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The biological variation of insulin resistance markers: data from the European Biological Variation Study (EuBIVAS)

Authors
  • Carobene, Anna
  • Kilpatrick, Eric
  • Bartlett, William A.
  • Fernández Calle, Pilar
  • Coşkun, Abdurrahman
  • Díaz-Garzón, Jorge
  • Jonker, Niels
  • Locatelli, Massimo
  • Sandberg, Sverre
  • Aarsand, Aasne K.
Type
Published Article
Journal
Clinical Chemistry and Laboratory Medicine (CCLM)
Publisher
Walter de Gruyter GmbH
Publication Date
Jul 12, 2024
Volume
63
Issue
1
Pages
110–117
Identifiers
DOI: 10.1515/cclm-2024-0672
PMID: 38987271
Source
De Gruyter
Keywords
License
Yellow

Abstract

Objectives An insulin resistant state is characteristic of patients with type 2 diabetes, polycystic ovary syndrome, and metabolic syndrome. Identification of insulin resistance (IR) is most readily achievable using formulae combining plasma insulin and glucose results. In this study, we have used data from the European Biological Variation Study (EuBIVAS) to examine the biological variability (BV) of IR using the Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) and the Quantitative Insulin sensitivity Check Index (QUICKI). Methods Ninety EuBIVAS non-diabetic subjects (52F, 38M) from five countries had fasting HOMA-IR and QUICKI calculated from plasma glucose and insulin samples collected concurrently on 10 weekly occasions. The within-subject (CVI) and between-subject (CVG) BV estimates with 95 % CIs were obtained by CV-ANOVA after analysis of trends, variance homogeneity and outlier removal. Results The CVI of HOMA-IR was 26.7 % (95 % CI 25.5–28.3), driven largely by variability in plasma insulin and the CVI for QUICKI was 4.1 % (95 % CI 3.9–4.3), reflecting this formula’s logarithmic transformation of glucose and insulin values. No differences in values or BV components were observed between subgroups of men or women below and above 50 years. Conclusions The EuBIVAS, by utilising a rigorous experimental protocol, has produced robust BV estimates for two of the most commonly used markers of insulin resistance in non-diabetic subjects. This has shown that HOMA-IR, in particular, is highly variable in the same individual which limits the value of single measurements.

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