TY - JOUR
T1 - Reduced pulmonary function and its associations in type 2 diabetes: the Fremantle Diabetes Study
AU - Davis, Timothy
AU - Knuiman, Matthew
AU - Kendall, Peter
AU - Vu, H.
AU - Davis, W.A.
PY - 2000
Y1 - 2000
N2 - To determine whether diabetes is associated with reduced lung function, we studied 421 Angle-Celt/European subjects, representing 20.5% of all patients with type 2 diabetes identified in an urban Australian catchment area of 120 097 people. In addition to collection of detailed demographic and diabetes-specific data, spirometry was performed and forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1), vital capacity (VC) and peak expiratory flow (PEF) measured. When expressed as a percentage of those predicted (%pred) for age, sex and height, the means of all spirometric measures were reduced by greater than or equal to 9.5%. After controlling for smoking, age and gender in a linear regression model, HbA(1c) was not associated with any measure of lung function (P>0.13) but diabetes duration was significantly associated with FEV1(%pred) and PEF%pred (P less than or equal to 0.04) and had borderline associations with FVC%pred and VC%pred (P less than or equal to 0.064). In separate analyses controlling for smoking alone, age, body mass index (BMI), coronary heart disease (CHD) and retinopathy were independently and inversely associated with FVC%pred, FEV1%pred and VC%pred (P <0.05). In sub-group analyses, these three spirometric measures were associated with BMI, CHD and diabetes duration in males, and age and BMI in females. Pulmonary function is reduced in type 2 diabetes. Diabetes duration seems a more important influence than glycaemic control, but obesity and vascular disease may also contribute. (C) 2000 Elsevier Science Ireland Lid. All rights reserved.
AB - To determine whether diabetes is associated with reduced lung function, we studied 421 Angle-Celt/European subjects, representing 20.5% of all patients with type 2 diabetes identified in an urban Australian catchment area of 120 097 people. In addition to collection of detailed demographic and diabetes-specific data, spirometry was performed and forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1), vital capacity (VC) and peak expiratory flow (PEF) measured. When expressed as a percentage of those predicted (%pred) for age, sex and height, the means of all spirometric measures were reduced by greater than or equal to 9.5%. After controlling for smoking, age and gender in a linear regression model, HbA(1c) was not associated with any measure of lung function (P>0.13) but diabetes duration was significantly associated with FEV1(%pred) and PEF%pred (P less than or equal to 0.04) and had borderline associations with FVC%pred and VC%pred (P less than or equal to 0.064). In separate analyses controlling for smoking alone, age, body mass index (BMI), coronary heart disease (CHD) and retinopathy were independently and inversely associated with FVC%pred, FEV1%pred and VC%pred (P <0.05). In sub-group analyses, these three spirometric measures were associated with BMI, CHD and diabetes duration in males, and age and BMI in females. Pulmonary function is reduced in type 2 diabetes. Diabetes duration seems a more important influence than glycaemic control, but obesity and vascular disease may also contribute. (C) 2000 Elsevier Science Ireland Lid. All rights reserved.
U2 - 10.1016/S0168-8227(00)00166-2
DO - 10.1016/S0168-8227(00)00166-2
M3 - Article
SN - 0168-8227
VL - 50
SP - 153
EP - 159
JO - Diabetes Research and Clinical Practice
JF - Diabetes Research and Clinical Practice
IS - 2
ER -