Type 1 diabetes in Africa: an immunogenetic study in the Amhara of North-West Ethiopia.

Journal: Diabetologia

Volume: 63

Issue: 10

Year of Publication: 2021

Affiliated Institutions:  Department of Internal Medicine, Gondar University Hospital, Gondar, Ethiopia. Department of Pediatrics and Child Health, School of Medicine, University of Gondar, Gondar, Ethiopia. Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA. Blizard Institute, Queen Mary University of London, London, UK. Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Main Line Health System, Wynnewood, PA, USA. Severn Postgraduate School of Primary Care, Health Education England, Bristol, UK. Avon and Wiltshire Mental Health Partnership NHS Trust, Clevedon, UK. Diabetes and Metabolism, Translational Health Sciences, University of Bristol, Southmead Hospital, Bristol, UK. MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton, UK. Centre for Public Health, Institute of Clinical Science, Queen's University Belfast, Grosvenor Road, Belfast, BT BA, UK. e.trimble@qub.ac.uk.

Abstract summary 

We aimed to characterise the immunogenic background of insulin-dependent diabetes in a resource-poor rural African community. The study was initiated because reports of low autoantibody prevalence and phenotypic differences from European-origin cases with type 1 diabetes have raised doubts as to the role of autoimmunity in this and similar populations.A study of consecutive, unselected cases of recently diagnosed, insulin-dependent diabetes (n = 236, ≤35 years) and control participants (n = 200) was carried out in the ethnic Amhara of rural North-West Ethiopia. We assessed their demographic and socioeconomic characteristics, and measured non-fasting C-peptide, diabetes-associated autoantibodies and HLA-DRB1 alleles. Leveraging genome-wide genotyping, we performed both a principal component analysis and, given the relatively modest sample size, a provisional genome-wide association study. Type 1 diabetes genetic risk scores were calculated to compare their genetic background with known European type 1 diabetes determinants.Patients presented with stunted growth and low BMI, and were insulin sensitive; only 15.3% had diabetes onset at ≤15 years. C-peptide levels were low but not absent. With clinical diabetes onset at ≤15, 16-25 and 26-35 years, 86.1%, 59.7% and 50.0% were autoantibody positive, respectively. Most had autoantibodies to GAD (GADA) as a single antibody; the prevalence of positivity for autoantibodies to IA-2 (IA-2A) and ZnT8 (ZnT8A) was low in all age groups. Principal component analysis showed that the Amhara genomes were distinct from modern European and other African genomes. HLA-DRB1*03:01 (p = 0.0014) and HLA-DRB1*04 (p = 0.0001) were positively associated with this form of diabetes, while HLA-DRB1*15 was protective (p < 0.0001). The mean type 1 diabetes genetic risk score (derived from European data) was higher in patients than control participants (p = 1.60 × 10). Interestingly, despite the modest sample size, autoantibody-positive patients revealed evidence of association with SNPs in the well-characterised MHC region, already known to explain half of type 1 diabetes heritability in Europeans.The majority of patients with insulin-dependent diabetes in rural North-West Ethiopia have the immunogenetic characteristics of autoimmune type 1 diabetes. Phenotypic differences between type 1 diabetes in rural North-West Ethiopia and the industrialised world remain unexplained.

Authors & Co-authors:  Balcha Shitaye A SA Demisse Abayneh G AG Mishra Rajashree R Vartak Tanwi T Cousminer Diana L DL Hodge Kenyaita M KM Voight Benjamin F BF Lorenz Kim K Schwartz Stanley S Jerram Samuel T ST Gamper Arla A Holmes Alice A Wilson Hannah F HF Williams Alistair J K AJK Grant Struan F A SFA Leslie R David RD Phillips David I W DIW Trimble Elisabeth R ER

Study Outcome 

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Statistics
Citations :  Balcha SA, Phillips DIW, Trimble ER. Type 1 diabetes in a resource-poor setting: malnutrition related, malnutrition modified, or just diabetes? Curr Diab Rep. 2018;18:47. doi: 10.1007/s11892-018-1003-7.
Authors :  18
Identifiers
Doi : 10.1007/s00125-020-05229-x
SSN : 1432-0428
Study Population
Male,Female
Mesh Terms
Adolescent
Other Terms
Africa;Autoantibodies;Ethiopia;Genomes;HLA;Rural;Type 1 diabetes
Study Design
Case Control Trial,Cross Sectional Study
Study Approach
Country of Study
Ethiopia
Publication Country
Germany