학술논문

Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function
Document Type
article
Source
British Journal Of Nutrition. 120(10)
Subject
Biomedical and Clinical Sciences
Nutrition and Dietetics
Complementary and Integrative Health
Aging
Clinical Research
Adult
Aged
Black People
Cross-Sectional Studies
Female
Forced Expiratory Volume
Genome
Human
Heart
Heart Diseases
Humans
Lung
Lung Diseases
Male
Middle Aged
Molecular Epidemiology
Prospective Studies
Regression Analysis
Respiratory Function Tests
Smoking
Vital Capacity
Vitamin D
White People
1
25(OH)D 25-hydroxyvitamin D
AA African ancestry
AGES Age
ARIC Atherosclerosis Risk in Communities Study
Aging
CARDIA Coronary Artery Risk Development in Young Adults Study
CHARGE Cohorts for Heart and Aging Research in Genomic Epidemiology
CHS Cardiovascular Health Study
COPD chronic obstructive pulmonary disease
EA European ancestry
Environment
FEV1 forced expiratory volume in the 1st second
FHS (Gen3) Framingham Heart Study – Generation 3 Cohort
FHS (Offspring) Framingham Heart Study –Offspring Cohort
FVC forced vital capacity
Gene
HABC Health
Iceland
MESA Multi-Ethnic Study of Atherosclerosis
PFT pulmonary function test
RIA radioimmunoassay
Susceptibility Study − Reykjavik
and Body Composition Study
25-(OH)2D 1
25-dihydroxyvitamin D
African Americans
Forced expiratory volume
Respiratory function tests
Vital capacity
Whites
Animal Production
Food Sciences
Nutrition & Dietetics
Animal production
Food sciences
Nutrition and dietetics
Language
Abstract
The role that vitamin D plays in pulmonary function remains uncertain. Epidemiological studies reported mixed findings for serum 25-hydroxyvitamin D (25(OH)D)-pulmonary function association. We conducted the largest cross-sectional meta-analysis of the 25(OH)D-pulmonary function association to date, based on nine European ancestry (EA) cohorts (n 22 838) and five African ancestry (AA) cohorts (n 4290) in the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. Data were analysed using linear models by cohort and ancestry. Effect modification by smoking status (current/former/never) was tested. Results were combined using fixed-effects meta-analysis. Mean serum 25(OH)D was 68 (sd 29) nmol/l for EA and 49 (sd 21) nmol/l for AA. For each 1 nmol/l higher 25(OH)D, forced expiratory volume in the 1st second (FEV1) was higher by 1·1 ml in EA (95 % CI 0·9, 1·3; P