PMID- 29863106 OWN - NLM STAT- MEDLINE DCOM- 20181016 LR - 20181202 IS - 1643-3750 (Electronic) IS - 1234-1010 (Print) IS - 1234-1010 (Linking) VI - 24 DP - 2018 Jun 4 TI - Synergistic Effect of Atorvastatin and Folic Acid on Cardiac Function and Ventricular Remodeling in Chronic Heart Failure Patients with Hyperhomocysteinemia. PG - 3744-3751 LID - 10.12659/MSM.906893 [doi] AB - BACKGROUND At present, a constant progress in pathophysiology understanding and treatment of the chronic heart failure (CHF) is arising. Meanwhile, hyperhomocysteinemia (HHcy) has been linked to impaired left ventricular function and clinical class in patients with CHF. Atorvastatin therapy can reduce the incidence of sudden cardiac death in patients with advanced CHF. Folic acid could enhance endothelial function in vascular disease states. The present study aims to investigate the effect of atorvastatin and folic acid combined on the cardiac function and ventricular remodeling in CHF patients with HHcy. MATERIAL AND METHODS Elderly CHF patients with HHcy were divided into four groups: routine, routine + atorvastatin, routine + folic acid, and routine + atorvastatin + folic acid groups. Serum homocysteine (Hcy) level was detected using enzymatic cycling methods, and N-terminal pro brain natriuretic peptide (NT-proBNP) level by ELISA. The cardiac function indexes and left ventricular early diastolic peak flow velocity/atrial systolic peak flow velocity (E/A) ratio were evaluated. The six-minute walk test was performed to measure the six-minute walk distance (6MWD). RESULTS 6MWD increased, the serum Hcy and NT-proBNP levels decreased, and cardiac function was improved compared with before treatment, which was the most significant in the routine + atorvastatin + folic acid group, followed by the routine + atorvastatin group, then the routine + folic acid group, and lastly, the routine group. CONCLUSIONS The results indicated that the combination of atorvastatin and folic acid improved the cardiac function and inhibited ventricular remodeling of elderly CHF patients with HHcy. FAU - Peng, You AU - Peng Y AD - Department of Geriatric, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). FAU - Ou, Bai-Qing AU - Ou BQ AD - Department of Geriatric, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). FAU - Li, Hua-Hua AU - Li HH AD - Department of Geriatric, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). FAU - Zhou, Zhi AU - Zhou Z AD - Department of Cardiology, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). FAU - Mo, Jiong-Ling AU - Mo JL AD - Department of Geriatric, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). FAU - Huang, Jue AU - Huang J AD - Department of Cardiology, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). FAU - Liang, Feng-Ling AU - Liang FL AD - Department of Cardiology, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, China (mainland). LA - eng PT - Journal Article DEP - 20180604 PL - United States TA - Med Sci Monit JT - Medical science monitor : international medical journal of experimental and clinical research JID - 9609063 RN - 935E97BOY8 (Folic Acid) RN - A0JWA85V8F (Atorvastatin) SB - IM MH - Aged MH - Aged, 80 and over MH - Atorvastatin/metabolism/pharmacology/*therapeutic use MH - China MH - Chronic Disease MH - Female MH - Folic Acid/metabolism/pharmacology/*therapeutic use MH - Heart Failure/drug therapy/physiopathology MH - Heart Function Tests/drug effects MH - Humans MH - Hyperhomocysteinemia/*drug therapy MH - Male MH - Middle Aged MH - Ventricular Remodeling/drug effects PMC - PMC6015480 COIS- Conflicts of interests None. EDAT- 2018/06/05 06:00 MHDA- 2018/10/17 06:00 PMCR- 2018/06/04 CRDT- 2018/06/05 06:00 PHST- 2018/06/05 06:00 [entrez] PHST- 2018/06/05 06:00 [pubmed] PHST- 2018/10/17 06:00 [medline] PHST- 2018/06/04 00:00 [pmc-release] AID - 906893 [pii] AID - 10.12659/MSM.906893 [doi] PST - epublish SO - Med Sci Monit. 2018 Jun 4;24:3744-3751. doi: 10.12659/MSM.906893.