4.3 Article

β-cell dysfunction and insulin resistance in relation to pre-diabetes and diabetes among adults in north-western Tanzania: a cross-sectional study

Journal

TROPICAL MEDICINE & INTERNATIONAL HEALTH
Volume 26, Issue 4, Pages 435-443

Publisher

WILEY
DOI: 10.1111/tmi.13545

Keywords

beta-cell dysfunction; insulin resistance; pre-diabetes; diabetes; HIV

Funding

  1. Ministry of Foreign Affairs of Denmark [16-P01-TAN]
  2. MRC [MR/R010161/1] Funding Source: UKRI

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Studies in Africa show that beta-cell dysfunction appears to play a more significant role in diabetes compared to insulin resistance, with a higher risk of prediabetes and diabetes associated with beta-cell dysfunction, insulin resistance, and combined dysfunction and resistance. Further cohort studies are needed to confirm these findings.
Objective Studies on phenotypes of diabetes in Africa are inconsistent. We assessed the role of beta-cell dysfunction and insulin resistance on pre-diabetes and diabetes. Methods We included 1890 participants with mean age of 40.6 (SD11.9) years in a cross-sectional study among male and female adults in Tanzania during 2016 to 2017. Data on C-reactive protein (CRP), alpha-acid glycoprotein (AGP), HIV, oral glucose tolerance test (OGTT), body composition and insulin were collected. Insulinogenic index and HOMA-IR were used to derive an overall marker of beta-cell dysfunction and insulin resistance which was categorised as follows: normal beta-cell function and insulin sensitivity, isolated beta-cell dysfunction, isolated insulin resistance, and combined beta-cell dysfunction and insulin resistance. Pre-diabetes and diabetes were defined as 2-hour OGTT glucose between 7.8-11.0 and >= 11.1 mmol/L, respectively. Multinomial regression assessed the association of beta-cell dysfunction and insulin resistance with outcome measures. Results beta-cell dysfunction, insulin resistance, and combined beta-cell dysfunction and insulin resistance were associated with higher pre-diabetes risk. Similarly, isolated beta-cell dysfunction (adjusted relative risk ratio (aRRR) 4.8 (95% confidence interval (CI) 2.5, 9.0), isolated insulin resistance (aRRR 3.2 (95% CI 1.5, 6.9), and combined beta-cell dysfunction and insulin resistance (aRRR 35.9 (95% CI 17.2, 75.2) were associated with higher diabetes risk. CRP, AGP and HIV were associated with higher diabetes risk, but fat mass was not. 31%, 10% and 33% of diabetes cases were attributed to beta-cell dysfunction, insulin resistance, and combined beta-cell dysfunction and insulin resistance, respectively. Conclusions beta-cell dysfunction seemed to explain most of diabetes cases compared to insulin resistance in this population. Cohort studies on evolution of diabetes in Africa are needed to confirm these results.

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