PMID- 17183715 OWN - NLM STAT- MEDLINE DCOM- 20100316 LR - 20181113 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 1 IP - 1 DP - 2006 Dec 20 TI - Hyperhomocysteinemia and mortality after coronary artery bypass grafting. PG - e83 LID - e83 AB - BACKGROUND: The independent prognostic impact, as well as the possible causal role, of hyperhomocysteinemia (HHcy) in coronary artery disease (CAD) is controversial. No previous study specifically has addressed the relationship between HHcy and mortality after coronary artery bypass grafting (CABG) surgery. The aim of this study is to evaluate the prognostic impact of HHcy after CABG surgery. METHODOLOGY AND PRINCIPAL FINDINGS: We prospectively followed 350 patients who underwent elective CABG between May 1996 and May 1999. At baseline, fasting total homocysteine (tHcy) levels were measured in all participants, and a post-methionine loading (PML) test was performed in 77.7% of them (n = 272). After a median follow-up of 58 months, 33 patients (9.4%) had died, 25 because of cardiovascular events. HHcy, defined by levels higher than the 90th percentile (25.2 micromol/L) of the population's distribution, was significantly associated to total and cardiovascular mortality (P = 0.018 [log-rank test 5.57]; P = 0.002 [log-rank test 9.76], respectively). The PML test had no prognostic value. After multiple adjustment for other univariate predictors by Cox regression, including statin therapy (the most powerful predictor in uni-/multivariate analyses), high-sensitivity C Reactive Protein (hs-CRP) levels, and all known major genetic (MTHFR 677C-->T polymorphism) and non-genetic (B-group vitamin status and renal function) tHcy determinants, HHcy remained an independent prognostic factor for mortality (HRs: 5.02, 95% CIs 1.88 to 13.42, P = 0.001). CONCLUSIONS: HHcy is an important prognostic marker after CABG, independent of modern drug therapy and biomarkers. FAU - Girelli, Domenico AU - Girelli D AD - Department of Clinical and Experimental Medicine, University of Verona, Italy. domenico.girelli@univr.it FAU - Martinelli, Nicola AU - Martinelli N FAU - Olivieri, Oliviero AU - Olivieri O FAU - Pizzolo, Francesca AU - Pizzolo F FAU - Friso, Simonetta AU - Friso S FAU - Faccini, Giovanni AU - Faccini G FAU - Bozzini, Claudia AU - Bozzini C FAU - Tenuti, Ilaria AU - Tenuti I FAU - Lotto, Valentina AU - Lotto V FAU - Villa, Giuliano AU - Villa G FAU - Guarini, Patrizia AU - Guarini P FAU - Trabetti, Elisabetta AU - Trabetti E FAU - Pignatti, Pier Franco AU - Pignatti PF FAU - Mazzucco, Alessandro AU - Mazzucco A FAU - Corrocher, Roberto AU - Corrocher R LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20061220 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0LVT1QZ0BA (Homocysteine) RN - EC 1.5.1.20 (Methylenetetrahydrofolate Reductase (NADPH2)) SB - IM MH - Aged MH - Coronary Artery Bypass/*mortality MH - Coronary Artery Disease/*complications/mortality/*surgery MH - Female MH - Genotype MH - Homocysteine/blood MH - Humans MH - Hyperhomocysteinemia/blood/*complications/enzymology/genetics MH - Italy/epidemiology MH - Male MH - Methylenetetrahydrofolate Reductase (NADPH2)/genetics MH - Middle Aged MH - Multivariate Analysis MH - Prognosis MH - Proportional Hazards Models MH - Prospective Studies MH - Risk Factors PMC - PMC1762373 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2006/12/22 09:00 MHDA- 2006/12/22 09:01 PMCR- 2006/12/20 CRDT- 2006/12/22 09:00 PHST- 2006/10/18 00:00 [received] PHST- 2006/11/09 00:00 [accepted] PHST- 2006/12/22 09:00 [pubmed] PHST- 2006/12/22 09:01 [medline] PHST- 2006/12/22 09:00 [entrez] PHST- 2006/12/20 00:00 [pmc-release] AID - 06-PONE-RA-00253 [pii] AID - 10.1371/journal.pone.0000083 [doi] PST - epublish SO - PLoS One. 2006 Dec 20;1(1):e83. doi: 10.1371/journal.pone.0000083.