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- Publisher Website: 10.1042/CS20120004
- Scopus: eid_2-s2.0-84870748223
- PMID: 23013043
- WOS: WOS:000313406100011
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Article: Circulating adipocyte fatty acid-binding protein levels are independently associated with heart failure
Title | Circulating adipocyte fatty acid-binding protein levels are independently associated with heart failure |
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Authors | |
Keywords | Adipocyte fatty acid-binding protein Echocardiography Heart failure N-terminal pro-brain natriuretic peptide |
Issue Date | 2013 |
Publisher | Portland Press Ltd. The Journal's web site is located at http://www.clinsci.org/ |
Citation | Clinical Science, 2013, v. 124 n. 2, p. 115-122 How to Cite? |
Abstract | A-FABP (adipocyte fatty acid-binding protein), one of the most abundant proteins in adipocytes, plays a key role in obesity-related insulin resistance, inflammation and atherosclerosis in animals. In the present study, we sought to investigate the association of A-FABP with HF (heart failure) in Chinese subjects. Serum A-FABP levels were measured in 252 HF patients and 261 age-, gender- and BMI (body mass index)-matched non-HF subjects. Echocardiography was performed on each patient. The severity of HF was determined by the NYHA (New York Heart Association) classification system. After adjustments for age, gender and BMI, serum A-FABP concentrations in patients with HF were significantly higher than in non-HF patients [11.17 (6.63-19.93) ng/ml compared with 5.67 (3.20-8.87) ng/ml; P<0.001] and significantly progressed with the NYHA class (P<0.001). In addition, NT-proBNP (N-terminal pro-brain natriuretic peptide) was independently and positively correlated with A-FABP (standardized beta=0.340, P<0.001) after adjusting for confounding factors. Each echocardiographic parameter, especially LVEF (left ventricular ejection fraction), was independently associated with A-FABP (all P<0.05). Multivariate logistic regression analysis demonstrated that A-FABP concentration was an independent risk factor for HF [odds ratio, 6.93 (95% confidence interval, 2.49-19.30); P<0.001]. Our results demonstrate that A-FABP is closely associated with HF, and raise the possibility that increased A-FABP may be causally related to the pathogenesis of heart dysfunction in humans. |
Persistent Identifier | http://hdl.handle.net/10722/197233 |
ISSN | 2023 Impact Factor: 6.7 2023 SCImago Journal Rankings: 1.565 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Liu, M | en_US |
dc.contributor.author | Zhou, M | en_US |
dc.contributor.author | Bao, Y | en_US |
dc.contributor.author | Xu, Z | en_US |
dc.contributor.author | Li, H | en_US |
dc.contributor.author | Zhang, H | en_US |
dc.contributor.author | Zhu, W | en_US |
dc.contributor.author | Zhang, J | en_US |
dc.contributor.author | Xu, A | en_US |
dc.contributor.author | Jia, W | en_US |
dc.date.accessioned | 2014-05-23T02:27:37Z | - |
dc.date.available | 2014-05-23T02:27:37Z | - |
dc.date.issued | 2013 | en_US |
dc.identifier.citation | Clinical Science, 2013, v. 124 n. 2, p. 115-122 | en_US |
dc.identifier.issn | 0143-5221 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/197233 | - |
dc.description.abstract | A-FABP (adipocyte fatty acid-binding protein), one of the most abundant proteins in adipocytes, plays a key role in obesity-related insulin resistance, inflammation and atherosclerosis in animals. In the present study, we sought to investigate the association of A-FABP with HF (heart failure) in Chinese subjects. Serum A-FABP levels were measured in 252 HF patients and 261 age-, gender- and BMI (body mass index)-matched non-HF subjects. Echocardiography was performed on each patient. The severity of HF was determined by the NYHA (New York Heart Association) classification system. After adjustments for age, gender and BMI, serum A-FABP concentrations in patients with HF were significantly higher than in non-HF patients [11.17 (6.63-19.93) ng/ml compared with 5.67 (3.20-8.87) ng/ml; P<0.001] and significantly progressed with the NYHA class (P<0.001). In addition, NT-proBNP (N-terminal pro-brain natriuretic peptide) was independently and positively correlated with A-FABP (standardized beta=0.340, P<0.001) after adjusting for confounding factors. Each echocardiographic parameter, especially LVEF (left ventricular ejection fraction), was independently associated with A-FABP (all P<0.05). Multivariate logistic regression analysis demonstrated that A-FABP concentration was an independent risk factor for HF [odds ratio, 6.93 (95% confidence interval, 2.49-19.30); P<0.001]. Our results demonstrate that A-FABP is closely associated with HF, and raise the possibility that increased A-FABP may be causally related to the pathogenesis of heart dysfunction in humans. | en_US |
dc.language | eng | en_US |
dc.publisher | Portland Press Ltd. The Journal's web site is located at http://www.clinsci.org/ | en_US |
dc.relation.ispartof | Clinical Science | en_US |
dc.rights | The final version of record is available at [Journal URL]. | en_US |
dc.subject | Adipocyte fatty acid-binding protein | - |
dc.subject | Echocardiography | - |
dc.subject | Heart failure | - |
dc.subject | N-terminal pro-brain natriuretic peptide | - |
dc.subject.mesh | Analysis of Variance | en_US |
dc.subject.mesh | Anthropometry | en_US |
dc.subject.mesh | Body Mass Index | en_US |
dc.subject.mesh | Fatty Acid-Binding Proteins - blood | en_US |
dc.subject.mesh | Heart Failure - blood | en_US |
dc.title | Circulating adipocyte fatty acid-binding protein levels are independently associated with heart failure | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zhang, J: hjzhang@hkucc.hku.hk | en_US |
dc.identifier.email | Xu, A: amxu@hkucc.hku.hk | en_US |
dc.identifier.authority | Xu, A=rp00485 | en_US |
dc.identifier.doi | 10.1042/CS20120004 | en_US |
dc.identifier.pmid | 23013043 | en_US |
dc.identifier.scopus | eid_2-s2.0-84870748223 | - |
dc.identifier.hkuros | 221753 | en_US |
dc.identifier.volume | 124 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 115 | en_US |
dc.identifier.epage | 122 | en_US |
dc.identifier.isi | WOS:000313406100011 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.issnl | 0143-5221 | - |