Identification of a subgroup of black South Africans with type 1 diabetes who are older at diagnosis but have lower levels of glutamic acid decarboxylase and islet antigen 2 autoantibodies

dc.contributor.authorPadoa, Carolyn J.
dc.contributor.authorRheeder, Paul
dc.contributor.authorPirie, Fraser J.
dc.contributor.authorMotala, Ayesha A.
dc.contributor.authorVan Dyk, Jacobus C.
dc.contributor.authorCrowther, Nigel J.
dc.date.accessioned2020-03-31T11:35:27Z
dc.date.issued2020-12
dc.description.abstractAIMS : To compare the age at diagnosis and prevalence of islet autoantibody [glutamic acid decarboxylase (65 kDa) 65 and islet antigen 2] positivity in black and white participants with type 1 diabetes in South Africa, and to analyse the relationship between age at diagnosis and the presence of autoantibodies. METHODS : Participants were recruited from diabetes outpatient departments and autoantibodies to glutamic acid decarboxylase (65 kDa) and islet antigen 2 were measured by enzyme‐linked immunosorbent assay. RESULTS : We recruited 472 (353 black and 119 white) participants with type 1 diabetes. Age at diagnosis of diabetes was later in black (19.7 ± 10.5) than in white participants (12.7 ± 10.8 years; P < 0.001) with a median (interquartile range) disease duration of 5.0 (2.0–10.0) and 8.5 (4.0–20.0) years (P < 0.001), respectively. An older age at diagnosis (≥ 21 years) was more frequent in black (152 of 340, 45%) than in white participants (24 of 116, 21%; P < 0.001). The prevalence of islet antigen 2 autoantibodies was 19% (66/352) in black and 41% in white participants (48/118; P < 0.001). There was no significant difference in glutamic acid decarboxylase (65 kDa) autoantibody positivity between black (212/353, 60%) and white participants (77/117, 66%; P = 0.269). In black, but not white, participants the prevalence of both glutamic acid decarboxylase (65 kDa) and islet antigen 2 autoantibody positivity was significantly lower in participants diagnosed at age ≥ 21 years (P < 0.001 for both comparisons). CONCLUSIONS : The older age at diagnosis, lower prevalence of islet antigen 2 autoantibodies and a distinct subgroup of participants with type 1 diabetes with age at diagnosis of > 20 years in the black compared to white population suggest a difference in the immunological aetiology of type 1 diabetes in these two population groups.en_ZA
dc.description.departmentInternal Medicineen_ZA
dc.description.embargo2020-12-06
dc.description.librarianhj2020en_ZA
dc.description.sponsorshipThe South African Medical Research Council and the National Health Laboratory Service Research Trust (94472).en_ZA
dc.description.urihttps://onlinelibrary.wiley.com/journal/14645491en_ZA
dc.identifier.citationPadoa, C.J., Rheeder, P., Pirie, F.J. et al. 2020, 'Identification of a subgroup of black South Africans with type 1 diabetes who are older at diagnosis but have lower levels of glutamic acid decarboxylase and islet antigen 2 autoantibodies', Diabetic Medicine, vol. 37, no. 12, pp. 2067-2074.en_ZA
dc.identifier.issn0742-3071 (print)
dc.identifier.issn1464-5491 (online)
dc.identifier.other10.1111/dme.14204
dc.identifier.urihttp://hdl.handle.net/2263/73886
dc.language.isoenen_ZA
dc.publisherWileyen_ZA
dc.rights© 2019 Diabetes UK. This is the pre-peer reviewed version of the following article : 'Identification of a subgroup of black South Africans with type 1 diabetes who are older at diagnosis but have lower levels of glutamic acid decarboxylase and islet antigen 2 autoantibodies', Diabetic Medicine, vol. 37, no. 12, pp. 2067-2074, 2020, doi : 10.1111/dme.14204. The definite version is available at : https://onlinelibrary.wiley.com/journal/14645491.en_ZA
dc.subjectAutoantibodiesen_ZA
dc.subjectBlack populationen_ZA
dc.subjectGAD65en_ZA
dc.subjectIA-2en_ZA
dc.subjectOlder age at diagnosisen_ZA
dc.subjectSouth Africa (SA)en_ZA
dc.subjectType 1 diabetesen_ZA
dc.titleIdentification of a subgroup of black South Africans with type 1 diabetes who are older at diagnosis but have lower levels of glutamic acid decarboxylase and islet antigen 2 autoantibodiesen_ZA
dc.typePostprint Articleen_ZA

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