Literature DB >> 16612246

Hyperhomocysteinemia predicts total and cardiovascular mortality in high-risk women.

Gian Paolo Rossi1, Giuseppe Maiolino, Teresa Maria Seccia, Alberto Burlina, Silvia Zavattiero, Maurizio Cesari, Daniele Sticchi, Luigi Pedon, Mario Zanchetta, Achille C Pessina.   

Abstract

OBJECTIVE: The impact of homocysteine on cardiovascular disease can be more detrimental in women than in men, but it is unknown whether this applies to high-risk women. We therefore investigated the association of hyperhomocysteinemia with coronary artery disease (CAD) and cardiovascular mortality in high-risk women referred for CAD, both in the total population and in the hypertensive and normotensive cohorts.
DESIGN: A prospective study cohort.
SETTING: A tertiary centre. INCLUSION CRITERIA: 262 consecutive Caucasian postmenopausal women referred for coronary angiography. EXCLUSION CRITERIA: acute myocardial infarction and vitamin supplementation. MAIN OUTCOME MEASURE(S): We assessed total plasma homocysteine (tHcy), folate levels, and the MTHFR677C-->T polymorphism. CAD was defined as a modified Duke Index score greater than 0; hyperhomocysteinemia as tHcy levels of 15 micromol/l or greater. The primary study outcome was cardiovascular mortality at follow-up.
RESULTS: Mild/moderate and severe hyperhomocysteinemia was found in 15.1 and 1.6% of women, respectively, without differences between CAD and non-CAD women. By the ATPIII criteria, 92.2% of the women were in the highest risk class and 55% had CAD; however, no association of tHcy with the CAD score was found. After a median follow-up of 3.6 years, 23 women (9.1%) had died, 15 (6%) of cardiovascular causes. Women with high tHcy levels showed the worst all-cause and cardiovascular death-free survival at Kaplan-Meier and Cox regression analysis. Moreover, in the hypertensive cohort only women with hyperhomocysteinemia showed increased cardiovascular mortality.
CONCLUSION: Hyperhomocysteinemia is common in high-risk women and adversely affects their prognosis, although it is unrelated to the CAD atherosclerotic burden.

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Year:  2006        PMID: 16612246     DOI: 10.1097/01.hjh.0000222754.75196.5c

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  7 in total

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Authors:  Hui-yong Peng; Chang-feng Man; Juan Xu; Yu Fan
Journal:  J Zhejiang Univ Sci B       Date:  2015-01       Impact factor: 3.066

2.  Biochemical risk indices, including plasma homocysteine, that prospectively predict mortality in older British people: the National Diet and Nutrition Survey of People Aged 65 Years and Over.

Authors:  Christopher J Bates; Mohammed A Mansoor; Kristina D Pentieva; Mark Hamer; Gita D Mishra
Journal:  Br J Nutr       Date:  2010-04-19       Impact factor: 3.718

3.  Homocysteine is associated with plasma high-sensitivity cardiac troponin T levels in a community-dwelling population.

Authors:  Ruihua Cao; Yongyi Bai; Ruyi Xu; Ping Ye
Journal:  Clin Interv Aging       Date:  2013-12-27       Impact factor: 4.458

4.  Red cell distribution width and homocysteine act as independent risk factors for cardiovascular events in newly diagnostic essential hypertension.

Authors:  Lian-Man He; Chuan-Yu Gao; Yong Wang; Hao Wang; Hai-Ying Zhao
Journal:  Oncotarget       Date:  2017-10-21

5.  Hyperhomocysteinemia Increases Risk of Metabolic Syndrome and Cardiovascular Death in an Elderly Chinese Community Population of a 7-Year Follow-Up Study.

Authors:  Chang Liu; Liping Liu; Yinglu Wang; Xiaoli Chen; Jie Liu; Sheng Peng; Jingjiang Pi; Qi Zhang; Brain Tomlinson; Paul Chan; Lin Zhang; Huimin Fan; Liang Zheng; Zhongmin Liu; Yuzhen Zhang
Journal:  Front Cardiovasc Med       Date:  2022-02-10

6.  Use of serum homocysteine to predict cardiovascular disease in Korean men with or without metabolic syndrome.

Authors:  Ji Yeon Kang; Ill Keun Park; Ji Young Lee; Sook Hee Sung; Youn Koun Chang; Yoo Kyoung Park; Tae In Choi
Journal:  J Korean Med Sci       Date:  2012-04-25       Impact factor: 2.153

7.  Homocysteine and all-cause mortality in hypertensive adults without pre-existing cardiovascular conditions: Effect modification by MTHFR C677T polymorphism.

Authors:  Benjamin Xu; Xiangyi Kong; Richard Xu; Yun Song; Lishun Liu; Ziyi Zhou; Rui Gu; Xiuli Shi; Min Zhao; Xiao Huang; Mingli He; Jia Fu; Yefeng Cai; Ping Li; Xiaoshu Cheng; Changyan Wu; Fang Chen; Yan Zhang; Genfu Tang; Xianhui Qin; Binyan Wang; Hao Xue; Yundai Chen; Ye Tian; Ningling Sun; Yimin Cui; Fan Fan Hou; Jianping Li; Yong Huo
Journal:  Medicine (Baltimore)       Date:  2017-02       Impact factor: 1.817

  7 in total

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