demonstrate that men with diabetes were significantly more likely to receive oral combination drugs, ACE inhibitors and calcium channel blockers for CHD than women. Gender-specific differences could also be observed for aspirin use for the overall study sample, but not for the CHD subsample. Taken together, these patterns suggest that diabetic men might be more thoroughly treated than women, especially in terms of CHD medication. Furthermore, the number of diabetes medication was significantly increasing with the level of glycemic control and diabetes duration in men and women with diabetes.
Our finding of gender-specific, also not statistically significant differences in the prescription of diabetes medication such as thiazolidinediones is in accordance with the results of a German cross-sectional study : Lehnert et al. analyzed data on 6,786 people with diabetes in primary care and found a slightly higher prescription rate of thiazolidinediones in men (4.4%) than in women (3.6%) above the age of 60 years. Apart from the different time frames of the studies (Lehnert et al.: 2001; our study: 2008–2010), differences in prescription rates might be mainly explained by disparities in diabetes duration (Lehnert et al.: 4.5 (±1.2 years) vs. our study: 8.8 (±7.1 years)) which is one of the main determinants of treatment choice. Reasons for the higher prescription of thiazolidinediones in men than in women are unclear. Studies have suggested that thiazolidinediones have beneficial effects on inflammatory and atherogenic parameters, blood pressure and microalbuminuria  and that thiazolidinediones doubles the risk of fractures among women, but not among men with diabetes . Due to severe side effects the most frequently prescribed thiazolidinediones, namely Rosiglitazone and Pioglitazone, can no longer be prescribed for diabetes treatment in Germany since April 2011 , and Rosiglitazone was recommended for suspension by the European Medicines Agency (EMA) in September 2010 .
The higher prescription rate of oral combination drugs in men compared to women with T2DM might be explained by the higher number of comorbidities and burden of disease in participating men compared to women and the attempt of the general practitioners to reduce the overall number of medication especially for men.
Our findings regarding CHD medication are in line with previous research: The results of the Euro Heart Survey on Heart Failure including 8,914 patients with heart failure showed that women got less ACE inhibitors and beta-blockers than men . A German cross-sectional study on 1,857 consecutive patients with heart failure likewise showed a difference in the prescription of ACE inhibitors and dosage of beta-blockers, and revealed a less evidence-based treatment in women than in men . For patients with diabetes mellitus, a Swedish study including 229 primary care centres revealed - similar to our study - that men were more often prescribed ACE inhibitors than women and that only one third of the patients below 75 years was on lipid-lowering drug therapy . The higher prescription rate of ACE inhibitors among men can potentially be explained not only by the higher CVD comorbidity, but also by the higher prevalence of nephropathy in men than in women and the protective effect of ACE inhibitors towards progression of nephropathy . Brannström et al  investigated gender disparities in the pharmacological treatment of cardiovascular disease and diabetes mellitus in a cohort of elderly people aged 85 years or older. Women received significantly more drugs, more diuretics, more nitrates. In contrast to our study, no differences were found for insulin therapy, Aspirin and ACE inhibitors, but ACE inhibitor prescription rates were considerably lower in this study compared to ours. For patients with coronary events or revascularisation the EUROASPIRE III study found higher ACE-inhibitors prescription rates for men than for women. Women receive more diuretics, insulin and oral antidiabetic agents . Lipid lowering treatment is generally recommended for all people with T2DM with a high risk for macroangiopathic complications or with CHD . The underuse of lipid lowering drugs together with a lack of antithrombotic drugs might point to a suboptimal quality of health care, because both are crucial for the reduction of cardiovascular comorbidity and all-cause mortality in people with diabetes [27–29]. A large Danish primary care study  on patients screened for diabetes with a high risk for CVD and a large US retrospective study  on people with diabetes found that less women than men received an adequate lipid-lowering treatment. In our study which was conducted between 2008 and 2010, already 43% of the patients with diabetes received lipid lowering drugs, but with no differences between men and women.
In summary, as various studies [32, 33] and a recently published review  point out, gender differences regarding diabetes mellitus are present for all steps in the glucometabolic pathway starting with differences in patho-physiological disturbances, the risk factor distribution, incidence and prevalence of complications, and finally diagnostic techniques and therapy. Franconi et al conclude, that a gender specific approach for all aspects of patient care is much needed to improve overall perspective of patients with diabetes mellitus .
Our study results are limited by the cross-sectional study design, i.e. causality cannot be derived and no conclusion on trends in treatment can be drawn. In particular, our study did not allow identifying with certainty the potential reasons underlying gender differences in medication. The relatively small numbers in each medication group limited the power to detect differences of small and moderate size. Although we aimed for the inclusion of all people with T2DM in a large number of practices, selection effects of participating GPs and regional variation in treatment might limit generalizability. Furthermore, the insurance status was not recorded at baseline. We could not perform a detailed monitoring of completeness of recruitment of diabetes patients in the practices.
Men with diabetes were significantly more likely to receive oral combination drugs, ACE inhibitors and calcium channel blockers in the presence of coronary heart disease. These patterns suggest that diabetic men might be more thoroughly treated than women, especially in terms of CHD medication. We hope that our results will contribute to and stimulate the discussion on gender-specific disparities in diabetes healthcare.
Conflict of interest statement: we declare that we have no conflict of interest. We wish to thank all the participants of the DIANA study and our cooperating study partners. This study was supported by a grant of the Federal Ministry of Education and Research (study identification number: 01GX0746) and is registered at ClinicalTrials.gov (identification number: NCT00742547). The sponsor of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.
This study was supported by a grant of the Federal Ministry of Education and Research (study identification number: 01GX0746).
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