Fasting Glucose Variation Predicts Microvascular Risk in ACCORD and VADT

J Clin Endocrinol Metab. 2021 Mar 25;106(4):1150-1162. doi: 10.1210/clinem/dgaa941.

Abstract

Aims: The association of glycemic variability with microvascular disease complications in type 2 diabetes (T2D) has been under-studied and remains unclear. We investigated this relationship using both Action to Control Cardiovascular Risk in Diabetes (ACCORD) and the Veteran Affairs Diabetes Trial (VADT).

Methods: In ACCORD, fasting plasma glucose (FPG) was measured 1 to 3 times/year for up to 84 months in 10 251 individuals. In the VADT, FPG was measured every 3 months for up to 87 months in 1791 individuals. Variability measures included coefficient of variation (CV) and average real variability (ARV) for fasting glucose. The primary composite outcome was time to either severe nephropathy or retinopathy event and secondary outcomes included each outcome individually. To assess the association, we considered variability measures as time-dependent covariates in Cox proportional hazard models. We conducted a meta-analysis across the 2 trials to estimate the risk of fasting glucose variability as well as to assess the heterogenous effects of FPG variability across treatment arms.

Results: In both ACCORD and the VADT, the CV and ARV of FPG were associated with development of future microvascular outcomes even after adjusting for other risk factors, including measures of average glycemic control (ie, cumulative average of HbA1c). Meta-analyses of these 2 trials confirmed these findings and indicated FPG variation may be more harmful in those with less intensive glucose control.

Conclusions: This post hoc analysis indicates that variability of FPG plays a role in, and/or is an independent and readily available marker of, development of microvascular complications in T2D.

Trial registration: ClinicalTrials.gov NCT00032487 NCT00000620.

Keywords: glycemic control; interaction; long-term glycemic variability; microvascular complications; type 2 diabetes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Aged
  • Blood Glucose / metabolism*
  • Cohort Studies
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / diagnosis*
  • Diabetes Mellitus, Type 2 / therapy
  • Diabetic Angiopathies / blood
  • Diabetic Angiopathies / diagnosis*
  • Diabetic Angiopathies / etiology
  • Diabetic Angiopathies / prevention & control
  • Fasting / blood
  • Female
  • Glycemic Control / methods
  • Heart Disease Risk Factors
  • Humans
  • Male
  • Microvascular Rarefaction / blood
  • Microvascular Rarefaction / diagnosis
  • Microvascular Rarefaction / etiology
  • Middle Aged
  • Prognosis
  • Randomized Controlled Trials as Topic
  • Treatment Outcome
  • United States
  • Veterans

Substances

  • Blood Glucose

Associated data

  • ClinicalTrials.gov/NCT00032487
  • ClinicalTrials.gov/NCT00000620