Longitudinal change in lung function and subsequent risks of cardiovascular events: evidence from four prospective cohort studies

被引:14
|
作者
Cheng, Yun-Jiu [1 ,2 ]
Chen, Zhen-Guang [3 ]
Li, Zhu-Yu [4 ]
Mei, Wei-Yi [1 ,2 ]
Bi, Wen-Tao [1 ,2 ]
Luo, Dong-Ling [5 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Cardiol, Guangzhou 510700, Peoples R China
[2] Sun Yat Sen Univ, NHC Key Lab Assisted Circulat, Guangzhou, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Thorac Surg, Guangzhou, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Guangzhou, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 8, Dept Cardiol, Shenzhen 518033, Peoples R China
基金
中国国家自然科学基金;
关键词
Lung function; Change; Cardiovascular events; Coronary heart disease; Heart failure; OBSTRUCTIVE PULMONARY-DISEASE; AIR-FLOW OBSTRUCTION; CORONARY-HEART-DISEASE; SUDDEN CARDIAC DEATH; ATHEROSCLEROSIS RISK; FUNCTION DECLINE; NATURAL-HISTORY; RAPID DECLINE; ASSOCIATION; OUTCOMES;
D O I
10.1186/s12916-021-02023-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Lung function is constantly changing over the life course. Although the relation of cross-sectional lung function measure and adverse outcomes has been reported, data on longitudinal change and subsequent cardiovascular (CV) events risks are scarce. Therefore, this study is to determine the association of longitudinal change in lung function and subsequent cardiovascular risks. Methods This study analyzed the data from four prospective cohorts. Subjects with at least two lung function tests were included. We calculated the rate of forced respiratory volume in 1 s (FEV1) and forced vital capacity (FVC) decline for each subject and categorized them into quartiles. The primary outcome was CV events, defined as a composite of coronary heart disease (CHD), chronic heart failure (CHF), stroke, and any CV death. Cox proportional hazards regression and restricted cubic spline models were applied. Results The final sample comprised 12,899 participants (mean age 48.58 years; 43.61% male). Following an average of 14.79 (10.69) years, 3950 CV events occurred. Compared with the highest FEV1 quartile (Q4), the multivariable HRs for the lowest (Q1), 2nd (Q2), and 3rd quartiles (Q3) were 1.33 (95%CI 1.19, 1.49), 1.30 (1.16, 1.46), and 1.07 (0.95, 1.21), respectively. Likewise, compared with the reference quartile (Q4), the group that experienced a faster decline in FVC had higher HRs for CV events (1.06 [95%CI 0.94-1.20] for Q3, 1.15 [1.02-1.30] for Q2, and 1.28 [1.14-1.44] for Q1). The association remained robust across a series of sensitivity analyses and nearly all subgroups but was more evident in subjects < 60 years. Conclusions We observed a monotonic increase in risks of CV events with a faster decline in FEV1 and FVC. These findings emphasize the value of periodic evaluation of lung function and open new opportunities for disease prevention.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Consumption of whole grains and refined grains and associated risk of cardiovascular disease events and all-cause mortality: a systematic review and dose-response meta-analysis of prospective cohort studies
    Hu, Huifang
    Zhao, Yang
    Feng, Yifei
    Yang, Xingjin
    Li, Yang
    Wu, Yuying
    Yuan, Lijun
    Zhang, Jinli
    Li, Tianze
    Huang, Hao
    Li, Xi
    Zhang, Ming
    Sun, Liang
    Hu, Dongsheng
    AMERICAN JOURNAL OF CLINICAL NUTRITION, 2023, 117 (01) : 149 - 159
  • [22] Association of weight change with cardiovascular events and all-cause mortality in obese participants with cardiovascular disease: a prospective cohort study
    Zhang, Jufen
    Schutte, Rudolph
    Pierscionek, Barbara
    HEART, 2025, : 454 - 461
  • [23] Cannabis use and psychosocial functioning: evidence from prospective longitudinal studies
    Meier, Madeline H.
    CURRENT OPINION IN PSYCHOLOGY, 2021, 38 : 19 - 24
  • [24] Whole Grain Intake and Mortality From All Causes, Cardiovascular Disease, and Cancer A Meta-Analysis of Prospective Cohort Studies
    Zong, Geng
    Gao, Alisa
    Hu, Frank B.
    Sun, Qi
    CIRCULATION, 2016, 133 (24) : 2370 - +
  • [25] Lowered cognitive function and the risk of the first events of cardiovascular diseases: findings from a cohort study in Lithuania
    Luksiene, Dalia
    Sapranaviciute-Zabazlajeva, Laura
    Tamosiunas, Abdonas
    Radisauskas, Ricardas
    Bobak, Martin
    BMC PUBLIC HEALTH, 2021, 21 (01) : 792
  • [26] Evidence from prospective cohort studies did not support the introduction of dietary fat guidelines in 1977 and 1983: a systematic review
    Harcombe, Zoe
    Baker, Julien S.
    Davies, Bruce
    BRITISH JOURNAL OF SPORTS MEDICINE, 2017, 51 (24) : 1736 - +
  • [27] Heart Rate Recovery and Risk of Cardiovascular Events and All-Cause Mortality: A Meta-Analysis of Prospective Cohort Studies
    Qiu, Shanhu
    Cai, Xue
    Sun, Zilin
    Li, Ling
    Zuegel, Martina
    Steinacker, Juergen Michael
    Schumann, Uwe
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2017, 6 (05):
  • [28] Dynamic Changes of Metabolic Syndrome Alter the Risks of Cardiovascular Diseases and All-Cause Mortality: Evidence From a Prospective Cohort Study
    He, Di
    Zhang, Xuhui
    Chen, Shuohua
    Dai, Chen
    Wu, Qiong
    Zhou, Yaohan
    Jin, Ziqi
    Wu, Shouling
    Zhu, Yimin
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2021, 8
  • [29] Fruit consumption and risk of type 2 diabetes: results from three prospective longitudinal cohort studies
    Muraki, Isao
    Imamura, Fumiaki
    Manson, JoAnn E.
    Hu, Frank B.
    Willett, Walter C.
    van Dam, Rob M.
    Sun, Qi
    BMJ-BRITISH MEDICAL JOURNAL, 2013, 347
  • [30] Morning plasma cortisol as a cardiovascular risk factor: findings from prospective cohort and Mendelian randomization studies
    Crawford, Andrew A.
    Soderberg, Stefan
    Kirschbaum, Clemens
    Murphy, Lee
    Eliasson, Mats
    Ebrahim, Shah
    Smith, George Davey
    Olsson, Tommy
    Sattar, Naveed
    Lawlor, Debbie A.
    Timpson, Nicolas J.
    Reynolds, Rebecca M.
    Walker, Brian R.
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2019, 181 (04) : 429 - 438