Early-onset diabetes in Africa: A mini-review of the current genetic profile
Samuel Mawuli AdadeyiD, Joy Afua Mensah, Kojo Sekyi AcquahiD, James AbugriiD, Richard Osei‐YeboahiD
Abstract
Early-onset diabetes is poorly diagnosed partly due to its heterogeneity and variable presentations. Although several genes have been associated with the disease, these genes are not well studied in Africa. We sought to identify the major neonatal, early childhood, juvenile, or early-onset diabetes genes in Africa; and evaluate the available molecular methods used for investigating these gene variants. A literature search was conducted on PubMed, Scopus, Africa-Wide Information, and Web of Science databases. The retrieved records were screened and analyzed to identify genetic variants associated with early-onset diabetes. Although 319 records were retrieved, 32 were considered for the current review. Most of these records (22/32) were from North Africa. The disease condition was genetically heterogenous with most cases possessing unique gene variants. We identified 22 genes associated with early-onset diabetes, 9 of which had variants (n=19) classified as pathogenic or likely pathogenic (PLP). Among the PLP variants, IER3IP1: p.(Leu78Pro) was the variant with the highest number of cases. There was limited data from West Africa, hence the contribution of genetic variability to early-onset diabetes in Africa could not be comprehensively evaluated. It is worth mentioning that most studies were focused on natural products as antidiabetics and only a few studies reported on the genetics of the disease. ABCC8 and KCNJ11 were implicated as major contributors to early-onset diabetes gene networks. Gene ontology analysis of the network associated ion channels, impaired glucose tolerance, and decreased insulin secretions to the disease. Our review highlights 9 genes from which PLP variants have been identified and can be considered for the development of an African diagnostic panel. There is a gap in early-onset diabetes genetic research from sub-Saharan Africa which is much needed to develop a comprehensive, efficient, and cost-effective genetic panel that will be useful in clinical practice on the continent and among the African diasporas.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 2
- FWCI
- 0.08
- Field percentile
- 13th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The rare DRB1*04-DQ8 haplotype is the main discriminative HLA class II genetic driver of Early-Onset Type 1 Diabetes in the Portuguese population
Íris Caramalho, Paula Matoso, … Carlos Penha‐Gonçalves·medRxiv·Jul 23, 2023
- Common Genetic Variants Modify Disease Risk and Clinical Presentation in Monogenic Diabetes
Jacques Murray Leech, Robin N. Beaumont, … Kashyap Amratlal Patel·Nature MetabolismPeer-reviewed·Sep 9, 2025
- Specific type 1 diabetes risk genes underpin age-at-diagnosis and indicate joint defects in immunity, beta-cell fragility and responses to viral infections in early-onset disease.
Jamie R. J. Inshaw, Antony J. Cutler, … John A. Todd·Diabetes CarePeer-reviewed·Sep 26, 2019
- Population-Scale, Genotype-First Characterization of Monogenic Diabetes in 374,973 Multi-Ancestry Individuals from the All of Us Research Program
Masashi Hasebe, Satoshi Yoshiji·medRxiv·Jun 22, 2026
- Precision medicine for developmental and epileptic encephalopathies in Africa: strategies for a resource-limited setting.
Alina Izabela Esterhuizen, Nicki Tiffin, … Gemma L. Carvill·Genetics in MedicinePeer-reviewed·Dec 8, 2022
- An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls
Sam Hodgson, Vi Bui, … Moneeza Kalhan Siddiqui·medRxiv·Sep 24, 2025