Type 2 & other diabetes

Relationship of Plasma Apolipoprotein C-I Truncation With Risk of Diabetes in the Multi-Ethnic Study of Atherosclerosis and the Actos Now for the Prevention of Diabetes Study

Diabetes CarePublished Prospective cohort study

Authors' conclusion

Our results indicate that apoC-I truncation may contribute to changes in glucose levels, IR, and risk of diabetes.

Study context

Population
Nondiabetic participants in Multi-Ethnic Study of Atherosclerosis (MESA) and participants with prediabetes in ACT NOW4,742 MESA · Nondiabetic participants in MESA 4,742 · participants with prediabetes in ACT NOW 524
Exposure
Higher vs lower truncated-to-native apoC-I proteoform ratio, per SD
Outcome
Incident diabetes (FPG ≥7.0 mmol/L or hypoglycemic medication use in MESA; FPG ≥7.0 mmol/L or 2-h glucose ≥11.1 mmol/L on OGTT in ACT NOW)
Methodological detailstwo cohorts: MESA and ACT NOW, mass spectrometry immunoassay
  • Two cohorts: MESA and ACT NOW
  • Mass spectrometry immunoassay

Main finding

As reported in the abstract

Incident diabetes per SD higher C-I'/C-I

MESA: HR per SD (564 events; median follow-up 9 years)

0.87

95% CI 0.79, 0.95P = 0.0036

ACT NOW: per SD (59 events; median follow-up 2.5 years)

0.66

95% CI 0.48, 0.91P = 0.004

Observational data: associations, not effects.

Secondary outcomes

MESA: change in FPG and HOMA-IR with higher C-I'/C-I

FPG (smaller increase)
−0.5%; P < 0.0001
HOMA-IR (smaller increase)
−2.9%; P = 0.011
  • Follow-up adjusted for baseline

MESA: total apoC-I concentrations

Not associated with changes in FPG, HOMA-IR or incident diabetes

ACT NOW: change in OGTT AUCglucose and Matsuda insulin sensitivity index (ISI) with higher C-I'/C-I

AUCglucose (smaller increase)
−1.8%; P = 0.0052
ISI (greater increase)
7.2%; P = 0.0095

Original publication

Relationship of Plasma Apolipoprotein C-I Truncation With Risk of Diabetes in the Multi-Ethnic Study of Atherosclerosis and the Actos Now for the Prevention of Diabetes Study. Diabetes Care. Published 25 October 2024. doi:10.2337/dc24-1462

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