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Associations of the HOMA2‐%B and HOMA2‐IR with progression to diabetes and glycaemic deterioration in young and middle‐aged Chinese

AIMS: Insulin deficiency (ID) and resistance (IR) contribute to progression from normal glucose tolerance to diabetes to insulin requirement although their relative contributions in young‐onset diabetes is unknown. METHODS: We examined the associations of HOMA2 using fasting plasma glucose and C‐pep...

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Detalles Bibliográficos
Autores principales: Fan, Baoqi, Wu, Hongjiang, Shi, Mai, Yang, Aimin, Lau, Eric S. H., Tam, Claudia H. T., Mao, Dandan, Lim, Cadmon K. P., Kong, Alice P. S., Ma, Ronald C. W., Chow, Elaine, Luk, Andrea O. Y., Chan, Juliana C. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542522/
https://www.ncbi.nlm.nih.gov/pubmed/35174618
http://dx.doi.org/10.1002/dmrr.3525
Descripción
Sumario:AIMS: Insulin deficiency (ID) and resistance (IR) contribute to progression from normal glucose tolerance to diabetes to insulin requirement although their relative contributions in young‐onset diabetes is unknown. METHODS: We examined the associations of HOMA2 using fasting plasma glucose and C‐peptide in Chinese aged 20–50 years with (1) progression to type 2 diabetes (T2D) in participants without diabetes in a community‐based cohort (1998–2013) and (2) glycaemic deterioration in patients with T2D in a clinic‐based cohort (1995–2014). We defined ID as HOMA2‐%B below median and insulin IR as HOMA2‐IR above median. RESULTS: During 10‐year follow‐up, 62 (17.9%) of 347 community‐dwelling participants progressed to T2D. After 8.6 years, 291 (48.1%) of 609 patients with T2D had glycaemic deterioration. At baseline, progressors for T2D had higher HOMA2‐IR, while in patients with T2D, progressors for glycaemic deterioration had higher HOMA2‐IR and lower HOMA2‐%B than non‐progressors. The non‐ID/IR group and the ID/IR group had an adjusted odds ratios of 2.47 (95% CI: 1.28, 4.94) and 5.36 (2.26, 12.79), respectively, for incident T2D versus the ID/non‐IR group. In patients with T2D, 50% of the ID/IR group required insulin at 6.7 years versus around 11 years in the non‐ID/IR or ID/non‐IR, and more than 15 years in the non‐ID/non‐IR group. Compared with the latter group, the adjusted hazard ratios were 2.74 (1.80, 4.16) in the ID/non‐IR, 2.73 (1.78, 4.19) in the non‐ID/IR and 4.46 (2.87, 6.91) in the ID/IR group (p‐interaction = 0.049). CONCLUSIONS: In young Chinese adults, IR and ID contributed to progression to T2D and glycaemic deterioration.