1. Heritability and Genetics of Type 2 Diabetes Mellitus in Sub-Saharan Africa: A Systematic Review and Meta-Analysis
- Author
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Christian Obirikorang, Enoch Odame Anto, Edwin Ferguson Laing, Emmanuel Acheampong, Max Efui Annani-Akollor, Evans Adu Asamoah, and Eddie-Williams Owiredu
- Subjects
Candidate gene ,endocrine system diseases ,Endocrinology, Diabetes and Metabolism ,Population ,Review Article ,Biology ,Sulfonylurea Receptors ,Polymorphism, Single Nucleotide ,Diseases of the endocrine glands. Clinical endocrinology ,Endocrinology ,Humans ,Genetic Predisposition to Disease ,Family history ,Potassium Channels, Inwardly Rectifying ,Pyrophosphatases ,education ,Africa South of the Sahara ,Genetics ,education.field_of_study ,Haptoglobins ,Phosphoric Diester Hydrolases ,Tumor Necrosis Factor-alpha ,nutritional and metabolic diseases ,Odds ratio ,Heritability ,RC648-665 ,Study heterogeneity ,Diabetes Mellitus, Type 2 ,Meta-analysis ,Adiponectin ,TCF7L2 ,Transcription Factor 7-Like 2 Protein - Abstract
Objectives. Sub-Saharan Africa (SSA) is observing an accelerating prevalence rate of type 2 diabetes mellitus (T2DM) influenced by gene-environment interaction of modifiable and nonmodifiable factors. We conducted a systematic review and meta-analysis on the heritability and genetic risk of T2DM in SSA. Methods. We reviewed all published articles on T2DM in SSA between January 2000 and December 2019 and available in PubMed, Scopus, and Web of Science. Studies that reported on the genetics and/or heritability of T2DM or indicators of glycaemia were included. Data extracted included the study design, records of family history, pattern and characteristics of inheritance, genetic determinants, and effects estimates. Results. The pattern and characteristics of T2DM heritability in SSA are preference for maternal aggregation, higher among first degree compared to second-degree relatives; early age-onset (ABCC8, Haptoglobin, KCNJ11, ACDC, ENPP1, TNF-α, and TCF7L2 were found to be associated with T2DM, with overlapping effect on specific cardiometabolic traits. Genome-wide studies identified ancestry-specific signals (AGMO-rs73284431, VT11A-rs17746147, and ZRANB3) and TCF7L2-rs7903146 as the only transferable genetic risk variants to SSA population. TCF7L2-rs7903146 polymorphism was investigated in multiple studies with consistent effects and low-moderate statistical heterogeneity. Effect sizes were modestly strong [odds ratio=6.17 (95% CI: 2.03-18.81), codominant model; 2.27 (95% CI: 1.50-3.44), additive model; 1.75 (95% CI: 1.18-2.59), recessive model]. Current evidence on the heritability and genetic markers of T2DM in SSA populations is limited and largely insufficient to reliably inform the genetic architecture of T2DM across SSA regions.
- Published
- 2020