| Literature DB >> 31019148 |
Takuro Okamura1, Yoshitaka Hashimoto1, Akane Miki1, Ayumi Kaji1, Ryosuke Sakai1, Keiko Iwai1, Takafumi Osaka1, Noriyuki Kitagawa2, Emi Ushigome1, Masahide Hamaguchi1,2, Mai Asano1, Masahiro Yamazaki1, Michiaki Fukui1.
Abstract
Association between heart failure and sarcopenia has been reported, however, the association between sarcopenia and brain natriuretic peptide (BNP) is unclear. Thus, we investigated the association between sarcopenia and BNP in type 2 diabetic patients without heart failure. In this cross-sectional study, skeletal muscle mass index (SMI, kg/m2) was calculated as appendicular muscle mass, measured by bioimpedance analyzer, by the square of the height. Sarcopenia was defined as having both handgrip strength of <26 kg for men and <18 kg for women, and SMI of <7.0 kg/m2 for men and <5.7 kg/m2 for women. To investigate the impact of BNP levels on the presence of sarcopenia, propensity-score matching analysis was used to remove the bias of confounding variables, including age, sex, duration of diabetes, body mass index, exercise, systolic blood pressure, smoking status, hemoglobin A1c, creatinine, energy and protein intake. The area under the curve (AUC) of BNP levels for the presence of sarcopenia was calculated by the receiver operating characteristic curve (ROC). Among 433 patients (236 men and 65.4 (11.1) years), 32 patients (7.4%) were diagnosed as sarcopenia. In the propensity-matched 58 patients, BNP levels (Δ10 pg/mL incremental) were associated with the presence of sarcopenia by logistic regression analysis, (odds ratio: 1.56, 95% confidence interval: 1.14-2.13, p = 0.002). The optimal cut-off point of BNP levels for sarcopenia is 27.3 pg/mL (AUC 0.777, 95%CI, 0.691-0.863, sensitivity = 0.813, specificity = 0.736, p < 0.001). In conclusion, BNP levels were associated with sarcopenia in type 2 diabetic patients without heart failure.Entities:
Keywords: Brain natriuretic peptide; Muscle mass; Nutrition; Sarcopenia; Type 2 diabetes
Year: 2019 PMID: 31019148 DOI: 10.1507/endocrj.EJ19-0024
Source DB: PubMed Journal: Endocr J ISSN: 0918-8959 Impact factor: 2.349