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dc.contributor.authorKibirige, D
dc.contributor.authorSekitoleko, I
dc.contributor.authorLumu, W
dc.contributor.authorJones, AG
dc.contributor.authorHattersley, AT
dc.contributor.authorSmeeth, L
dc.contributor.authorNyirenda, MJ
dc.date.accessioned2023-02-24T14:31:57Z
dc.date.issued2022-02-09
dc.date.updated2023-02-24T12:22:16Z
dc.description.abstractAIMS/HYPOTHESIS: Apparent type 2 diabetes is increasingly reported in lean adult individuals in sub-Saharan Africa. However, studies undertaking robust clinical and metabolic characterisation of lean individuals with new-onset type 2 diabetes are limited in this population. This cross-sectional study aimed to perform a detailed clinical and metabolic characterisation of newly diagnosed adult patients with diabetes in Uganda, in order to compare features between lean and non-lean individuals. METHODS: Socio-demographic, clinical, biophysical and metabolic (including oral glucose tolerance test) data were collected on 568 adult patients with newly diagnosed diabetes. Participants were screened for islet autoantibodies to exclude those with autoimmune diabetes. The remaining participants (with type 2 diabetes) were then classified as lean (BMI <25 kg/m2) or non-lean (BMI ≥25 kg/m2), and their socio-demographic, clinical, biophysical and metabolic characteristics were compared. RESULTS: Thirty-four participants (6.4%) were excluded from analyses because they were positive for pancreatic autoantibodies, and a further 34 participants because they had incomplete data. For the remaining 500 participants, the median (IQR) age, BMI and HbA1c were 48 years (39-58), 27.5 kg/m2 (23.6-31.4) and 90 mmol/mol (61-113) (10.3% [7.7-12.5]), respectively, with a female predominance (approximately 57%). Of the 500 participants, 160 (32%) and 340 (68%) were lean and non-lean, respectively. Compared with non-lean participants, lean participants were mainly male (60.6% vs 35.3%, p<0.001) and had lower visceral adiposity level (5 [4-7] vs 11 [9-13], p<0.001) and features of the metabolic syndrome (uric acid, 246.5 [205.0-290.6] vs 289 [234-347] μmol/l, p<0.001; leptin, 660.9 [174.5-1993.1] vs 3988.0 [1336.0-6595.0] pg/ml, p<0.001). In addition, they displayed markedly reduced markers of beta cell function (oral insulinogenic index 0.8 [0.3-2.5] vs 1.6 [0.6-4.6] pmol/mmol; 120 min serum C-peptide 0.70 [0.33-1.36] vs 1.02 [0.60-1.66] nmol/l, p<0.001). CONCLUSIONS/INTERPRETATION: Approximately one-third of participants with incident adult-onset non-autoimmune diabetes had BMI <25 kg/m2. Diabetes in these lean individuals was more common in men, and predominantly associated with reduced pancreatic secretory function rather than insulin resistance. The underlying pathological mechanisms are unclear, but this is likely to have important management implications.en_GB
dc.description.sponsorshipNational Institute for Health Research (NIHR)en_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.description.sponsorshipDepartment for International Development
dc.format.extent675-683
dc.identifier.citationVol. 65, No. 4, pp. 675-683en_GB
dc.identifier.doihttps://doi.org/10.1007/s00125-021-05644-8
dc.identifier.grantnumber17/63/131en_GB
dc.identifier.grantnumberCS2015-15-018en_GB
dc.identifier.grantnumberMC_UP_1204/16en_GB
dc.identifier.grantnumber098395/Z/12/Zen_GB
dc.identifier.urihttp://hdl.handle.net/10871/132541
dc.identifierORCID: 0000-0002-0883-7599 (Jones, Angus G)
dc.identifierORCID: 0000-0001-5620-473X (Hattersley, Andrew T)
dc.language.isoenen_GB
dc.publisherSpringeren_GB
dc.rights© The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.en_GB
dc.subjectBeta cell dysfunctionen_GB
dc.subjectLean non-autoimmune diabetesen_GB
dc.subjectNewly diagnosed diabetes sub-Saharan Africaen_GB
dc.subjectType 2 diabetesen_GB
dc.subjectUgandaen_GB
dc.titleUnderstanding the pathogenesis of lean non-autoimmune diabetes in an African population with newly diagnosed diabetesen_GB
dc.typeArticleen_GB
dc.date.available2023-02-24T14:31:57Z
dc.identifier.issn0012-186X
exeter.place-of-publicationGermany
dc.descriptionThis is the final version. Available from Springer via the DOI in this record. en_GB
dc.identifier.eissn1432-0428
dc.identifier.journalDiabetologiaen_GB
dc.relation.ispartofDiabetologia, 65(4)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2021-11-12
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-02-09
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2023-02-24T14:26:41Z
refterms.versionFCDVoR
refterms.dateFOA2023-02-24T14:32:01Z
refterms.panelAen_GB
refterms.dateFirstOnline2022-02-09


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© The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Except where otherwise noted, this item's licence is described as © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.