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Serum N (1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients
BACKGROUND: We previously reported that serum N (1)‐methylnicotinamide (me‐Nam), an indicator of nicotinamide N‐methyltransferase activity, is associated with obesity and diabetes mellitus in Chinese patients. However, whether nicotinamide N‐methyltransferase plays a role in human coronary artery di...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523749/ https://www.ncbi.nlm.nih.gov/pubmed/28174167 http://dx.doi.org/10.1161/JAHA.116.004328 |
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author | Liu, Ming Chu, Jihong Gu, Yang Shi, Haibo Zhang, Rusheng Wang, Lingzhun Chen, Jiandong Shen, Le Yu, Peng Chen, Xiaohu Ju, Wenzheng Wang, Zhenxing |
author_facet | Liu, Ming Chu, Jihong Gu, Yang Shi, Haibo Zhang, Rusheng Wang, Lingzhun Chen, Jiandong Shen, Le Yu, Peng Chen, Xiaohu Ju, Wenzheng Wang, Zhenxing |
author_sort | Liu, Ming |
collection | PubMed |
description | BACKGROUND: We previously reported that serum N (1)‐methylnicotinamide (me‐Nam), an indicator of nicotinamide N‐methyltransferase activity, is associated with obesity and diabetes mellitus in Chinese patients. However, whether nicotinamide N‐methyltransferase plays a role in human coronary artery disease (CAD) remains to be elucidated. We aim to investigate the associations of serum me‐Nam with CAD in Chinese patients. METHODS AND RESULTS: Serum me‐NAM was measured by liquid chromatography‐mass spectrometry in patients with (n=230) or without (n=103) CAD as defined by coronary angiography. The severity of CAD was expressed by number of diseased coronary arteries. Serum me‐Nam was higher (7.65 ng/mL versus 4.95 ng/mL, P<0.001) in patients with CAD than in those without. Serum me‐Nam was positively correlated with high‐sensitivity C‐reactive protein and negatively correlated with high‐density lipoprotein before and after adjustment for potential confounding variables (P≤0.002). In multivariable logistic regression analyses, compared with those in the lowest tertile of serum me‐NAM levels, patients in the top tertile had the highest risks for CAD (odds ratio, 4.21; 95% CI, 1.97–8.97 [P<0.001]). After adjustment for potential confounding variables, serum me‐NAM was also increased from 0‐ to 3‐vessel disease (P for trend=0.01). CONCLUSIONS: Serum me‐Nam is strongly associated with presence and severity of CAD, suggesting nicotinamide N‐methyltransferase as a potential target for treating atherosclerosis in humans. |
format | Online Article Text |
id | pubmed-5523749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55237492017-08-14 Serum N (1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients Liu, Ming Chu, Jihong Gu, Yang Shi, Haibo Zhang, Rusheng Wang, Lingzhun Chen, Jiandong Shen, Le Yu, Peng Chen, Xiaohu Ju, Wenzheng Wang, Zhenxing J Am Heart Assoc Original Research BACKGROUND: We previously reported that serum N (1)‐methylnicotinamide (me‐Nam), an indicator of nicotinamide N‐methyltransferase activity, is associated with obesity and diabetes mellitus in Chinese patients. However, whether nicotinamide N‐methyltransferase plays a role in human coronary artery disease (CAD) remains to be elucidated. We aim to investigate the associations of serum me‐Nam with CAD in Chinese patients. METHODS AND RESULTS: Serum me‐NAM was measured by liquid chromatography‐mass spectrometry in patients with (n=230) or without (n=103) CAD as defined by coronary angiography. The severity of CAD was expressed by number of diseased coronary arteries. Serum me‐Nam was higher (7.65 ng/mL versus 4.95 ng/mL, P<0.001) in patients with CAD than in those without. Serum me‐Nam was positively correlated with high‐sensitivity C‐reactive protein and negatively correlated with high‐density lipoprotein before and after adjustment for potential confounding variables (P≤0.002). In multivariable logistic regression analyses, compared with those in the lowest tertile of serum me‐NAM levels, patients in the top tertile had the highest risks for CAD (odds ratio, 4.21; 95% CI, 1.97–8.97 [P<0.001]). After adjustment for potential confounding variables, serum me‐NAM was also increased from 0‐ to 3‐vessel disease (P for trend=0.01). CONCLUSIONS: Serum me‐Nam is strongly associated with presence and severity of CAD, suggesting nicotinamide N‐methyltransferase as a potential target for treating atherosclerosis in humans. John Wiley and Sons Inc. 2017-02-08 /pmc/articles/PMC5523749/ /pubmed/28174167 http://dx.doi.org/10.1161/JAHA.116.004328 Text en © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Liu, Ming Chu, Jihong Gu, Yang Shi, Haibo Zhang, Rusheng Wang, Lingzhun Chen, Jiandong Shen, Le Yu, Peng Chen, Xiaohu Ju, Wenzheng Wang, Zhenxing Serum N (1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients |
title | Serum N
(1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients |
title_full | Serum N
(1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients |
title_fullStr | Serum N
(1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients |
title_full_unstemmed | Serum N
(1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients |
title_short | Serum N
(1)‐Methylnicotinamide is Associated With Coronary Artery Disease in Chinese Patients |
title_sort | serum n
(1)‐methylnicotinamide is associated with coronary artery disease in chinese patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523749/ https://www.ncbi.nlm.nih.gov/pubmed/28174167 http://dx.doi.org/10.1161/JAHA.116.004328 |
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