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.
In a multicenter, randomized, double-blind, placebo-controlled trial, 33 cachectic COPD patients were randomly assigned PR with intravenous ghrelin (2 µg/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.
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.
UMIN Clinical Trial Registry C000000061
Citation: Miki K, Maekura R, Nagaya N, Nakazato M, Kimura H, et al. (2012) Ghrelin Treatment of Cachectic Patients with Chronic Obstructive Pulmonary Disease: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial. PLoS ONE 7(5): e35708. doi:10.1371/journal.pone.0035708
Editor: Christian Taube, Leiden University Medical Center, The Netherlands
Received: December 9, 2011; Accepted: March 20, 2012; Published: May 1, 2012
Copyright: © 2012 Miki et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Funding was from the Research Grant from the Ministry of Health, Labour and Welfare in Japan; the Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation (NIBIO) of Japan; the Takeda Scientific Foundation in Japan; and Health and Labour Sciences Research Grants, Clinical Research, H20-translational research-general-002. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Pulmonary cachexia is common in the advanced stage of chronic obstructive pulmonary disease (COPD), and it is an independent risk factor for death in such patients , . Based on the notion that advanced COPD affects the whole body and causes wasting syndromes, many different therapeutic approaches have been attempted to improve this syndrome , .
Pulmonary rehabilitation (PR) including exercise training is well accepted to improve exercise performance and quality of life in COPD patients , and it has been regarded as a nutritional adjunct therapy .
During the 1970s and 1980s, many gut peptides were identified . Ghrelin, first discovered in 1999 as a novel growth hormone (GH)-releasing peptide isolated from the stomach, has been identified as an endogenous ligand for GH secretagogue receptor . Ghrelin also has a variety of GH-independent effects, such as causing a positive energy balance and weight gain by decreasing fat utilization , stimulating food intake , and inhibiting sympathetic nerve activity , . In addition, plasma ghrelin levels were elevated in cachectic COPD patients and were associated with the cachectic state and pulmonary function abnormalities, suggesting that endogenous ghrelin increased to compensate for the cachectic state and may provide important clues to improve the catabolic-anabolic imbalance in such patients. In an open-label pilot study, we showed that ghrelin treatment increased walking distance in cachectic COPD patients . Based on the above available evidence, a multicenter, randomized, double-blind, placebo-controlled study was conducted to test the hypothesis that the addition of ghrelin treatment to PR might benefit cachectic COPD patients. The objectives were to investigate the efficacy and safety of adding ghrelin to PR in cachectic COPD patients.
Study Design and Patients
The study was a 3-week, multicenter, randomized, double-blind, placebo-controlled trial of ghrelin administration during PR. The study was finally conducted at four clinical centers (National Cerebral and Cardiovascular Center, Miyazaki University School of Medicine, Nara Medical University, and National Hospital Organization Toneyama National Hospital) in Japan from September 2005 through May 2009, because Graduate School of Medicine, Osaka City University did not participate just before the start of the clinical trial. The study was conducted according to the Declaration of Helsinki and Good Clinical Practice guidelines and approved by the ethics committees of all participating study centers: The ethics committee of the National Cerebral and Cardiovascular Center (approval number, M17–13); The ethics committee of Miyazaki University School of Medicine (approval number, 218): The ethics committee of Nara Medical University (approval number, 05–012); and The ethics committee of the National Hospital Organization Toneyama National Hospital (approval number, 0311). All patients gave written informed consent (in Japanese). The inclusion criteria were as follows: 1) severe to very severe COPD (forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) of less than 70% and FEV1 percent predicted of less than 50%); 2) underweight (body mass index (BMI)<21 kg/m2); 3) clinically stable and able to participate in PR; 4) between 20 and 85 years old; and 5) signed the agreement for participation in this study. Participants were excluded for any of the following: 1) malignant tumors; 2) active infection; 3) severe heart disease; 4) hepatic dysfunction (serum aspartate aminotransferase and alanine aminotransferase levels at least twice the upper limit of normal); 5) renal dysfunction (serum creatinine levels ≥2.0 mg/dl); 6) asthma; 7) definitely or possibly pregnant; 8) change in drug regimen within 4 weeks before participation in this study; or 9) judged to be unable to participate in this study by their physician. This study was registered with UMIN (University Hospital Medical Information Network in Japan: http://www.umin.ac.jp/ctr/), number C000000061.
Randomization and Interventions
Randomization was done in each center considered as a block. The randomization list was generated by a statistician from Hamamatsu University School of Medicine and maintained there until the study was finished and unblinded. Neither the physicians nor the patients were aware of the treatment assignments. Patients who met the eligibility criteria were enrolled and randomly assigned in a 1:1 ratio to receive PR with either ghrelin (2 µg/kg) or placebo twice a day for 3 weeks in hospital. The administration of ghrelin (2 µg/kg, ghrelin solution with 10 ml saline) or placebo was done intravenously over 30 minutes at a constant rate and repeated twice a day for 3 weeks. Patients were tested at pre-treatment, Week 3 after start of ghrelin or placebo administration with PR, and Week 7 after start of ghrelin or placebo administration with PR, i.e., 4 weeks after the completion of the combination treatment (Figure 1).
Preparation of Human Ghrelin
Human ghrelin obtained from the Peptide Institute Inc. was dissolved in distilled water with 3.75% D-mannitol and sterilized as described previously . Ghrelin was stored in 2-ml volumes, each containing 120 µg ghrelin. The chemical nature and content of the human ghrelin in vials were rarefied as described previously . All vials were stored frozen at −30°C until the time of preparation for administration.
Exercise training, which was included in the PR program, was conducted in three sets daily, every weekday for 3 weeks (i.e. 15 days) at high-intensity targets. Additional details are described online in Supplementary Methods S1.
Efficacy: The primary outcomes were changes in 6-min walk distance (6-MWD) and the score evaluated using the St. George Respiratory Questionnaire (SGRQ) . Secondary outcomes were changes in the health-related QoL (HRQoL) score using the Short-Form 36 questionnaire (SF 36 v2™ Health Survey, Japanese version) , ,  and the Medical Research Council (MRC) dyspnea scale , peak oxygen uptake (), food intake, FEV1/FVC, vital capacity (VC), respiratory muscle strength, and plasma norepinephrine levels in the resting condition.
Safety: All randomized patients who received at least one dose of the study treatments (ghrelin group, n = 18; placebo group, n = 15) were included in the safety analyses using intention-to-treat analysis. Blood tests were done up to Week 7. All serious adverse events were monitored throughout the study period.
Open circles, ghrelin; closed circles, placebo. Data are presented as mean differences±SE. * p<0.05: change between pre- and post-treatment (within-group difference). † p<0.05: change between pre-treatment and post-treatment (between ghrelin and placebo group difference). ‡ p<0.05: time course effect of ghrelin versus placebo by repeated-measures ANOVA. A) In both groups, 6-MWD increases significantly to a similar level from pre-treatment at Week 3. Prolonged effects can be seen in the ghrelin group at Week 7, though the improvement in 6-MWD declined in the placebo group. B) Though the MRC score became progressively worse in the placebo group, the maintained effects in the MRC score can be seen in the ghrelin group at Week 7. C) Repeated-measures ANOVA indicated significant time course effects of ghrelin versus placebo in MEP (F (2, 51) = 4.17, p = 0.021).
6-min Walk Test
The 6-MWD was measured as described previously .
Cardiopulmonary Exercise Testing (CPET)
While breathing room air with a mask, symptom-limited CPET was conducted on an electrically braked cycle ergometer using an incremental protocol (continuous ramp rate of 5 W/min). Expired gas data were measured breath-by-breath and collected as 30-s averages at rest and during exercise. The CPET was done until subject exhaustion.
Food intake was assessed as described previously .
Respiratory and Peripheral Muscle Strength
The maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) were measured as described previously . Peripheral muscle strength was measured by the maximal voluntary handgrip maneuver as described previously .
Dual-Energy X-ray Absorptiometry (DEXA)
All participating centers measured dual energy x-ray absorptiometry (DEXA) to assess the total body composition, including lean body mass. The measurements were performed with the subject lying in a supine position. As a general rule, a single expert from each center analyzed the scans from the corresponding center.
Blood Samples and Analyses
Serum GH, serum insulin-like growth factor (IGF)-1, serum tumor necrosis factor α (TNF-α), serum interleukin-6 (IL-6), and plasma norepinephrine were measured as described previously . Additional details are described online in Supplementary Methods S1.
The study’s target accrual was 60 in the original protocol at the time of study design (see supporting information; Protocol S1). When 31 of the 33 randomized patients completed this study, we re-performed the power and sample size calculation, and confirmed that the number of patients that had completed the study exceeded the number necessary for the re-calculated sample size of 18. As a result, this trial ended prematurely. Because i) it is difficult to prolong hospitalization considering the current status of health care insurance in Japan, and ii) what constituted a clinically important change in 6-MWD after ghrelin treatment with PR was not known before the study ended; the sample size calculation was re-performed on the estimated effect of only ghrelin treatment for improving 6-MWD, which was based on information from the pilot study . The resultant total sample size of 18 was finally used to provide the power (80%) to detect a mean difference of 60 m in 6-MWD with an estimated SD of 40 m using a two-sided alpha of 0.05, though the study’s target accrual stated in the original protocol was 60.
Open circles, ghrelin; closed circles, placebo. Data are presented as mean differences±SE. * p<0.05: change between pre- and post-treatment (within-group difference). † p<0.05: change between pre-treatment and post-treatment (between ghrelin and placebo group difference). ‡ p<0.05: time course effect of ghrelin versus placebo by repeated-measures ANOVA. At Week 3, marked improvements in SGRQ scores are not seen in both groups. However, SGRQ scores, especially SGRQ symptom scores, are significantly improved in the ghrelin group at Week 7. B) Repeated-measures ANOVA indicated significant time course effects of ghrelin versus placebo in SGRQ symptoms (F (2, 51) = 3.19, p = 0.049).
All data are expressed as means±SD or SE unless otherwise indicated. Comparisons of baseline characteristics between the two groups were made by Fisher’s exact tests and Wilcoxon rank sum tests. Effects were examined once or twice; that is i) at Week 3 soon after 3-week treatment or ii) at Week 3 and Week 7 (i.e., 4 weeks after the completion of 3-week treatment). The results at Week 3 and Week 7, respectively, were compared with the pre-treatment within each group, and between the two groups using paired t-tests and unpaired t-tests, respectively. To assess the time course efficacy of ghrelin versus placebo, post-treatment data up to Week 7 were also assessed using a repeated-measures analysis of variance (ANOVA). A p value<0.05 was considered significant (SAS 9.1.3, SAS Institute Inc., Cary, NC, USA).
Of the 33 randomized patients, 31completed the 3-week study; 2 patients in the ghrelin group discontinued study medications due to pneumonia and depression, respectively. Of the 31 patients who completed the randomized 3-week study, in the ghrelin group, one patient had infective enteritis after 3 weeks of medications, and one had low back pain due to lumbar spondylosis before and throughout the 3 weeks of medications. Two patients in the placebo group were lost to follow-up after the Week 3 measurements. Therefore, 29 patients (ghrelin, n = 14; placebo, n = 15) were included in the study analyses to ensure adequate efficacy evaluation using pre-protocol analysis. The mean BMI in the enrolled patients (n = 29) was very low (mean±SD, 18.3±2.1 kg/m2). The treatment groups were generally well-matched with regard to demographics and baseline characteristics (Table 1).
At pre-treatment, compared with placebo, a single administration of ghrelin markedly increased serum GH levels from baseline (mean change±SE: ghrelin group 46.4±6.2 ng/ml at the mean peak time (35 min) versus the placebo group 1.1±0.5 ng/ml at the mean peak time (55 min); between group p<0.0001), the effect of which was maintained at Week 3 (mean change±SE: ghrelin group 15.8±2.1 ng/ml at the mean peak time (30 min) versus the placebo group 0.4±0.2 ng/ml at the mean peak time (65 min); between group p<0.0001). Three-week ghrelin-PR combination treatment tended to increase serum IGF-1 levels (mean change±SE: 12±6 ng/ml, within-group p = 0.093).
Exercise Tolerance and Gas Exchange Measurements
At both Week 3 and Week 7, there were no significant differences between the ghrelin and placebo groups in 6-MWD. In each group, at Week 3, a similar significant increase from pre-treatment in 6-MWD was observed (mean difference: ghrelin group +40 m, within group p = 0.033 versus placebo group +35 m, within group p = 0.013). The effect remained at Week 7 in the ghrelin group, whereas in the placebo group, the improvement in 6-MWD was reduced at Week 7 (mean difference: ghrelin group within group +47 m, p = 0.017 versus placebo group +18 m, within group p = 0.14) (Table 2 and Figure 2A). To assess the time course efficacy of ghrelin versus placebo in 6-MWD, a repeated-measures ANOVA was performed. There was no significant time course effect of ghrelin versus placebo in 6-MWD (F (2, 51) = 1.10, p = 0.34).
In the ghrelin group, the peak and /HR were significantly increased by 1.2 ml/kg/min and 0.5 ml/beats, respectively, from pre-treatment (within-group p = 0.021, p = 0.019, respectively) (Table 2). However, there was no significant difference between the two groups in the peak and /HR. In the ghrelin group, the ventilatory equivalents for oxygen (E/) was relatively improved by −3.9 from pre-treatment (within group p = 0.060).
HRQoL and MRC Measures
In both groups, there was no significant difference in each SGRQ score and MRC score between pre-treatment and at Week 3. At Week 7, there was a significant treatment effect between the two groups in SGRQ symptoms (between-group: p = 0.026, Table 3 and Figure 3B), and in the MRC score (between-group p = 0.030, Table 2 and Figure 2B). At Week 7, in the ghrelin group, SGRQ total was decreased by 6.0 from pre-treatment (within-group p = 0.046, between-group p = 0.072) (Table 3 and Figure 3A). Furthermore, there was a significant time course effect of ghrelin versus placebo in SGRQ symptoms (repeated-measures ANOVA, F (2, 51) = 3.19, p = 0.049, Figure 3B).
Body Weight and Food Intake
In the ghrelin group, at Week 1, the relative increase in body weight was+0.42 kg (within group p = 0.092), which was reduced by Week 3 and followed by a re-increase at Week 7 (+0.8 kg, within group: p = 0.054). However there was no significant difference in body weight between the groups at each Week (Table 2). No affect on whole lean body mass from ghrelin was seen at Week 3 (Table 2). No significant increase from baseline in food intake was observed at Week 3 in both groups (Table 2).
Respiratory and Peripheral Muscle Strength
In the ghrelin group, at Week 3, the post-treatment increase in respiratory muscle strength, as indicated by MEP and MIP, was not significantly different from that in the placebo group, but at Week 7, the mean increase from pre-treatment in MEP (+15.6 cmH2O) was significantly different from that in the placebo group (between group p = 0.015) (Table 2). Furthermore, there was a significant time course effect of ghrelin versus placebo in MEP (repeated-measures ANOVA, F (2, 51) = 4.17, p = 0.021, Figure 2C).
At Week 3 and Week 7, there was no significant treatment effect between the two groups in grip strength (Table 2).
Pulmonary Function, Plasma Norepinephrine, and Other Hormone Levels
Ghrelin treatment did not significantly change any parameters of the pulmonary function tests, serum TNF-α, serum IL-6, or plasma norepinephrine at rest (Table 2).
Throughout this trial, 67% of patients in the ghrelin group and 33% of patients in the placebo group reported 12 and 5 adverse events, respectively, but there was no significant difference between the groups (Table 4). In the ghrelin group, alanine aminotransferase increased to 41 IU/L in one patient (6%), and total cholesterol increased to 270 mg/dl in one patient (6%); both increases disappeared at Week 7. Two patients randomized to ghrelin discontinued as a result of adverse events: one because of bacterial pneumonia, and one because of depression, both of which were not considered related to ghrelin treatment. One patient randomized to ghrelin developed lung cancer 2 years and 9 months after the end of ghrelin administration, but this was judged by the efficacy and safety committee as not causally related to ghrelin treatment, considering the period of disease development and the incidence rate of lung cancer .
The present study is the first multicenter, randomized, double-blind, placebo-controlled study to assess the effect and safety of repeated ghrelin administration to very severe cachectic patients with COPD. The main results of this study can be summarized as follows. In the ghrelin group, single administration of ghrelin was accompanied by a significant increase in serum GH levels during 3-week treatment, and there was no significant difference in 6-MWD between ghrelin and placebo at Week 3 and at Week 7. With ghrelin, symptomatic improvements in SGRQ symptoms and MRC score were not obtained at Week 3, but significant differences between ghrelin and placebo were seen at Week 7. In the ghrelin group, no significant within-group improvement from pre-treatment was seen in respiratory muscle strength, as indicated by MEP and MIP, at Week 3, but there was a significant difference in MEP between ghrelin and placebo at Week 7. Repeated-measures ANOVA showed significant time course effects of ghrelin versus placebo in SGRQ symptoms and MEP. Finally, ghrelin treatment was well tolerated.
Ghrelin treatment may have beneficial, continuing effects after treatment on HRQoL and MRC measures in this population. Though this study was conducted to determine the effectiveness of ghrelin in cachectic COPD patients, considering a synergistic interaction between ghrelin and PR, the data of this study need to be interpreted with caution, because, especially in advanced stage patients, excessive exercise training may partially worsen the anabolic and catabolic balance , . In the present study, which included patients with a lower exercise capacity and pulmonary function than those in the pilot study  and more cachectic patients than those in other studies on PR , the 6-MWD after 3-week PR in the placebo group was decreased in 3 (20%) of the 15 patients. Since 5 patients (33%) in the placebo group found the initial training work rate intolerable, the initial training work rate remained at its initial setting. In addition, at Week 3, outcome measurements showed no improvements with ghrelin compared with placebo. These findings may represent patients’ variable responses to PR, which might have an influence on the effects of ghrelin. Of note, however, there were significant treatment effects of ghrelin in both SGRQ symptoms and MRC score. In addition, the treatment tended to improve the total SGRQ score by more than 4 points; a clinically meaningful improvement. These effects were not observed soon after the 3 week-treatment, but were seen 4 weeks after treatment, maintaining the improvement obtained in 6-MWD at Week 3. Similarly, 4 weeks after treatment, the effect of ghrelin on respiratory muscle strength was confirmed, though it has been reported that GH alone does not increase strength in healthy elderly , , . Furthermore, repeated-measures ANOVA indicated significant time course effects of ghrelin versus placebo in SGRQ symptoms and MEP. Our data suggest that improving of the respiratory muscle strength, the O2 pulse, and the ventilatory equivalents for oxygen may serve as a mechanism by which ghrelin-PR combination treatment improved symptoms, though further examination is needed to understand the precise mechanism. These findings suggest that repeated ghrelin administration may have beneficial, sustained effects after administration on symptoms through GH-dependent and/or -independent mechanisms.
Cachectic elderly patients with COPD who were given intravenous ghrelin showed a continuous increase of pulsatile GH secretion in the present study. There is evidence that insufficiency of sarcopenia-related hormones, such as GH and IGF-1, may contribute to cachexia , . Observational studies in cachectic COPD patients have found decreased levels of these hormones , . In the present study, despite significant increases in GH secretion levels throughout the 3-week treatment and respiratory muscle strength, ghrelin provided only a significant within-group increase in exercise performance, and a relative within-group increase in IGF-1 levels and body weight. Furthermore, ghrelin did not affect food intake, grip strength or plasma norepinephrine levels at rest in the present study. Although DEXA should be performed a greater number of times during the trial, at Week 3 ghrelin did not show any effects on whole lean body mass. Meanwhile, previous studies showed that ghrelin administration induced a positive energy balance and weight gain , increased food intake , , and decreased sympathetic nervous activity , , . The discrepancy may be explained by the fact that the intensity of exercise training for some cachectic participants counteracted the effects of ghrelin, though lower extremity exercise training at higher intensity produces greater benefits than lower intensity training . As one of the reasons, the patients treated with both ghrelin and exercise training gained at Week 1, which was not seen in the placebo group. However, this weight gain reduced by Week 3. At Week 7, the weight was regained (Table 2). The days of attending PR in the ghrelin group was negatively correlated with the increase in body weight from Week 3 to Week 7 (r = −0.710, p = 0.003). We speculate that the unintended excessive exercise permitted by ghrelin administration with antidepressant-like effects  might prevent the obtained results. Nevertheless, these findings suggest that clinical interventions with ghrelin may help cachectic COPD patients via inhibiting somatopause and regulating metabolic balance.
The participants in the present study tolerated daily administration of ghrelin for 3 weeks (Table 4); the most frequent ghrelin-related side effects were mild and similar to those of previous reports , , , as well as with those of GH administration by injection . However, given that the previous studies of the responses of ghrelin in proliferation, including tumor development, have demonstrated conflicting findings , , , , more studies of the safety of ghrelin treatment are necessary before clinical application.
This study had some limitations. First, the number of participants was small, and few females were included in this trial. Second, the duration of the study was short. A more effective exercise training program, considering its intensity and frequencies, should have been conducted. Additional studies are needed to evaluate a more suitable regimen of ghrelin-PR.
In conclusion, ghrelin administration provided sustained improvements in symptoms and respiratory strength in cachectic COPD patients. Development of ghrelin administration methods may offer potential advantages over the currently approved treatment options for COPD. The lack of a significant between-group difference in exercise tolerance may result from the exercise training program conducted as the combination therapy. Careful examination is needed to develop more effective administration methods of ghrelin and combination therapy with ghrelin.
The authors are particularly grateful to the patients who agreed to participate. The authors would also like to thank Dr. Yoshihiro Onishi (Institute for Health Outcomes and Process Evaluation Research, Japan) for his help in calculating sample size, Mr. Kazunori Tsuguchi (Nihon Ultmarc Inc. Japan) for performing the statistical analysis, and other members of Ghrelin Study Group as follows:
Junichi Ashitani, (Faculty of Medicine, University of Miyazaki, Department of Neurology, Respirology, Endocrinology and Metabolism, Internal Medicine); Atsuhiko Fukuoka, (Nara Medical University, Second Department of Internal Medicine); Yukio Fujita (Nara Medical University, Second Department of Internal Medicine);Yoshifumi Yamamoto, (Nara Medical University, Second Department of Internal Medicine); Hisako Hashimoto, (National Hospital Organization (NHO), Toneyama National Hospital, Department of Internal Medicine); Motone Masaharu (NHO, Toneyama National Hospital, Department of Internal Medicine); Norifumi Nakanishi, (National Cerebral and Cardiovascular Center (NCVC), Department of Cardiovascular Medicine); Hideo Oya, (NCVC, Department of Cardiovascular Medicine); Kohichi Tanaka, (NCVC, Research Institute, Department of Regenerative Medicine & Tissue Engineering); Hiroaki Naito, (NCVC, Department of Radiology and Nuclear Medicine); Sakashita Yoshiharu (NCVC, Department of Radiology and Nuclear Medicine); Takeshi Kotake, (NCVC, Department of Pharmacy); Hideki Morishita, (NCVC, Department of Pharmacy); Mitsuyoshi Nakashima, (Hamamatsu University School of Medicine); Hitonobu Tomoike, (NCVC); Kentaro Kimura, (NHO Kinki-Chuo Chest Medical Center, Clinical Research Center); Naotsugu Kurihara, (Ikuwakai Memorial Hospital, Department of Respiratory Medicine); Yukio Nagasaka, (Sakai Hospital Kinki University Faculty of Medicine, Department of Respiratory Medicine); Hisayuki Matsuo, (NCVC, Research Institute).
Conceived and designed the experiments: NN KK MN HK RM MY KM SM SO NM K. Yamahara. Performed the experiments: RM KM HK MN NN TH MM SK K. Yoshimura YT MY SM YA NM SO. Analyzed the data: KM RM HK MN NN TH MM SK K. Yoshimura YT MY SM YA NM SO K. Yamahara KK. Wrote the paper: KM.
- 1. Wagner PD (2008) Possible mechanisms underlying the development of cachexia in COPD. Eur Respir J 31: 492–501.
- 2. Wilson DO, Rogers RM, Wright EC, Anthonisen NR (1989) Body weight in chronic obstructive pulmonary disease. The National Institutes of Health Intermittent Positive-Pressure Breathing Trial. Am Rev Respir Dis 139: 1435–1438.
- 3. Burdet L, de Muralt B, Schutz Y, Pichard C, Fitting JW (1997) Administration of growth hormone to underweight patients with chronic obstructive pulmonary disease. A prospective, randomized, controlled study. Am J Respir Crit Care Med 156: 1800–1806.
- 4. Ries AL, Bauldoff GS, Carlin BW, Casaburi R, Emery CF, et al. (2007) Pulmonary Rehabilitation: Joint ACCP/AACVPR Evidence-Based Clinical Practice Guidelines. Chest 131: 4S–42S.
- 5. Zinna EM, Yarasheski KE (2003) Exercise treatment to counteract protein wasting of chronic diseases. Curr Opin Clin Nutr Metab Care 6: 87–93.
- 6. Zaloga GP (2005) Ghrelin, diet, and pulmonary function. Chest 128: 1084–1086.
- 7. Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, et al. (1999) Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature 402: 656–660.
- 8. Tschop M, Smiley DL, Heiman ML (2000) Ghrelin induces adiposity in rodents. Nature 407: 908–913.
- 9. Nakazato M, Murakami N, Date Y, Kojima M, Matsuo H, et al. (2001) A role for ghrelin in the central regulation of feeding. Nature 409: 194–198.
- 10. Matsumura K, Tsuchihashi T, Fujii K, Abe I, Iida M (2002) Central ghrelin modulates sympathetic activity in conscious rabbits. Hypertension 40: 694–699.
- 11. Nagaya N, Kojima M, Uematsu M, Yamagishi M, Hosoda H, et al. (2001) Hemodynamic and hormonal effects of human ghrelin in healthy volunteers. Am J Physiol Regul Integr Comp Physiol 280: R1483–1487.
- 12. Itoh T, Nagaya N, Yoshikawa M, Fukuoka A, Takenaka H, et al. (2004) Elevated plasma ghrelin level in underweight patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 170: 879–882.
- 13. Nagaya N, Itoh T, Murakami S, Oya H, Uematsu M, et al. (2005) Treatment of cachexia with ghrelin in patients with COPD. Chest 128: 1187–1193.
- 14. Jones PW, Quirk FH, Baveystock CM, Littlejohns P (1992) A self-complete measure of health status for chronic airflow limitation. The St. George’s Respiratory Questionnaire. Am Rev Respir Dis 145: 1321–1327.
- 15. Ware JE Jr, Sherbourne CD (1992) The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care 30: 473–483.
- 16. Fukuhara S, Bito S, Green J, Hsiao A, Kurokawa K (1998) Translation, adaptation, and validation of the SF-36 Health Survey for use in Japan. J Clin Epidemiol 51: 1037–1044.
- 17. Fukuhara S, Ware JE Jr, Kosinski M, Wada S, Gandek B (1998) Psychometric and clinical tests of validity of the Japanese SF-36 Health Survey. J Clin Epidemiol 51: 1045–1053.
- 18. Fletcher CM, Elmes PC, Fairbairn AS, Wood CH (1959) The significance of respiratory symptoms and the diagnosis of chronic bronchitis in a working population. Br Med J 2: 257–266.
- 19. Calverley PM, Spencer S, Willits L, Burge PS, Jones PW (2003) Withdrawal from treatment as an outcome in the ISOLDE study of COPD. Chest 124: 1350–1356.
- 20. Rabinovich RA, Ardite E, Mayer AM, Polo MF, Vilaro J, et al. (2006) Training depletes muscle glutathione in patients with chronic obstructive pulmonary disease and low body mass index. Respiration 73: 757–761.
- 21. Puhan MA, Schunemann HJ, Frey M, Scharplatz M, Bachmann LM (2005) How should COPD patients exercise during respiratory rehabilitation? Comparison of exercise modalities and intensities to treat skeletal muscle dysfunction. Thorax 60: 367–375.
- 22. Liu H, Bravata DM, Olkin I, Nayak S, Roberts B, et al. (2007) Systematic review: the safety and efficacy of growth hormone in the healthy elderly. Ann Intern Med 146: 104–115.
- 23. Papadakis MA, Grady D, Black D, Tierney MJ, Gooding GA, et al. (1996) Growth hormone replacement in healthy older men improves body composition but not functional ability. Ann Intern Med 124: 708–716.
- 24. Blackman MR, Sorkin JD, Munzer T, Bellantoni MF, Busby-Whitehead J, et al. (2002) Growth hormone and sex steroid administration in healthy aged women and men: a randomized controlled trial. JAMA 288: 2282–2292.
- 25. Anawalt BD, Merriam GR (2001) Neuroendocrine aging in men. Andropause and somatopause. Endocrinol Metab Clin North Am 30: 647–669.
- 26. Lamberts SW, van den Beld AW, van der Lely AJ (1997) The endocrinology of aging. Science 278: 419–424.
- 27. Creutzberg EC, Wouters EF, Mostert R, Pluymers RJ, Schols AM (2003) A role for anabolic steroids in the rehabilitation of patients with COPD? A double-blind, placebo-controlled, randomized trial. Chest 124: 1733–1742.
- 28. Koehler F, Doehner W, Hoernig S, Witt C, Anker SD, et al. (2007) Anorexia in chronic obstructive pulmonary disease–association to cachexia and hormonal derangement. Int J Cardiol 119: 83–89.
- 29. Lutter M, Elmquist J (2009) Depression and metabolism: linking changes in leptin and ghrelin to mood. F1000 Biol Rep 1:
- 30. Akamizu T, Takaya K, Irako T, Hosoda H, Teramukai S, et al. (2004) Pharmacokinetics, safety, and endocrine and appetite effects of ghrelin administration in young healthy subjects. Eur J Endocrinol 150: 447–455.
- 31. Nagaya N, Moriya J, Yasumura Y, Uematsu M, Ono F, et al. (2004) Effects of ghrelin administration on left ventricular function, exercise capacity, and muscle wasting in patients with chronic heart failure. Circulation 110: 3674–3679.
- 32. Cassoni P, Allia E, Marrocco T, Ghe C, Ghigo E, et al. (2006) Ghrelin and cortistatin in lung cancer: expression of peptides and related receptors in human primary tumors and in vitro effect on the H345 small cell carcinoma cell line. J Endocrinol Invest 29: 781–790.
- 33. Belloni AS, Macchi C, Rebuffat P, Conconi MT, Malendowicz LK, et al. (2004) Effect of ghrelin on the apoptotic deletion rate of different types of cells cultured in vitro. Int J Mol Med 14: 165–167.
- 34. Ghe C, Cassoni P, Catapano F, Marrocco T, Deghenghi R, et al. (2002) The antiproliferative effect of synthetic peptidyl GH secretagogues in human CALU-1 lung carcinoma cells. Endocrinology 143: 484–491.
- 35. Murata M, Okimura Y, Iida K, Matsumoto M, Sowa H, et al. (2002) Ghrelin modulates the downstream molecules of insulin signaling in hepatoma cells. J Biol Chem 277: 5667–5674.