PMID- 24918531 OWN - NLM STAT- MEDLINE DCOM- 20150527 LR - 20140918 IS - 1439-3646 (Electronic) IS - 0947-7349 (Linking) VI - 122 IP - 8 DP - 2014 Sep TI - Fasting blood glucose at admission and survival in patients with dilated cardiomyopathy: a single-center cohort study. PG - 457-62 LID - 10.1055/s-0034-1376966 [doi] AB - BACKGROUND: Recent data have suggested that impaired fasting glucose (IFG) is an independent risk factor for mortality in patients with heart failure. However, the prognostic indicator of elevated fasting blood glucose (FBG) such as IFG in dilated cardiomyopathy (DCM) was not well understood. The purpose of this study was to examine the association between IFG at admission and survival in hospitalized patients with DCM. METHODS: A retrospective cohort study was undertaken in 1 089 hospitalized patients with DCM in Fuwai Hospital from November 2003 to September 2 011 (female 26.5%, 51.4+/-14.6 years old). Standard demographics, echocardiography and routine blood samples were obtained shortly after admission. The outcomes were assessed using all-cause mortality at a mean follow-up of 3.5+/-2.3 years and were analyzed using Kaplan-Meier survival curve (log-rank test) and Cox regression. RESULTS: The cohort consisted of 1 089 patients with DCM, 835 patients with normal fasting glucose (NFG, FBG<6.1 mmol/L, 76.7%), 113 patients with IFG (FBG 6.1-6.9 mmol/L, 10.4%), and 141 patients with FBG>/=7.0 mmol/L (12.9%). Among the 1 089 patients studied, 252 (23.1%) died over a mean follow-up period of 3.5+/-2.3 years. All-cause mortality rates were highest in patients with FBG>/=7.0 mmol/L (31.2%), intermediate in those with IFG (24.8%), and lowest in those with NFG (21.6%); a significant difference in all-cause mortality rate was found among the 3 groups (log-rank chi(2)=6.715, P=0.035). After adjustment for baseline variables, New York Heart Association (NYHA) functional class, QRS duration, left atrium diameter, systolic blood pressure, FBG>/=7.0 mmol/L, not IFG, and circulating creatinine levels were the variables that remained as predictors of all-cause mortality. CONCLUSION: In the present study, all-cause mortality was higher in patients with FBG>/=7.0 mmol/L compared to the patients with NFG, and FBG>/= 7.0 mmol/L, not IFG, was one of predictors of all-cause mortality in DCM patients. CI - (c) J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart . New York. FAU - Li, X AU - Li X AD - Department of Cardiology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China. FAU - Jiang, R AU - Jiang R AD - Department of Cardiology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China. FAU - Kong, H AU - Kong H AD - Department of Cardiology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China. FAU - Shu, Y AU - Shu Y AD - Department of Cardiology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China. FAU - Li, Q AU - Li Q AD - Department of Cardiology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China. FAU - Hua, W AU - Hua W AD - Cardiac Arrhythmia Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for -Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. LA - eng PT - Journal Article PT - Observational Study PT - Research Support, Non-U.S. Gov't DEP - 20140611 PL - Germany TA - Exp Clin Endocrinol Diabetes JT - Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association JID - 9505926 RN - 0 (Blood Glucose) SB - IM MH - Adult MH - Aged MH - Blood Glucose/*analysis MH - Cardiomyopathy, Dilated/*blood/*mortality MH - Cohort Studies MH - Fasting/*blood MH - Female MH - Hospitalization MH - Humans MH - Male MH - Middle Aged MH - Prognosis MH - Retrospective Studies MH - Risk Factors MH - Survival Rate EDAT- 2014/06/12 06:00 MHDA- 2015/05/28 06:00 CRDT- 2014/06/12 06:00 PHST- 2014/06/12 06:00 [entrez] PHST- 2014/06/12 06:00 [pubmed] PHST- 2015/05/28 06:00 [medline] AID - 10.1055/s-0034-1376966 [doi] PST - ppublish SO - Exp Clin Endocrinol Diabetes. 2014 Sep;122(8):457-62. doi: 10.1055/s-0034-1376966. Epub 2014 Jun 11.