Impaired lung function is associated with non-alcoholic fatty liver disease independently of metabolic syndrome features in middle-aged and elderly Chinese

Background Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged...

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Published inBMC endocrine disorders Vol. 17; no. 1; p. 18
Main Authors Qin, Li, Zhang, Weiwei, Yang, Zhen, Niu, Yixin, Li, Xiaoyong, Lu, Shuai, Xing, Yin, Lin, Ning, Zhang, Hongmei, Ning, Guang, Fan, Jiangao, Su, Qing
Format Journal Article
LanguageEnglish
Published London BioMed Central 22.03.2017
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ISSN1472-6823
1472-6823
DOI10.1186/s12902-017-0168-4

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Abstract Background Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged and elderly Chinese. Methods A total of 1842 participants aged 40 years or older were recruited from Chongming District, Shanghai, China. Lung function, evaluated by forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) was measured with standard spirometry. The NAFLD was evaluated by ultrasonography. Results The subjects with NAFLD had lower FVC (% predicted) (0.85 ± 0.26 vs. 0.90 ± 0.28, p  < 0.001) and FEV1 (% predicted) (0.93 ± 0.29 vs. 0.98 ± 0.34, p  < 0.001) than non-NAFLD. After adjusting for potential risk factors, the lowest quartile of FVC (% predicted) and FEV1 (% predicted) was associated with increased prevalence of NAFLD, with the fully adjusted odds ratio of 1.37 and 1.24 (95% confidence interval [CI] 1.18–1.97, p  < 0.001, 95% CI 1.11–1.87, p  = 0.009), respectively. Conclusions Impaired lung function is associated with non-alcoholic fatty liver disease, independent of conventional metabolic risk factors.
AbstractList Background Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged and elderly Chinese. Methods A total of 1842 participants aged 40 years or older were recruited from Chongming District, Shanghai, China. Lung function, evaluated by forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) was measured with standard spirometry. The NAFLD was evaluated by ultrasonography. Results The subjects with NAFLD had lower FVC (% predicted) (0.85 ± 0.26 vs. 0.90 ± 0.28, p < 0.001) and FEV1 (% predicted) (0.93 ± 0.29 vs. 0.98 ± 0.34, p < 0.001) than non-NAFLD. After adjusting for potential risk factors, the lowest quartile of FVC (% predicted) and FEV1 (% predicted) was associated with increased prevalence of NAFLD, with the fully adjusted odds ratio of 1.37 and 1.24 (95% confidence interval [CI] 1.18-1.97, p < 0.001, 95% CI 1.11-1.87, p = 0.009), respectively. Conclusions Impaired lung function is associated with non-alcoholic fatty liver disease, independent of conventional metabolic risk factors.
Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged and elderly Chinese.BACKGROUNDAssociations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged and elderly Chinese.A total of 1842 participants aged 40 years or older were recruited from Chongming District, Shanghai, China. Lung function, evaluated by forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) was measured with standard spirometry. The NAFLD was evaluated by ultrasonography.METHODSA total of 1842 participants aged 40 years or older were recruited from Chongming District, Shanghai, China. Lung function, evaluated by forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) was measured with standard spirometry. The NAFLD was evaluated by ultrasonography.The subjects with NAFLD had lower FVC (% predicted) (0.85 ± 0.26 vs. 0.90 ± 0.28, p < 0.001) and FEV1 (% predicted) (0.93 ± 0.29 vs. 0.98 ± 0.34, p < 0.001) than non-NAFLD. After adjusting for potential risk factors, the lowest quartile of FVC (% predicted) and FEV1 (% predicted) was associated with increased prevalence of NAFLD, with the fully adjusted odds ratio of 1.37 and 1.24 (95% confidence interval [CI] 1.18-1.97, p < 0.001, 95% CI 1.11-1.87, p = 0.009), respectively.RESULTSThe subjects with NAFLD had lower FVC (% predicted) (0.85 ± 0.26 vs. 0.90 ± 0.28, p < 0.001) and FEV1 (% predicted) (0.93 ± 0.29 vs. 0.98 ± 0.34, p < 0.001) than non-NAFLD. After adjusting for potential risk factors, the lowest quartile of FVC (% predicted) and FEV1 (% predicted) was associated with increased prevalence of NAFLD, with the fully adjusted odds ratio of 1.37 and 1.24 (95% confidence interval [CI] 1.18-1.97, p < 0.001, 95% CI 1.11-1.87, p = 0.009), respectively.Impaired lung function is associated with non-alcoholic fatty liver disease, independent of conventional metabolic risk factors.CONCLUSIONSImpaired lung function is associated with non-alcoholic fatty liver disease, independent of conventional metabolic risk factors.
Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged and elderly Chinese. A total of 1842 participants aged 40 years or older were recruited from Chongming District, Shanghai, China. Lung function, evaluated by forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) was measured with standard spirometry. The NAFLD was evaluated by ultrasonography. The subjects with NAFLD had lower FVC (% predicted) (0.85 ± 0.26 vs. 0.90 ± 0.28, p < 0.001) and FEV1 (% predicted) (0.93 ± 0.29 vs. 0.98 ± 0.34, p < 0.001) than non-NAFLD. After adjusting for potential risk factors, the lowest quartile of FVC (% predicted) and FEV1 (% predicted) was associated with increased prevalence of NAFLD, with the fully adjusted odds ratio of 1.37 and 1.24 (95% confidence interval [CI] 1.18-1.97, p < 0.001, 95% CI 1.11-1.87, p = 0.009), respectively. Impaired lung function is associated with non-alcoholic fatty liver disease, independent of conventional metabolic risk factors.
Background Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the relationship is scarce. The objective of the study was to evaluate the relationship between lung function and NAFLD in middle-aged and elderly Chinese. Methods A total of 1842 participants aged 40 years or older were recruited from Chongming District, Shanghai, China. Lung function, evaluated by forced vital capacity (FVC) and forced expiratory volume in one second (FEV1) was measured with standard spirometry. The NAFLD was evaluated by ultrasonography. Results The subjects with NAFLD had lower FVC (% predicted) (0.85 ± 0.26 vs. 0.90 ± 0.28, p  < 0.001) and FEV1 (% predicted) (0.93 ± 0.29 vs. 0.98 ± 0.34, p  < 0.001) than non-NAFLD. After adjusting for potential risk factors, the lowest quartile of FVC (% predicted) and FEV1 (% predicted) was associated with increased prevalence of NAFLD, with the fully adjusted odds ratio of 1.37 and 1.24 (95% confidence interval [CI] 1.18–1.97, p  < 0.001, 95% CI 1.11–1.87, p  = 0.009), respectively. Conclusions Impaired lung function is associated with non-alcoholic fatty liver disease, independent of conventional metabolic risk factors.
ArticleNumber 18
Author Yang, Zhen
Lu, Shuai
Fan, Jiangao
Li, Xiaoyong
Zhang, Hongmei
Zhang, Weiwei
Xing, Yin
Lin, Ning
Su, Qing
Qin, Li
Niu, Yixin
Ning, Guang
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Keywords Chinese
Metabolic risk factors
Lung function
Non-alcoholic fatty liver disease
Language English
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Snippet Background Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations...
Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations about the...
Background Associations between lung function and non-alcoholic fatty liver disease (NAFLD) have been reported. However, evidence from large-scale populations...
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StartPage 18
SubjectTerms Aged
Body mass index
Cardiovascular disease
China - epidemiology
Cholesterol
Cross-Sectional Studies
Diabetes
Endocrinology
Epidemiology of Endocrine Disorders
Family medical history
Fasting
Fatty liver
Female
Geriatrics
Glucose
Health risk assessment
Homeostasis
Humans
Inflammation
Insulin resistance
Lipoproteins
Liver diseases
Longitudinal Studies
Lung - diagnostic imaging
Lung - physiopathology
Lungs
Male
Medicine
Medicine & Public Health
Metabolic Diseases
Metabolic syndrome
Metabolic Syndrome - diagnostic imaging
Metabolic Syndrome - epidemiology
Metabolic Syndrome - physiopathology
Middle age
Middle Aged
Non-alcoholic Fatty Liver Disease - diagnostic imaging
Non-alcoholic Fatty Liver Disease - epidemiology
Non-alcoholic Fatty Liver Disease - physiopathology
Plasma
Research Article
Respiratory function
Respiratory Function Tests - methods
Risk factors
rology
Single-Blind Method
Studies
Ultrasound
Vital Capacity - physiology
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Title Impaired lung function is associated with non-alcoholic fatty liver disease independently of metabolic syndrome features in middle-aged and elderly Chinese
URI https://link.springer.com/article/10.1186/s12902-017-0168-4
https://www.ncbi.nlm.nih.gov/pubmed/28330472
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https://pubmed.ncbi.nlm.nih.gov/PMC5361719
https://bmcendocrdisord.biomedcentral.com/track/pdf/10.1186/s12902-017-0168-4
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