Additive clinical value of serum brain-derived neurotrophic factor for prediction of chronic heart failure outcome
The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotect...
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Published in | Heart and vessels Vol. 31; no. 4; pp. 535 - 544 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Tokyo
Springer Japan
01.04.2016
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0910-8327 1615-2573 1615-2573 |
DOI | 10.1007/s00380-015-0628-6 |
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Abstract | The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotective role, we elucidated whether BDNF is associated with cardiovascular events in patients with chronic heart failure (CHF). We examined serum BDNF levels in 134 patients with CHF and 23 control subjects. The patients were followed to register cardiac events for a median of 426 days. BDNF was significantly lower in CHF patients than in control subjects (25.8 ± 8.4 vs 14.7 ± 8.4,
P
< 0.0001). Serum BDNF was also lower in patients with cardiac events than in event-free patients (16.1 ± 8.0 vs 12.5 ± 8.5,
P
< 0.0001). The cutoff value of BDNF was determined by performing receiver operating characteristic curve analysis. Kaplan–Meier analysis demonstrated that patients with low levels of BDNF experienced higher rates of cardiac events than those with high levels of BDNF. Multivariate Cox hazard analysis demonstrated that low BDNF levels (≤12.4 ng/mL) were an independent prognostic factor for cardiac events (hazard ratio 2.932, 95 % confidence interval 1.622–5.301;
P
= 0.0004). Adding levels of BDNF to the model with BNP levels, age, and eGFR for the prediction of cardiac events yielded significant net reclassification improvement of 0.429 (
P
< 0.001) and an integrated discrimination improvement of 0.101 (
P
< 0.001). Low serum BDNF levels were found in patients with CHF, and these levels were found to be independently associated with an increased risk of cardiac events. |
---|---|
AbstractList | The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotective role, we elucidated whether BDNF is associated with cardiovascular events in patients with chronic heart failure (CHF). We examined serum BDNF levels in 134 patients with CHF and 23 control subjects. The patients were followed to register cardiac events for a median of 426 days. BDNF was significantly lower in CHF patients than in control subjects (25.8 ± 8.4 vs 14.7 ± 8.4, P < 0.0001). Serum BDNF was also lower in patients with cardiac events than in event-free patients (16.1 ± 8.0 vs 12.5 ± 8.5, P < 0.0001). The cutoff value of BDNF was determined by performing receiver operating characteristic curve analysis. Kaplan-Meier analysis demonstrated that patients with low levels of BDNF experienced higher rates of cardiac events than those with high levels of BDNF. Multivariate Cox hazard analysis demonstrated that low BDNF levels ([less than or equal to]12.4 ng/mL) were an independent prognostic factor for cardiac events (hazard ratio 2.932, 95 % confidence interval 1.622-5.301; P = 0.0004). Adding levels of BDNF to the model with BNP levels, age, and eGFR for the prediction of cardiac events yielded significant net reclassification improvement of 0.429 (P < 0.001) and an integrated discrimination improvement of 0.101 (P < 0.001). Low serum BDNF levels were found in patients with CHF, and these levels were found to be independently associated with an increased risk of cardiac events. The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotective role, we elucidated whether BDNF is associated with cardiovascular events in patients with chronic heart failure (CHF). We examined serum BDNF levels in 134 patients with CHF and 23 control subjects. The patients were followed to register cardiac events for a median of 426 days. BDNF was significantly lower in CHF patients than in control subjects (25.8 ± 8.4 vs 14.7 ± 8.4, P < 0.0001). Serum BDNF was also lower in patients with cardiac events than in event-free patients (16.1 ± 8.0 vs 12.5 ± 8.5, P < 0.0001). The cutoff value of BDNF was determined by performing receiver operating characteristic curve analysis. Kaplan–Meier analysis demonstrated that patients with low levels of BDNF experienced higher rates of cardiac events than those with high levels of BDNF. Multivariate Cox hazard analysis demonstrated that low BDNF levels (≤12.4 ng/mL) were an independent prognostic factor for cardiac events (hazard ratio 2.932, 95 % confidence interval 1.622–5.301; P = 0.0004). Adding levels of BDNF to the model with BNP levels, age, and eGFR for the prediction of cardiac events yielded significant net reclassification improvement of 0.429 ( P < 0.001) and an integrated discrimination improvement of 0.101 ( P < 0.001). Low serum BDNF levels were found in patients with CHF, and these levels were found to be independently associated with an increased risk of cardiac events. The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotective role, we elucidated whether BDNF is associated with cardiovascular events in patients with chronic heart failure (CHF). We examined serum BDNF levels in 134 patients with CHF and 23 control subjects. The patients were followed to register cardiac events for a median of 426 days. BDNF was significantly lower in CHF patients than in control subjects (25.8 ± 8.4 vs 14.7 ± 8.4, P < 0.0001). Serum BDNF was also lower in patients with cardiac events than in event-free patients (16.1 ± 8.0 vs 12.5 ± 8.5, P < 0.0001). The cutoff value of BDNF was determined by performing receiver operating characteristic curve analysis. Kaplan-Meier analysis demonstrated that patients with low levels of BDNF experienced higher rates of cardiac events than those with high levels of BDNF. Multivariate Cox hazard analysis demonstrated that low BDNF levels (≤12.4 ng/mL) were an independent prognostic factor for cardiac events (hazard ratio 2.932, 95 % confidence interval 1.622-5.301; P = 0.0004). Adding levels of BDNF to the model with BNP levels, age, and eGFR for the prediction of cardiac events yielded significant net reclassification improvement of 0.429 (P < 0.001) and an integrated discrimination improvement of 0.101 (P < 0.001). Low serum BDNF levels were found in patients with CHF, and these levels were found to be independently associated with an increased risk of cardiac events.The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotective role, we elucidated whether BDNF is associated with cardiovascular events in patients with chronic heart failure (CHF). We examined serum BDNF levels in 134 patients with CHF and 23 control subjects. The patients were followed to register cardiac events for a median of 426 days. BDNF was significantly lower in CHF patients than in control subjects (25.8 ± 8.4 vs 14.7 ± 8.4, P < 0.0001). Serum BDNF was also lower in patients with cardiac events than in event-free patients (16.1 ± 8.0 vs 12.5 ± 8.5, P < 0.0001). The cutoff value of BDNF was determined by performing receiver operating characteristic curve analysis. Kaplan-Meier analysis demonstrated that patients with low levels of BDNF experienced higher rates of cardiac events than those with high levels of BDNF. Multivariate Cox hazard analysis demonstrated that low BDNF levels (≤12.4 ng/mL) were an independent prognostic factor for cardiac events (hazard ratio 2.932, 95 % confidence interval 1.622-5.301; P = 0.0004). Adding levels of BDNF to the model with BNP levels, age, and eGFR for the prediction of cardiac events yielded significant net reclassification improvement of 0.429 (P < 0.001) and an integrated discrimination improvement of 0.101 (P < 0.001). Low serum BDNF levels were found in patients with CHF, and these levels were found to be independently associated with an increased risk of cardiac events. The importance of the central nervous system in cardiovascular events has been recognized. Recently, brain-derived neurotrophic factor (BDNF), a member of the neurotrophic factor family, is involved in depression mechanisms and also in stress and anxiety. Because BDNF is reported about cardioprotective role, we elucidated whether BDNF is associated with cardiovascular events in patients with chronic heart failure (CHF). We examined serum BDNF levels in 134 patients with CHF and 23 control subjects. The patients were followed to register cardiac events for a median of 426 days. BDNF was significantly lower in CHF patients than in control subjects (25.8 ± 8.4 vs 14.7 ± 8.4, P < 0.0001). Serum BDNF was also lower in patients with cardiac events than in event-free patients (16.1 ± 8.0 vs 12.5 ± 8.5, P < 0.0001). The cutoff value of BDNF was determined by performing receiver operating characteristic curve analysis. Kaplan-Meier analysis demonstrated that patients with low levels of BDNF experienced higher rates of cardiac events than those with high levels of BDNF. Multivariate Cox hazard analysis demonstrated that low BDNF levels (≤12.4 ng/mL) were an independent prognostic factor for cardiac events (hazard ratio 2.932, 95 % confidence interval 1.622-5.301; P = 0.0004). Adding levels of BDNF to the model with BNP levels, age, and eGFR for the prediction of cardiac events yielded significant net reclassification improvement of 0.429 (P < 0.001) and an integrated discrimination improvement of 0.101 (P < 0.001). Low serum BDNF levels were found in patients with CHF, and these levels were found to be independently associated with an increased risk of cardiac events. |
Author | Narumi, Taro Shishido, Tetsuro Watanabe, Tetsu Honda, Yuki Kadowaki, Shinpei Miyamoto, Takuya Kinoshita, Daisuke Kubota, Isao Takahashi, Hiroki Arimoto, Takanori Otaki, Yoichiro Nishiyama, Satoshi |
Author_xml | – sequence: 1 givenname: Shinpei surname: Kadowaki fullname: Kadowaki, Shinpei organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 2 givenname: Tetsuro surname: Shishido fullname: Shishido, Tetsuro email: tshishid@med.id.yamagata-u.ac.jp organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 3 givenname: Yuki surname: Honda fullname: Honda, Yuki organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 4 givenname: Taro surname: Narumi fullname: Narumi, Taro organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 5 givenname: Yoichiro surname: Otaki fullname: Otaki, Yoichiro organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 6 givenname: Daisuke surname: Kinoshita fullname: Kinoshita, Daisuke organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 7 givenname: Satoshi surname: Nishiyama fullname: Nishiyama, Satoshi organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 8 givenname: Hiroki surname: Takahashi fullname: Takahashi, Hiroki organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 9 givenname: Takanori surname: Arimoto fullname: Arimoto, Takanori organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 10 givenname: Takuya surname: Miyamoto fullname: Miyamoto, Takuya organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 11 givenname: Tetsu surname: Watanabe fullname: Watanabe, Tetsu organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine – sequence: 12 givenname: Isao surname: Kubota fullname: Kubota, Isao organization: Department of Cardiology, Pulmonology, and Nephrology, Yamagata University School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25616498$$D View this record in MEDLINE/PubMed |
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Keywords | Heart failure Brain-derived neurotrophic factor Prognosis Risk stratification |
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SubjectTerms | Aged Biomarkers - blood Biomedical Engineering and Bioengineering Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - blood Cardiac Surgery Cardiology Disease Progression Echocardiography Enzyme-Linked Immunosorbent Assay Female Heart failure Heart Failure - blood Heart Failure - diagnosis Heart Failure - epidemiology Heart Ventricles - diagnostic imaging Humans Incidence Japan - epidemiology Kaplan-Meier Estimate Male Medical prognosis Medicine Medicine & Public Health Original Article Prognosis Radiography, Thoracic Retrospective Studies Risk Factors ROC Curve Survival Rate - trends Vascular Surgery |
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Title | Additive clinical value of serum brain-derived neurotrophic factor for prediction of chronic heart failure outcome |
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