Key result
Longitudinal change in forced vital capacity was negatively associated with longitudinal change in HbA1c (β = -0.025, p = 0.026) and increased the risk of newly diagnosed type 2 diabetes.
Why the study?
Pulmonary impairment is frequent in diabetes, but the relationship between lung function and glycemic status in non-diabetic individuals was not well known.
Is pulmonary function decline associated with longitudinal changes in HbA1c and risk of incident type 2 diabetes in individuals without baseline diabetes, hypertension, or COPD?
Cohort (n=7,055)
Is pulmonary function decline associated with longitudinal changes in HbA1c and risk of incident type 2 diabetes in individuals without baseline diabetes, hypertension, or COPD?
Effect estimate: β = -0.025
p-value: p=0.026
Decline in forced vital capacity over time is associated with worsening glycemic control and an increased risk of incident type 2 diabetes in otherwise healthy individuals.
May link rising HbA1c to lung function decline before diabetes; hypothesis-generating and requires prospective confirmation.
Pulmonary damage and function impairment were frequently noted in patients with diabetes mellitus (DM). However, the relationship between lung function and glycemic status in non-DM subjects was not well-known. Here, we evaluated the association of longitudinal changes of lung function parameters with longitudinal changes of glycated hemoglobin (HbA1c) in non-DM participants. The study enrolled participants without prior type 2 DM, hypertension, and chronic obstructive pulmonary disease (COPD) from the Taiwan Biobank database. Laboratory profiles and pulmonary function parameters, including forced vital capacity (FVC) and forced expiratory volume in 1 s (FEV1), were examined at baseline and follow-up. Finally, 7055 participants were selected in this study. During a mean 3.9-year follow-up, FVC and FEV1 were significantly decreased over time (both p < 0.001). In the multivariable analysis, the baseline (unstandardized coefficient β = −0.032, p < 0.001) and longitudinal change (unstandardized coefficient β = −0.025, p = 0.026) of FVC were negatively associated with the baseline and longitudinal change of HbA1c, respectively. Additionally, the longitudinal change of FVC was negatively associated with the risk of newly diagnosed type 2 DM (p = 0.018). During a mean 3.9-year follow-up, our present study, including participants without type 2 DM, hypertension, and COPD, demonstrated that the baseline and longitudinal change of FVC were negatively and respectively correlated with the baseline and longitudinal change of HbA1c. Furthermore, compared to those without new-onset DM, participants with new-onset DM had a more pronounced decline of FVC over time.
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Lee et al. (2021) conducted a cohort in Without diabetes mellitus (n=7,055). Longitudinal change of forced vital capacity (FVC) was evaluated on Longitudinal change of HbA1c (β = -0.025, p=0.026). Longitudinal change in forced vital capacity was negatively associated with longitudinal change in HbA1c (β = -0.025, p = 0.026) and increased the risk of newly diagnosed type 2 diabetes.
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