The Relationship Between Kidney and Retinal Microvascular Dysfunction in Ghanaians with Type II Diabetes Mellitus
Loading...
Date
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
University of Ghana
Abstract
Background: Globally, the prevalence of diabetes is on the rise, with significant differences
existing between different geographical zones of the world. In 2021, 24 million people in sub
Saharan Africa had diabetes, and this number was expected to more than double by 2045, the
highest projected rise in any region worldwide. A characteristic complication of diabetes is a
microvascular disease that may affect different microcirculation including the retinal and
kidney microcirculation. Based on their common pathophysiological bases, kidney and retinal
microcirculation dysfunction may be related. Therefore, dysfunction in one of these
microcirculations may be used as an auxiliary diagnostic/screening index for the other. Studies
assessing the concordance of kidney microvascular dysfunction (KMD) and retinal
microvascular dysfunction (RMD) in diabetes have yielded inconsistent results, based on the
population studies. Studies assessing the concordance of KMD and RMD in different people
groups including sub-Saharan Africans are lacking. Similar to ethnicity, elevated blood
pressure may be a potential explanatory variable.
General Aim: This study set out to assess the association between KMD and RMD in
Ghanaians with T2D with and without hypertension or suboptimal blood pressure.
Methodology: This was a cross-sectional study among 177 systematically sampled Ghanaians
with T2D aged ≥ 35 years managed at the national diabetes management and research centre
in Accra, Ghana. The sociodemographic and clinical characteristics of the study population
were obtained by the use of a structured questionnaire. Anthropometric and blood pressure
(BP) measurements were obtained by physical examination according to the World Health
Organization’s guidelines. Fasting blood samples were obtained to assess the fasting plasma
glucose, glycated haemoglobin, lipid and creatinine concentrations. KMD was based on
albuminuria, defined as urinary albumin-creatinine ratio ≥ 30mg/g according to the 2012 Kidney Disease: Improving Global Outcomes guidelines. Retinal images were analyzed and
graded under the supervision of a certified ophthalmologist according to the “Early Treatment
Diabetic Retinopathy Study” criteria. Suboptimal BP control was defined per the “2017
American College of Cardiology/American Heart Association” guidelines criteria and
“European Society of Cardiology/European Society of Hypertension” guidelines (for
individuals with hypertension and diabetes) as systolic BP >/= 130mmHg and/or diastolic BP
>/= 80 mmHg 15. The associations of renal and RMD were examined by the use of logistic
regression with adjustments for age, sex, socioeconomic status, diabetes duration, HbA1c,
smoking, systolic BP, obesity, and total cholesterol.
Results: The majority of the study population (77.4%) were females. The mean (±standard
deviation), age, diabetes duration, systolic BP, diastolic BP, body mass index (BMI), HbA1c
concentration, and estimated glomerular filtration rate were 55.93 (±9.35) years, 11.36 (±6.75)
years, 137.32 (±16.55) mmHg, 78.57 (±8.85) mmHg, 30.13 (±5.90) kg/m2, 7.83 (±1.67) % 5.03
(±1.30) mmol/L and 99.84 (±22.45) ml/min/1.73m2 respectively. The prevalence of KMD and
RMD were 27% and 28.8 % respectively. RMD was more prevalent in individuals with KMD
than in those with normal KMD (41.7% vs. 24.0%%, p = 0.026). All cases of moderate or
severe non-proliferative diabetic retinopathy (NPDR) and high-risk or severe proliferative
diabetic retinopathy (PDR) [n=6 (3.4%)] were in the impaired KMD group. In the fully
adjusted model, KMD remained significantly associated with RMD (odds ratio 2.41 [95%
CI:1.00-5.80], p=0.049). The association between KMD and RMD was more pronounced in
individuals with hypertension (3.10[1.01-9.50], 0.048) than without hypertension (1.70[0.33
8.77], 0.523). In analyses stratified by BP levels, KMD was significantly associated with RMD
in individuals with suboptimal BP (2.76[1.07-7.14],0.037) but not in individuals with optimal
BP (0.24[0.00-17.04],0.512) Conclusion: This study shows positive associations between KMD and RMD among
Ghanaians with T2D, with the strength of association, accentuated in individuals with
hypertension/suboptimal BP. Ghanaians with T2D with KMD may benefit from more frequent
evaluation of RMD (and vice-versa), to aid early detection and treatment. Future studies could
further characterize the role of hypertension in the associations between KMD and RMD.
Description
MPhil. Physiology
