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January 10, 2026Diabetes Care2 citations

Metabolic Factors Modulating the Connection Between Diabetes and Pulmonary Alterations

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MMMaurizio Di MarcoKBKálmán BódisZLZengbin Li

Key Result

Increased insulin resistance and higher daily insulin doses are associated with lower FEV1 and FVC in individuals with diabetes, indicating potential underlying pathogenic mechanisms.

Key Points

  • This research aims to investigate how glucose and insulin metabolism affect lung function in individuals with Type 1 and Type 2 diabetes compared to those with normal glucose tolerance.
  • Analyzed spirometry data from the German Diabetes Study, including 426 individuals with Type 1 diabetes and 482 with Type 2 diabetes.
  • Utilized generalized linear models to assess associations between metabolic measures and lung function, adjusting for confounders.
  • Conducted Mendelian randomization analyses using data from independent cohorts to establish causality.
  • Higher insulin sensitivity (M value) and insulin clearance were associated with increased FEV1 and FVC.
  • Type 2 diabetes individuals exhibited lower FEV1 and FVC compared to Type 1 diabetes and control groups, linked to reduced insulin sensitivity.
  • FEV1 negatively correlated with daily insulin doses in Type 1 diabetes and various diabetes classifications, pointing to insulin resistance as a potential risk factor.

Structured PICO

Is insulin resistance and diabetes associated with reduced pulmonary function?

P
Population
1,152 participants in the German Diabetes Study (426 with type 1 diabetes, 482 with type 2 diabetes, 244 with normal glucose tolerance) and independent cohorts for Mendelian randomization (n=37,037 for HOMA-IR, n=321,047 for pulmonary function).
C
Comparator
Normal glucose tolerance (CON)
O
Outcome
Forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC)surrogate

Insulin resistance and hyperinsulinemia are likely causal mechanisms underlying reduced pulmonary function in patients with diabetes.

Abstract

OBJECTIVE Type 1 and 2 diabetes have been variably associated with reduced forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC), but mechanisms remain unclear. This study examined the role of glucose and insulin metabolism for pulmonary function across diabetes (sub)types and normal glucose tolerance as the control (CON) in the German Diabetes Study (GDS) and assessed causality by Mendelian randomization (MR) analyses in independent cohorts. RESEARCH DESIGN AND METHODS In GDS, 426 spirometry measurements of participants with type 1 diabetes, 482 of participants with type 2 diabetes, and 244 of CON were cross-sectionally analyzed after phenotyping, including Botnia clamps for insulin sensitivity (M value), secretion, and clearance. Associations between metabolic measures and lung function were assessed using generalized linear models, adjusting for confounders. MR analysis used data from the MAGIC (Meta-Analyses of Glucose and Insulin-Related Traits Consortium) consortium (HOMA-insulin resistance IR, n = 37,037) and the UK Household Longitudinal Study (pulmonary function, n = 321,047). RESULTS In GDS, higher M value (all β 0.18, P 0.0001) and insulin clearance (all β = 0.05, P 0.050) were associated with higher FEV1 and FVC. Compared with type 1 diabetes and CON, type 2 diabetes had lower FEV1 and FVC, which associated with M value (all β 0.17, P 0.050). FEV1 was associated with daily insulin doses in type 1 diabetes (β = −0.21, P = 0.0006). FEV1 was associated with type 2 diabetes (β = −0.19, P = 0.0052), severe insulin resistant (β =−0.27, P = 0.039), and mild age-related diabetes (β = −0.23, P = 0.0033). MR supported a causal association between HOMA-IR and lower FEV1 (β = −0.13, P = 0.0018). CONCLUSIONS Lower FEV1 and FVC in diabetes are linked to insulin resistance, impaired clearance, and higher insulin doses, all of which result in higher insulinemia and likely represent underlying pathogenic mechanisms.

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Cite This Study

Marco et al. (2025) studied this question. Increased insulin resistance and higher daily insulin doses are associated with lower FEV1 and FVC in individuals with diabetes, indicating potential underlying pathogenic mechanisms.

synapsesocial.com/papers/6963220a91e05aa366cb8742https://doi.org/10.2337/dc25-2334
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