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Effects of Ghrelin Treatment on Exercise Capacity in Underweight COPD Patients: a substudy of a multicenter, randomized, double-blind, placebo-controlled trial of ghrelin treatment
BMC Pulmonary Medicine volume 13, Article number: 37 (2013)
The aim of this substudy of the ghrelin treatment, multicenter, randomized, double-blind, placebo-controlled trial was to investigate the effects of ghrelin administration on exercise capacity and the underlying mechanisms in underweight patients with chronic obstructive pulmonary disease (COPD) using cardiopulmonary exercise testing.
Twenty underweight COPD patients were randomized to pulmonary rehabilitation with intravenous ghrelin (2 μg/kg, n = 10) or placebo (n = 10) twice daily for 3 weeks in a double-blind fashion. The primary outcome was changes in peak oxygen uptake . Secondary outcomes included changes in exertional cardio-respiratory functions: O2-pulse, physiologic dead space/tidal volume-ratio (VD/VT), ventilatory equivalent for oxygen , and ventilatory equivalent for carbon dioxide .
With incremental exercise, at peak exercise, there was a significant difference in the mean difference (ghrelin minus placebo), i.e., treatment effect in: i) peak (1.2 mL/kg/min, 95% CI: 0.2-2.3 mL/kg/min, between-group p = 0.025); ii) (-4.2, 95% CI: -7.9 to -0.5, between-group p = 0.030); iii) (-4.1, 95% CI: -8.2 to -0.1, between-group p = 0.045); iv) VD/VT (-0.04, 95% CI: -0.08 to -0.00, between-group p = 0.041); and v) O2-pulse (0.7 mL/beat, 95% CI: 0.3 to 1.2 mL/beat, between-group p = 0.003). Additionally, repeated-measures analysis of variance (ANOVA) indicated a significant time-course effect of ghrelin versus placebo in the peak (p = 0.025).
Ghrelin administration was associated with improved exertional capacity and improvements in ventilatory-cardiac parameters.
UMIN (University Hospital Medical Information Network in Japan) C000000061
Chronic obstructive pulmonary disease (COPD) is a major health issue, especially in its advanced stages. It is characterized by a significant systemic deterioration, so-called pulmonary cachexia, that affects exercise capacity, quality of life, and survival in such patients [1–6]. Treatment strategies targeting pulmonary cachexia have been attempted and have provided insight into the pathogenetic mechanisms of pulmonary cachexia [2, 7].
Pulmonary rehabilitation (PR) is recommended as a therapeutic strategy in many diseases, including cachectic COPD . However, it has been important to determine whether cachectic COPD patients are capable of adaptive responses to PR, because PR may partially disturb anabolic and catabolic balance in such patients [2, 9].
Ghrelin is an endogenous ligand for growth hormone (GH) secretagogue receptor (GHSR), originally isolated from the stomach . Given that ghrelin has GH-releasing activity, ghrelin may have beneficial effects in COPD patients through a GH-dependent mechanism. Meanwhile, as a GH-independent mechanism, ghrelin induces a positive energy balance by decreasing fat utilization , stimulating food intake and adiposity , increasing cardiac output in healthy humans , and inhibiting sympathetic nerve activity [13, 14]. In an open-label pilot study, we previously demonstrated that ghrelin may improve walking distance and inhibit sympathetic nerve activity in underweight COPD patients . More recently, a multicenter, randomized, double-blind, placebo-controlled trial was conducted to investigate the efficacy and safety of adding ghrelin to PR in underweight COPD patients, and it showed that ghrelin administration improved symptoms and respiratory muscle strength. While the results were considered most likely to have been due to ghrelin treatment, the precise mechanism that underlies the improvement of exercise performance or symptoms remains unclear. This study was simultaneously conducted in a single center as part of a multicenter, randomized, double-blind, placebo-controlled study of underweight COPD patients . The primary objective was to investigate whether ghrelin-PR combination treatment would improve exercise capacity. A secondary objective was to determine whether the underlying mechanisms of the improvements in response to ghrelin would be associated with improvement of exertional cardio-respiratory functions and attenuation of exertional sympathetic nervous system activity. Some results of this trial have been reported in abstract form .
The eligibility criteria for participation were as follows: 1) moderate to severe COPD (FEV1% of less than 70% and % forced expiratory volume in one second (FEV1) 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 if they met any of the following: 1) malignant tumors; 2) active infection; 3) severe heart disease; 4) hepatic dysfunction (serum levels of aspartate aminotransferase and alanine aminotransferase twice the upper limit of normal or more); 5) asthma; 6) definitely or possibly pregnant; 7) change in drug regimen within 4 weeks before participation in this study; or 8) judged to be unable to participate in this study by their physician, in addition to the above exclusion criteria.
This study was a 3-week, randomized, double-blind, placebo-controlled trial of ghrelin administration during PR conducted at a single center (Toneyama National Hospital) as part of a main multicenter trial . To test the primary hypothesis that ghrelin-PR combination treatment would improve exercise capacity, recruitment was from September 2005 until the target sample size of 18 was achieved on May 2009.
This study was approved by the ethics committee of the National Hospital Organization Toneyama National Hospital (approval number, 0311) and was conducted according to the Declaration of Helsinki and Good Clinical Practice guidelines. Written informed consent was obtained from all subjects (in Japanese). Enrolled patients were randomly assigned in a 1:1 ratio to receive 3-week PR with either ghrelin or placebo in a double-blind fashion (Figure 1). 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 daily for 3 weeks in hospital. Randomization was done in our center considered as a block in the main multicenter study . 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. The test drug controller managed a copy of the randomization list and the test drugs at the pharmacy department of the National Hospital Organization Toneyama National Hospital. At study completion, the randomization list was used to confirm appropriate conduct of the trial. Patients were tested at pre-treatment and post-treatment, i.e., Week 3. The main multicenter study , including this study, is registered at https://upload.umin.ac.jp/cgi-open-bin/ctr/ctr.cgi?function=brows&action=brows&type=summary&recptno=R000000103&language=E, number C000000061.
Preparation of human ghrelin
Human ghrelin was prepared as described previously [15, 16]. In brief, ghrelin was stored in 2-mL volumes, each containing 120 μg ghrelin. The chemical nature and content of the human ghrelin in vials were confirmed as described previously [15, 16]. All vials were stored frozen at -30°C until the time of preparation for administration.
Pulmonary rehabilitation (PR)
Aerobic exercise training included in the PR program was conducted for 5 days per week, for 3 weeks, at high-intensity targets . The PR program consisted of disease education and instruction of patients and their families, physical therapy, i.e., conditioning including breathing control techniques, and aerobic exercise training. Occupational therapy was not included in the present PR program. The aerobic exercise training sessions were conducted as three sets (with 10-min breaks) daily, 5 days per week, for 3 weeks, and they were performed on electromechanically braked cycle ergometers. The initial exercise level of each set was set for 6 min at the work rate corresponding to 60% of the peak attained on baseline cardiopulmonary exercise testing (CPET). As tolerated by the subject, the exercise duration was initially increased to 10 min. After that, the training work rate was increased by 5 W, and then extended to the work rate corresponding to 80% of the baseline peak . If the subject found the set intolerable, it was reduced to its previous setting. Supplemental oxygen was used if necessary to maintain an oxygen saturation >90% during exercise training.
The primary outcome was change in exercise capacity, i.e., peak oxygen uptake . Secondary outcomes were changes in exertional dyspnea and plasma norepinephrine levels, as well as exertional cardio-respiratory functions: O2-pulse ( i.e., the product of stroke volume and the arterial-mixed venous O2 difference), physiologic dead space/tidal volume ratio (VD/VT, i.e., the degree of mismatching of ventilation to perfusion), ventilatory equivalent for oxygen ( , i.e., measurement of the ventilatory requirement for the metabolic rate), ventilatory equivalent for carbon dioxide (, i.e., measurement of the ventilatory requirement for the metabolic rate), and inspiratory capacity (IC).
Pulmonary function measurements were done as previously described . Symptom-limited exercise tests were conducted on an electrically-braked cycle ergometer (CV-1000SS, Lode, Groningen, The Netherlands) using a cardiopulmonary exercise testing (CPET) system (Vmaxs-29C, CareFusion 207, Palm Springs, CA, USA) . Incremental testing was performed, which consisted of 2-min increments to 10 W. Subsequent constant-load testing, which was conducted at 70% of the maximal incremental work rate obtained in pre-treatment, was performed to measure the exertional inspiratory capacity (IC) at pre-treatment and post-treatment with the same work rate. CPET was performed under room air conditions until subject exhaustion. Expired gas data were measured breath-by-breath and collected as 30-s averages at rest, during exercise at 2-min intervals, and at end-exercise. In addition, dyspnea and leg fatigue intensity (Borg scale) were evaluated, and arterial blood was collected at rest and during the last 15 s of each exercise stage and at end-exercise. Arterial blood samples for blood gas analyses, plasma norepinephrine, and plasma lactate were obtained and measured as previously described . Before ghrelin administration, blood samples were also collected after 30 min of bed rest in the morning following an overnight fast for measurement of plasma acyl-ghrelin by radioimmunoassay, as previously described .
Dual-Energy X-ray Absorptiometry (DEXA)
Dual energy x-ray absorptiometry (DEXA) was performed to assess total body composition, including lean body mass before and after ghrelin or placebo administration with PR, as previously described .
Respiratory and peripheral muscle strength
The maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) were measured, as described previously .
The main multicenter study’s target sample size was 60 in the original protocol at the time of study design . Before the main multicenter study ended, the power and sample size calculations were repeated using the estimated effect of only ghrelin treatment for improving 6-min walk distance (6-MWD), which was based on information from the pilot study [15, 16]. The recalculated sample size was 18 in the main multicenter trial. What constituted a clinically important change in peak after ghrelin treatment with PR was not known before the study ended. Therefore, a formal power calculation could not be done. As an exploratory study, it was confirmed that the number of patients that had completed the study in our center exceeded the number necessary for the re-calculated sample size of 18, though the calculation was not based on the primary outcome in the present study.
Two measurement points were used for evaluations of exercise parameters: iso-time and peak exercise point. “iso-time” was defined as the highest equivalent exercise time achieved during the CPETs performed at pre-treatment and Week 3 by a given subject. To obtain “iso-time” during exercise, the values of the cardio-respiratory parameters were calculated by linear interpolation between adjacent measurement points for each subject [20, 21]. The absolute values of the cardio-respiratory parameters were obtained during CPET at 2-min intervals, and at end-exercise.
All data are expressed as means ± SD unless otherwise indicated. Comparisons of baseline characteristics between the groups were made by Fisher’s exact tests and Wilcoxon rank sum tests. Effects were examined once, at Week 3 soon after 3-week treatment. The results at Week 3 were compared with the pre-treatment results 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 were also analyzed using repeated-measures analysis of variance (ANOVA). Spearman’s rank correlation coefficients were used to assess the relationships between the increase in the peak and other measurements. The statistical analysis of the present study was performed by Mr. K. Tsuguchi (Nihon Ultmarc Inc. Tokyo, Japan) who had no relevant conflicts of interest. A p value <0.05 was considered significant (SAS 9.1.3, SAS Institute Inc., Cary, NC, USA).
A total of 20 underweight patients (mean BMI (SD), 18.3 (2.3) kg/m2) was randomized to ghrelin treatment with PR (ghrelin group; n = 10) or placebo treatment with PR (placebo group; n = 10), and all patients completed the study protocol. There were no significant differences in baseline characteristics between the two groups (Table 1). No significant difference in the total work performed during 3-week PR (mean ± SD: ghrelin group, 6970 ± 6169 watt·min versus placebo group, 7167 ± 4310 watt·min, between-group p = 0.935) was observed. Next, the effects of ghrelin administration on exercise capacity, as well as the underlying mechanisms were examined once (Week 3) using two measurement points: iso-time and the peak exercise point.
Peak incremental exercise responses
The distribution of reasons for stopping exercise was not different after ghrelin than after placebo; most subjects in both groups stopped primarily because of dyspnea or a combination of dyspnea and leg discomfort (ghrelin group, 80% versus placebo group, 60%), and fewer subjects stopped because of leg discomfort (ghrelin group, 20% versus placebo group, 40%). The ghrelin-PR combination substantially increased the peak (mean difference (ghrelin minus placebo), i.e., treatment effect = 1.2 mL/kg/min, 95% CI: 0.2 to 2.3 mL/kg/min, between-group p = 0.025, Table 2 and Figure 2A, or as an alternative description, treatment effect = 60.5 mL/kg, 95% CI: 10.5 to 110.5 mL/kg, between-group p = 0.020). Additionally, repeated-measures analysis of variance (ANOVA) indicated a significant time-course effect of ghrelin versus placebo in the peak (p = 0.025). After ghrelin-PR combination treatment, the peak increased by >2 mL/kg/min in two patients and decreased in none. Furthermore, compared with placebo, the ghrelin-PR combination significantly increased (treatment effect = 0.7 mL/beat, 95% CI: 0.3 to 1.2 mL/beat, between-group p = 0.003) and decreased VD/VT (treatment effect = -0.04, 95% CI: -0.08 to -0.00, between-group: p = 0.041), (treatment effect = -4.1, 95% CI: -8.2 to -0.1, between-group: p = 0.045), and (treatment effect = -4.2, 95% CI: -7.9 to -0.5, between-group: p = 0.030), but maintained the dyspnea rating unchanged (Table 2 and Figure 2B-2D).
Iso-time responses with incremental exercise
The ghrelin-PR combination significantly decreased the dyspnea score from baseline, but not compared to placebo (Table 3). The ghrelin-PR combination decreased VD/VT compared to placebo (treatment effect = -0.04, 95% CI: -0.08 to -0.00, between-group p = 0.048) and (within group: p < 0.05), and increased VT (within-group: p < 0.01), with a resultant decrease in the respiratory frequency (f) (within-group p < 0.05) (Table 3). The ghrelin-PR combination did not inhibit plasma norepinephrine levels.
The responses on dynamic hyperinflation with constant load exercise
The ghrelin-PR combination significantly increased IC at the iso-time point (within-group p < 0.05) and peak exercise (within-group p < 0.05), though the treatment effect compared with placebo was not significant.
Correlates of improvement
The intra-subject increase in the peak after ghrelin treatment correlated with the plasma acyl-ghrelin level after treatment (r = -0.797, p = 0.006), which in turn correlated with the increase induced by treatment in the plasma acyl-ghrelin level (r = -0.684, p = 0.029) and minute ventilation (r = 0.657, p = 0.039).
This substudy of a multicenter, randomized, double-blind, placebo-controlled trial of ghrelin treatment in underweight COPD patients was designed and powered to investigate the effects of repeated ghrelin administration and the underlying mechanisms using cardiopulmonary exercise testing. The main findings were as follows. 1) With incremental exercise, in the ghrelin group, the mean change from pre-treatment i) in peak was significantly increased compared with the placebo group, and ii) that in dyspnea intensity showed a significant within-group decrease at the iso-time point. Furthermore, iii) the mean changes from pre-treatment in , , and VD/VT were significantly improved compared with the placebo group at peak exercise; iv) the mean change from pre-treatment in VT showed a significant within-group increase at peak exercise; and v) that in O2-pulse was increased compared with the placebo group at peak exercise. 2) With constant-load exercise, in the ghrelin group, the mean change from pre-treatment in IC showed a significant within-group increase throughout exercise.
Many approaches to treating cachectic COPD have been attempted [2, 7]. In the present study, exercise training alone did not show significant improvements in exertional capacity and cardio-ventilatory parameters, except for endurance time. In the placebo group, (mean difference: -0.8 mL/kg/min, within-group: p = 0.051) and O2-pulse were not improved at the iso-time point (Table 3). The plasma norepinephrine levels seemed to be inhibited at the iso-time point (Table 3). Given the reported negative connotations of sympathetic activation in cardiac as well as respiratory disease patients [22–26], sympathetic inhibition may have positive consequences in COPD. These findings suggest that underweight patients with COPD who undergo exercise training can only increase their endurance time, efficiently decreasing and plasma norepinephrine levels. In contrast, repeated ghrelin administration was associated with a significant increase from pre-treatment in the peak by an average of 1.4 mL/kg/min (between-group p = 0.025, Table 2 and Figure 2A). Endurance time was not increased after ghrelin-PR combination treatment (Table 2). These findings suggest that patients treated with ghrelin had a high exercise capacity with instantaneous force, though the pedal revolutions per minute on the electrically braked-cycle ergometer were not monitored. We considered the following potential mechanisms for the increase in exercise capacity that was induced by ghrelin treatment: i) improved ventilatory efficiency and ventilatory volume; and ii) increased cardiac function.
The two major contributing factors leading to exercise limitation in COPD may be the increased ventilatory requirement and the decreased ventilatory capacity . In the ghrelin group, VD/VT, , and , which are useful to estimate wasted ventilation, were significantly decreased at peak exercise (Table 2, Figure 2B and C), resulting in a decreased ventilatory requirement. These findings suggest that ghrelin treatment was associated with an improvement of ventilatory efficiency at peak exercise. VT during incremental exercise (Tables 2 and 3) and IC during constant-load exercise were increased after ghrelin-PR combination treatment, though the difference compared with placebo was not significant. Additionally, increased peak after ghrelin treatment was positively correlated with the change in from pre-treatment. In the present study, 4 weeks after the completion of ghrelin and PR treatment, MEP was better in the ghrelin group than in the placebo group (Table 4). These findings suggest that these improvements in ventilatory parameters may occur through the mechanism by which ghrelin improved respiratory muscle strength . On the other hand, ghrelin may have additional beneficial effects within the cardiovascular system in underweight COPD patients. Earlier studies showed that ghrelin improved cardiac function in normal subjects and in patients/animals with heart failure [13, 28, 29]. In the ghrelin group, the O2-pulse after treatment increased significantly compared with placebo at peak incremental exercise. Furthermore, a recent study demonstrated that ghrelin acts on the central nervous system to attenuate sympathetic nervous activity , though in the present study, as well as in the main study, ghrelin treatment did not show significant sympathetic inhibition compared with placebo. Further studies are needed to confirm the clinical significance such as regulating exertional dyspnea. Nevertheless, we believe that these improvements in cardio-ventilatory parameters could represent the effect of ghrelin.
It should be noted that individuals in this study had different reactions to PR or ghrelin therapy. Of note, in the present study, the exercise capacity improvement by exogenous ghrelin was negatively correlated with the increase in the plasma acyl-ghrelin level after treatment (r = -0.684). Since the half-life of exogenous ghrelin, which was administered on the day before blood sampling, was about 20 min , it is highly possible that the measured plasma acyl-ghrelin level was unaffected by the administered exogenous ghrelin, and reflected the endogenous acyl-ghrelin. These correlations may stand to reason, given that ghrelin administration is considered as replacement therapy for underweight COPD patients who may be unable to compensate for the anabolic-catabolic imbalance, resulting in increasing the endogenous plasma acyl-ghrelin levels, thought repeated exogenous ghrelin might inhibit ghrelin production . Meanwhile, as an effective adjunctive therapy, we used exercise training as a part of PR, which is well accepted to improve exercise performance [8, 32]. However, it is important to determine whether PR improves or worsens it, especially in underweight patients in the severe disease stage.
This study had some limitations. First, the number of participants was small, and few women were included in this trial. Given the exploratory nature of the present study, a formal power calculation was not possible. Many statistical comparisons under exercise conditions might increase the chance of type I error. As a consequence, the present findings should be considered preliminary and need to be confirmed in a future large study. Second, ghrelin did not show any effects on whole lean body mass and weight. The training work rate remained at the initial setting in 4 patients (40%) in each group during this trial, because they found the initial training work rate intolerable. The lack of response to exercise training or ghrelin treatment in weight and whole lean body mass may be related to the inability to tolerate the type, the intensity, and/or the duration of the exercise training. Third, there was a significant difference between the ghrelin and placebo groups in the peak measured by the protocol of 2-min increments to 10 W in the present study. However, in the main multicenter trial at Week 3, outcome measurements measured with a continuous ramp rate of 5 W/min showed no improvements with ghrelin compared to placebo . In the present study, in the ghrelin group, the mean change from pre-treatment in the peak measured by the protocol of 2-min increments to 10 W was larger than that measured by the protocol with the ramp rate of 5 W/min (mean difference: by 2-min increments to 10 W, 1.4 mL/kg/min versus with a ramp rate of 5 W/min, 1.1 mL/kg/min). See Table E1 in Additional file 2 (Supplementary Results) for other details. Several investigators have suggested the desirability of adjusting the work rate increment in exercise testing according to the patient’s cardiopulmonary condition [33, 34]. Tests in which the work rate increased too rapidly may not allow sufficient data for the evaluation to be accumulated. A more suitable exercise testing protocol, considering the patient’s cardiopulmonary condition, should have been conducted in the main multicenter trial. Also, in the present study, at Week 7, i.e., 4 weeks after the completion of the treatment, CPET should have been conducted to evaluate the sustained effects of ghrelin treatment, as shown in the multicenter trial .
Given the short-term nature of the study and the discrepancy between the physiological findings and the measures of direct patients benefit, the present findings need to be confirmed by further study. However, in the present substudy, ghrelin administration was associated with improved exertional capacity and improvements in cardio-ventilatory parameters, although the main multicenter study showed no significant difference between the ghrelin and placebo group in exercise capacity. Development of ghrelin administration as a novel cachexia-targeted therapy capable of improving exercise performance may be helpful in COPD treatment.
Body mass index
Chronic obstructive pulmonary disease
Cardiopulmonary exercise testing
Carbon monoxide diffusing capacity
Forced expiratory volume in one second
Forced vital capacity
long-acting muscarinic antagonist
plasma lactate level
Maximum voluntary ventilation
Plasma norepinephrine level
Arterial carbon dioxide tension
Arterial oxygen tension
Pulmonary function test
Short-acting muscarinic antagonist
Physiologic dead space/tidal volume ratio
Ventilatory equivalent for carbon dioxide
Ventilatory equivalent for oxygen
Wilson DO, Rogers RM, Wright EC, Anthonisen NR: Body weight in chronic obstructive pulmonary disease. The National Institutes of Health Intermittent Positive-Pressure Breathing Trial. Am Rev Respir Dis. 1989, 139 (6): 1435-1438. 10.1164/ajrccm/139.6.1435.
Wagner PD: Possible mechanisms underlying the development of cachexia in COPD. Eur Respir J. 2008, 31 (3): 492-501. 10.1183/09031936.00074807.
Schols AM, Slangen J, Volovics L, Wouters EF: Weight loss is a reversible factor in the prognosis of chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 1998, 157 (6 Pt 1): 1791-1797.
Schols AM, Broekhuizen R, Weling-Scheepers CA, Wouters EF: Body composition and mortality in chronic obstructive pulmonary disease. Am J Clin Nutr. 2005, 82 (1): 53-59.
Morley JE, Thomas DR, Wilson MM: Cachexia: pathophysiology and clinical relevance. Am J Clin Nutr. 2006, 83 (4): 735-743.
Landbo C, Prescott E, Lange P, Vestbo J, Almdal TP: Prognostic value of nutritional status in chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 1999, 160 (6): 1856-1861. 10.1164/ajrccm.160.6.9902115.
Burdet L, De Muralt B, Schutz Y, Pichard C, Fitting JW: Administration of growth hormone to underweight patients with chronic obstructive pulmonary disease. A prospective, randomized, controlled study. Am J Respir Crit Care Med. 1997, 156 (6): 1800-1806. 10.1164/ajrccm.156.6.9704142.
Zinna EM, Yarasheski KE: Exercise treatment to counteract protein wasting of chronic diseases. Curr Opin Clin Nutr Metab Care. 2003, 6 (1): 87-93. 10.1097/00075197-200301000-00013.
Laveneziana P, Palange P: Physical activity, nutritional status and systemic inflammation in COPD. Eur Respir J. 2012, 40 (3): 522-529. 10.1183/09031936.00041212.
Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, Kangawa K: Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature. 1999, 402 (6762): 656-660. 10.1038/45230.
Tschop M, Smiley DL, Heiman ML: Ghrelin induces adiposity in rodents. Nature. 2000, 407 (6806): 908-913. 10.1038/35038090.
Nakazato M, Murakami N, Date Y, Kojima M, Matsuo H, Kangawa K, Matsukura S: A role for ghrelin in the central regulation of feeding. Nature. 2001, 409 (6817): 194-198. 10.1038/35051587.
Nagaya N, Kojima M, Uematsu M, Yamagishi M, Hosoda H, Oya H, Hayashi Y, Kangawa K: Hemodynamic and hormonal effects of human ghrelin in healthy volunteers. Am J Physiol Regul Integr Comp Physiol. 2001, 280 (5): R1483-R1487.
Matsumura K, Tsuchihashi T, Fujii K, Abe I, Iida M: Central ghrelin modulates sympathetic activity in conscious rabbits. Hypertension. 2002, 40 (5): 694-699. 10.1161/01.HYP.0000035395.51441.10.
Nagaya N, Itoh T, Murakami S, Oya H, Uematsu M, Miyatake K, Kangawa K: Treatment of cachexia with ghrelin in patients with COPD. Chest. 2005, 128 (3): 1187-1193. 10.1378/chest.128.3.1187.
Miki K, Maekura R, Nagaya N, Nakazato M, Kimura H, Murakami S, Ohnishi S, Hiraga T, Miki M, Kitada S, et al: Ghrelin treatment of cachectic patients with chronic obstructive pulmonary disease: a multicenter, randomized, double-blind, placebo-controlled trial. PLoS One. 2012, 7 (5): e35708-10.1371/journal.pone.0035708.
Miki K, Maekura R, Hiraga T, Hashimoto H, Kitada S, Miki M, Yoshimura K, Tateishi Y, Motone M: Effects of ghrelin administration in cachectic patients with COPD. Eur RespirJ. 2010, 54 (36 Suppl): 335s-
Miki K, Maekura R, Hiraga T, Kitada S, Miki M, Yoshimura K, Tateishi Y: Effects of oxygen on exertional dyspnoea and exercise performance in patients with chronic obstructive pulmonary disease. Respirology. 2012, 17 (1): 149-154. 10.1111/j.1440-1843.2011.02086.x.
Itoh T, Nagaya N, Yoshikawa M, Fukuoka A, Takenaka H, Shimizu Y, Haruta Y, Oya H, Yamagishi M, Hosoda H, et al: Elevated plasma ghrelin level in underweight patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2004, 170 (8): 879-882. 10.1164/rccm.200310-1404OC.
O'Donnell DE, Chau LK, Webb KA: Qualitative aspects of exertional dyspnea in patients with interstitial lung disease. J Appl Physiol. 1998, 84 (6): 2000-2009.
Maltais F, Hamilton A, Marciniuk D, Hernandez P, Sciurba FC, Richter K, Kesten S, O'Donnell D: Improvements in symptom-limited exercise performance over 8 h with once-daily tiotropium in patients with COPD. Chest. 2005, 128 (3): 1168-1178. 10.1378/chest.128.3.1168.
Miki K, Maekura R, Hiraga T, Hashimoto H, Kitada S, Miki M, Yoshimura K, Tateishi Y, Sugano T, Motone M: Exertional dyspnea-related acidotic and sympathetic responses in patients with sequelae of pulmonary tuberculosis. J Physiol Sci. 2010, 60 (3): 187-193. 10.1007/s12576-009-0083-1.
Miki K, Maekura R, Hiraga T, Hashimoto H, Kitada S, Miki M, Yoshimura K, Tateishi Y, Fushitani K, Motone M: Acidosis and raised norepinephrine levels are associated with exercise dyspnoea in idiopathic pulmonary fibrosis. Respirology. 2009, 14 (7): 1020-1026. 10.1111/j.1440-1843.2009.01607.x.
Anker SD, Coats AJ: Cardiac cachexia: a syndrome with impaired survival and immune and neuroendocrine activation. Chest. 1999, 115 (3): 836-847. 10.1378/chest.115.3.836.
Anker SD, Chua TP, Ponikowski P, Harrington D, Swan JW, Kox WJ, Poole-Wilson PA, Coats AJ: Hormonal changes and catabolic/anabolic imbalance in chronic heart failure and their importance for cardiac cachexia. Circulation. 1997, 96 (2): 526-534. 10.1161/01.CIR.96.2.526.
Andreas S, Anker SD, Scanlon PD, Somers VK: Neurohumoral activation as a link to systemic manifestations of chronic lung disease. Chest. 2005, 128 (5): 3618-3624. 10.1378/chest.128.5.3618.
Wasserman K, Hansen JE, Sue DY, Stringer WW, Whipp BJ: Principles of exercise testing and interpretation. 2005, Philadelphia, PA: Lippincott, Williams and Wilkins, 111-132. 4
Nagaya N, Uematsu M, Kojima M, Ikeda Y, Yoshihara F, Shimizu W, Hosoda H, Hirota Y, Ishida H, Mori H, et al: Chronic administration of ghrelin improves left ventricular dysfunction and attenuates development of cardiac cachexia in rats with heart failure. Circulation. 2001, 104 (12): 1430-1435. 10.1161/hc3601.095575.
Nagaya N, Miyatake K, Uematsu M, Oya H, Shimizu W, Hosoda H, Kojima M, Nakanishi N, Mori H, Kangawa K: Hemodynamic, renal, and hormonal effects of ghrelin infusion in patients with chronic heart failure. J Clin Endocrinol Metab. 2001, 86 (12): 5854-5859. 10.1210/jc.86.12.5854.
Akamizu T, Takaya K, Irako T, Hosoda H, Teramukai S, Matsuyama A, Tada H, Miura K, Shimizu A, Fukushima M, et al: Pharmacokinetics, safety, and endocrine and appetite effects of ghrelin administration in young healthy subjects. Eur J Endocrinol. 2004, 150 (4): 447-455. 10.1530/eje.0.1500447.
Kojima M, Kangawa K: Ghrelin: structure and function. Physiol Rev. 2005, 85 (2): 495-522. 10.1152/physrev.00012.2004.
Casaburi R, Patessio A, Ioli F, Zanaboni S, Donner CF, Wasserman K: Reductions in exercise lactic acidosis and ventilation as a result of exercise training in patients with obstructive lung disease. Am Rev Respir Dis. 1991, 143 (1): 9-18. 10.1164/ajrccm/143.1.9.
Arstila M: Pulse-conducted triangular exercise-ECG test. A feed-back system regulating work during exercise. Acta Med Scand Suppl. 1972, 529: 3-109.
Redwood DR, Rosing DR, Goldstein RE, Beiser GD, Epstein SE: Importance of the design of an exercise protocol in the evaluation of patients with angina pectoris. Circulation. 1971, 43 (5): 618-628. 10.1161/01.CIR.43.5.618.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2466/13/37/prepub
Funding was received 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 authors would like to thank Dr. Y. Onishi (Non Profit Organization, Institute for Health Outcomes and Process Evaluation Research, Japan) for his help in calculating sample size, Mr. K. Tsuguchi (Nihon Ultmarc Inc. Tokyo, Japan) for performing the statistical analysis, Ms. Y. Tsuchie (Toneyama National Hospital) for her assistance with this study, and Mr. T. Uenishi (Toneyama National Hospital) for obtaining the CPET measurements. They authors would also like to thank the members of the main study that included this substudy at Miyazaki University School of Medicine (Prof. M. Nakazato, Dr. N. Matsumoto, and Dr. Y. Arimura), Nara Medical University (Prof. H. Kimura and Dr. M. Yoshikawa), and the National Cardiovascular Center Research Institute (Dr. K. Yamahara).
The authors declare that they have no competing interests.
KM, RM, NN, SK, M. Miki, KY, YT, M. Motone, TH, M. Mori, and KK conceived and designed the experiments. KM, RM, SK, M. Miki, KY, YT, M. Motone, TH, M. and Mori performed the experiments. KM, RM, NN, SK, M. Miki, KY, YT, M. Motone, TH, M. Mori, and KK analyzed the data. KM wrote the manuscript. All authors read and approved the final manuscript.
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Miki, K., Maekura, R., Nagaya, N. et al. Effects of Ghrelin Treatment on Exercise Capacity in Underweight COPD Patients: a substudy of a multicenter, randomized, double-blind, placebo-controlled trial of ghrelin treatment. BMC Pulm Med 13, 37 (2013) doi:10.1186/1471-2466-13-37
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