PMID- 31714330 OWN - NLM STAT- MEDLINE DCOM- 20200720 LR - 20211204 IS - 1558-2035 (Electronic) IS - 1558-2027 (Linking) VI - 21 IP - 1 DP - 2020 Jan TI - Effects of sacubutril/valsartan on nutritional status in heart failure with reduced ejection fraction. PG - 13-20 LID - 10.2459/JCM.0000000000000895 [doi] AB - BACKGROUND: Malnutrition commonly occurs in patients with heart failure with reduced ejection fraction (HFrEF). Sacubitril/valsartan, which is an AT1 neprilysin inhibitor, has been shown to reduce mortality and hospitalization in patients with HFrEF. However, its effects on nutritional status remain unclear. METHODS: Sacubitril/valsartan was initiated in 164 symptomatic patients with HFrEF receiving an optimal medical treatment with angiotensin inhibition (mean age: 63 +/- 20 years; 120 males, 60% ischemic cause). The New York Heart Association (NYHA) functional class and nutritional statuses of the patients were evaluated at the switching to AT1 neprilysin inhibitor and at the 6th-month follow-up of the maximum sacubitril/valsartan dose using the geriatric nutritional risk index (GNRI), controlling nutritional status (CONUT) score, prognostic nutritional index (PNI), and prealbumin. RESULTS: After the sacubutril/valsartan treatment, a significant reduction in the number (%) of malnourished patients was observed according to CONUT (before 47% vs. after 7%, P < 0.001), GNRI (before 39% vs. after 19%, P < 0.001), PNI scores (before 36% vs. after 12%, P = 0.002), and prealbumin (before 41% vs. after 12%, P < 0.001). Also significant changes were observed at the baseline and follow-up in the mean scores of the three different nutritional indexes and prealbumin levels [CONUT: 2.68 +/- 2.5, 1.02 +/- 1.0 (P < 0.001); GNRI: 97.1 +/- 9.7, 101.2 +/- 5.9 (P < 0.001); PNI: 38.8 +/- 4.8, 41.6 +/- 3.7 (P < 0.001); prealbumin: 14.6 +/- 6.9 mg/dl, 17.1 +/- 5.2 mg/dl (P < 0.001)]. Overall, the patients exhibited a significant functional improvement following the initiation of sacubitril/valsartan: 23% of the patients improved by two NYHA classes, 48% improved by one NYHA class, and 39% remained stable. CONCLUSION: In patients with HFrEF, the switch from angiotensin-converting enzyme inhibitor/angiotensin II receptor blocker therapy to sacubitril/valsartan resulted in a significant improvement in both nutritional and functional statuses. FAU - Dereli, Seckin AU - Dereli S AD - Department of Cardiology, Ordu State Hospital. FAU - Bayramoglu, Adil AU - Bayramoglu A AD - Deparment of Cardiology, Ordu University Faculty of Medicine, Ordu, Turkey. FAU - Kaya, Ahmet AU - Kaya A AD - Deparment of Cardiology, Ordu University Faculty of Medicine, Ordu, Turkey. LA - eng PT - Journal Article PL - United States TA - J Cardiovasc Med (Hagerstown) JT - Journal of cardiovascular medicine (Hagerstown, Md.) JID - 101259752 RN - 0 (Aminobutyrates) RN - 0 (Angiotensin II Type 1 Receptor Blockers) RN - 0 (Biphenyl Compounds) RN - 0 (Drug Combinations) RN - 0 (Protease Inhibitors) RN - 0 (Tetrazoles) RN - 80M03YXJ7I (Valsartan) RN - EC 3.4.24.11 (Neprilysin) RN - WB8FT61183 (sacubitril and valsartan sodium hydrate drug combination) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Aminobutyrates/adverse effects/*therapeutic use MH - Angiotensin II Type 1 Receptor Blockers/adverse effects/*therapeutic use MH - Biphenyl Compounds MH - Drug Combinations MH - Drug Substitution MH - Female MH - Heart Failure/diagnosis/*drug therapy/physiopathology MH - Humans MH - Male MH - Malnutrition/diagnosis/*drug therapy/physiopathology MH - Middle Aged MH - Neprilysin/antagonists & inhibitors MH - Nutrition Assessment MH - Nutritional Status/*drug effects MH - Prospective Studies MH - Protease Inhibitors/adverse effects/*therapeutic use MH - Recovery of Function MH - Stroke Volume/*drug effects MH - Tetrazoles/adverse effects/*therapeutic use MH - Time Factors MH - Treatment Outcome MH - Valsartan MH - Ventricular Function, Left/*drug effects EDAT- 2019/11/13 06:00 MHDA- 2020/07/21 06:00 CRDT- 2019/11/13 06:00 PHST- 2019/11/13 06:00 [pubmed] PHST- 2020/07/21 06:00 [medline] PHST- 2019/11/13 06:00 [entrez] AID - 01244665-202001000-00003 [pii] AID - 10.2459/JCM.0000000000000895 [doi] PST - ppublish SO - J Cardiovasc Med (Hagerstown). 2020 Jan;21(1):13-20. doi: 10.2459/JCM.0000000000000895.