Glycemic exposure is associated with reduced pulmonary function in type 2 diabetes - The Fremantle diabetes study

被引:227
作者
Davis, WA
Knuiman, M
Kendall, P
Grange, V
Davis, TME
机构
[1] Univ Western Australia, Fremantle Hosp, Sch Med & Pharmacol, Fremantle, WA 6959, Australia
[2] Univ Western Australia, Sch Populat Hlth, Perth, WA 6009, Australia
[3] Fremantle Hosp, Dept Resp Med, Fremantle, Australia
关键词
D O I
10.2337/diacare.27.3.752
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE- To examine prospectively the relationship between diabetes, glycemic control, and spirometric measures. RESEARCH DESIGN AND METHODS- From a community-based cohort, 495 Europid (i.e., of European descent) patients with type 2 diabetes who had no history of pulmonary disease underwent baseline spirometry between 1993 and 1994. A subset of 125 patients was restudied a mean of 7.0 years later. The main outcome measures included forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1), vital capacity (VC), and peak expiratory flow (PEF) corrected for body temperature, air pressure, and water saturation and were expressed either in absolute terms or as percentage-predicted value for age, sex, and height. RESULTS- Mean percentage-predicted values of each spirometric measure were decreased > 10% in the whole cohort at baseline and absolute measures continued to decline at an annual rate of 68, 71, and 84 ml/year and 17 l/min for FVC, FEV1, VC, and PEF, respectively, in the 125 prospectively studied patients. Declining lung function measures were consistently predicted by poor glycemic control in the form of a higher updated mean HbA(1c), follow-up HbA(1c), or follow-up fasting plasma glucose. In a Cox proportional hazards model, decreased FEV1 percentage-predicted value was an independent predictor of all-cause mortality. CONCLUSIONS- Reduced lung volumes and airflow limitation are likely to be chronic complications of type 2 diabetes, the severity of which relates to glycemic exposure. Airflow limitation is a predictor of death in type 2 diabetes after adjusting for other recognized risk factors.
引用
收藏
页码:752 / 757
页数:6
相关论文
共 37 条
[1]  
[Anonymous], 1995, AM J RESP CRIT CARE, V152, P1107
[2]   THE EFFECT OF PULMONARY IMPAIRMENT ON ALL-CAUSE MORTALITY IN A NATIONAL COHORT [J].
BANG, KM ;
GERGEN, PJ ;
KRAMER, R ;
COHEN, B .
CHEST, 1993, 103 (02) :536-540
[3]   NIDDM, impaired glucose tolerance, and pulmonary function in older adults - The Rancho Bernardo Study [J].
BarrettConnor, E ;
Frette, C .
DIABETES CARE, 1996, 19 (12) :1441-1444
[4]   IMPAIRED PULMONARY-FUNCTION AS A RISK FACTOR FOR MORTALITY [J].
BEATY, TH ;
COHEN, BH ;
NEWILL, CA ;
MENKES, HA ;
DIAMOND, EL ;
CHEN, CJ .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1982, 116 (01) :102-113
[5]  
Belda J, 1997, Arch Bronconeumol, V33, P488
[6]   Glycemic control in older subjects with type 2 diabetes mellitus in the Fremantle diabetes study [J].
Bruce, DG ;
Davis, WA ;
Davis, TME .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2000, 48 (11) :1449-1453
[7]   Autoantibodies to glutamic acid decarboxylase in diabetic patients from a multi-ethnic Australian community: the Fremantle Diabetes Study [J].
Davis, TME ;
Zimmet, P ;
Davis, WA ;
Bruce, DG ;
Fida, S ;
Mackay, IR .
DIABETIC MEDICINE, 2000, 17 (09) :667-674
[8]   Reduced pulmonary function and its associations in type 2 diabetes: the Fremantle Diabetes Study [J].
Davis, TME ;
Knuiman, M ;
Kendall, P ;
Vu, H ;
Davis, WA .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2000, 50 (02) :153-159
[9]   DISTRIBUTION OF FORCED EXPIRATORY VOLUME IN ONE 2ND AND FORCED VITAL CAPACITY IN HEALTHY, WHITE, ADULT NEVER-SMOKERS IN 6 UNITED-STATES CITIES [J].
DOCKERY, DW ;
WARE, JH ;
FERRIS, BG ;
GLICKSBERG, DS ;
FAY, ME ;
SPIRO, A ;
SPEIZER, FE .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1985, 131 (04) :511-520
[10]   BREATHLESSNESS, CHRONIC-BRONCHITIS AND REDUCED PULMONARY-FUNCTION AS PREDICTORS OF CARDIOVASCULAR-DISEASE MORTALITY AMONG MEN IN ENGLAND, SCOTLAND AND THE UNITED-STATES [J].
EBIKRYSTON, KL ;
HAWTHORNE, VM ;
ROSE, G ;
SHIPLEY, MJ ;
GILLIS, CR ;
HOLE, DJ ;
CARMEN, W ;
ESHLEMAN, S ;
HIGGINS, MW .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1989, 18 (01) :84-88