Ghrelin Treatment of Cachectic Patients with Chronic Obstructive Pulmonary Disease: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial

被引:95
作者
Miki, Keisuke [1 ]
Maekura, Ryoji [1 ]
Nagaya, Noritoshi [2 ]
Nakazato, Masamitsu [3 ]
Kimura, Hiroshi [4 ]
Murakami, Shinsuke [4 ]
Ohnishi, Shunsuke [2 ]
Hiraga, Toru [1 ]
Miki, Mari [1 ]
Kitada, Seigo [1 ]
Yoshimura, Kenji [1 ]
Tateishi, Yoshitaka [1 ]
Arimura, Yasuji [3 ]
Matsumoto, Nobuhiro [3 ]
Yoshikawa, Masanori [4 ]
Yamahara, Kenichi [2 ]
Kangawa, Kenji [5 ]
机构
[1] Toneyama Natl Hosp, Natl Hosp Org, Dept Internal Med, Toyonaka, Osaka, Japan
[2] Natl Cerebral & Cardiovasc Ctr, Res Inst, Dept Regenerat Med, Suita, Osaka, Japan
[3] Miyazaki Univ, Fac Med, Dept Neurol Respirol Endocrinol & Metab, Miyazaki, Japan
[4] Nara Med Univ, Dept Internal Med 2, Kashihara, Nara 634, Japan
[5] Natl Cerebral & Cardiovasc Ctr, Res Inst, Dept Biochem, Suita, Osaka, Japan
关键词
GROWTH-HORMONE; UNDERWEIGHT PATIENTS; HEALTH SURVEY; CACHEXIA; EXERCISE; SF-36; MEN; REHABILITATION; SAFETY;
D O I
10.1371/journal.pone.0035708
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Pulmonary cachexia is common in advanced chronic obstructive pulmonary disease (COPD), culminating in exercise intolerance and a poor prognosis. Ghrelin is a novel growth hormone (GH)-releasing peptide with GH-independent effects. The efficacy and safety of adding ghrelin to pulmonary rehabilitation (PR) in cachectic COPD patients were investigated. Methodology/Principal Findings: In a multicenter, randomized, double-blind, placebo-controlled trial, 33 cachectic COPD patients were randomly assigned PR with intravenous ghrelin (2 mg/kg) or placebo twice daily for 3 weeks in hospital. The primary outcomes were changes in 6-min walk distance (6-MWD) and the St. George Respiratory Questionnaire (SGRQ) score. Secondary outcomes included changes in the Medical Research Council (MRC) scale, and respiratory muscle strength. At pre-treatment, serum GH levels were increased from baseline levels by a single dose of ghrelin (mean change, +46.5 ng/ml; between-group p<0.0001), the effect of which continued during the 3-week treatment. In the ghrelin group, the mean change from pre-treatment in 6-MWD was improved at Week 3 (+40 m, within-group p = 0.033) and was maintained at Week 7 (+47 m, within-group p = 0.017), although the difference between ghrelin and placebo was not significant. At Week 7, the mean changes in SGRQ symptoms (between-group p = 0.026), in MRC (between-group p = 0.030), and in maximal expiratory pressure (MEP; between-group p = 0.015) were better in the ghrelin group than in the placebo group. Additionally, repeated-measures analysis of variance (ANOVA) indicated significant time course effects of ghrelin versus placebo in SGRQ symptoms (p = 0.049) and MEP (p = 0.021). Ghrelin treatment was well tolerated. Conclusions/Significance: In cachectic COPD patients, with the safety profile, ghrelin administration provided improvements in symptoms and respiratory strength, despite the lack of a significant between-group difference in 6-MWD.
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页数:10
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