Population | Baseline mean total testosterone (nmol/L) | |||||||
---|---|---|---|---|---|---|---|---|
Study identification | Country | Sample size | Major inclusion criteria | Major exclusion criteria | Sex (M/W) | Mean age (years) | Treated | Controls |
Casaburi et al37 | USA | 47 | Stable COPD, spirometry FEV1 ≤60% predicted and FEV1/VC ≤60%; total testosterone ≤13.9 nmol/L | CVD, low or high bodyweight, prostatic indications, haemoglobin ≥16 g/dL, orthopaedic impairments | M | 67 | (a) 10.5; (b) 14.1 | (a) 10.5; (b) 9.6 |
Creutzberg et al38 | The Netherlands | 56 | Stable COPD, ATS criteria, spirometry FEV1 <70% predicted and increase in FEV1 <10% postbronchodilation | Obesity, malignancies, CVD, gastrointestinal inflammatory disorders, type 1 diabetes, oxygen dependency at rest | M | 66 | 13.4 | 14.6 |
Ferreira et al39 | Brazil | 17 | Ambulatory and stable COPD, spirometry maximal inspiratory pressure <60% predicted and BMI <20 kg/m2 | CVD, prostatic indications | M | 69 | 14.4 | 17.2 |
Pison et al16 | France | 122 | Stable CRF, >18 years, PaO2 ≤8 kPa, long-term oxygen therapy and/or home mechanical ventilation >3 months, BMI ≤21 kg/m2 or fat-free mass index <25th centile | Pulmonary hypertension, sleep apnoea, prostatic indications, neuromuscular diseases, cystic fibrosis, conditions compromising 6-month survival, hormone-dependent cancer, women of childbearing age, elevated aminotransferase | M/W | 66 | M 12.7; W 0.45 | M 13.6; W 0.42 |
Sharma et al40 | Canada | 16 | Stable COPD, GOLD criteria stage 3–4, spirometry FEV1 <50% predicted and FEV1/FVC <0.7 | History of asthma, obesity, malignancy, CVD, prostatic indications, renal, hepatic, gastrointestinal or endocrine disease, recent surgery ≤2 months | M/W | 68 | M NR | W NR |
Svartberg et al41 | Norway | 29 | Stable COPD, moderate to severe, spirometry FEV1 <60% predicted | Asthma, malignancies, CVD, hepatic or endocrine disease | M | 66 | 21.6 | 20.5 |
Treatments | Control conditions | Trial duration (weeks) | Outcomes (assessments, units) | Quality score (out of 8) |
---|---|---|---|---|
(a) Testosterone enanthate, 100 mg/week IM; (b) Testosterone enanthate, 100 mg/week IM with RT | (a) Placebo; (b) Placebo with RT | 10 | Muscle strength (leg press, 1RM kg); cardiorespiratory fitness (bicycle, peak VO2 L/min and peak workload Watts) | 5.0 |
Nandrolone decanoate, 50 mg/2 weeks IM | Placebo | 8 | Muscle strength (knee extension, peak isometric force Newtons); cardiorespiratory fitness (bicycle, peak workload Watts and peak VO2 mL/min); HRQoL (SGRQ total score) | 6.0 |
Testosterone, 250 mg IM at baseline and oral stanozolol, 12 mg/day with PR | Placebo with PR 9–27 weeks | 27 | Cardiorespiratory fitness (bicycle, peak VO2% predicted; 6MWT, distance metres) | 5.0 |
Oral testosterone undecanoate, M 80 mg/W 40 mg twice daily with PR | Home education on self-management of COPD-related stress and anxiety | 13 | Muscle strength (knee extension, peak isometric force Newtons); cardiorespiratory fitness (6MWT, distance metres; bicycle, peak workload Watts); HRQoL (CRQ total score) | 5.0 |
Nandrolone decanoate, M 50 mg/W 25 mg/2 weeks IM with PR | Placebo with PR | 16 | Muscle strength (knee extension, peak isometric force units NR); cardiorespiratory fitness (bicycle, peak VO2% predicted and peak workload Watts; 6MWT, distance metres); HRQoL (CRQ fatigue subscore) | 4.5 |
Testosterone enanthate, 250 mg/4 weeks IM | Placebo | 26 | Cardiorespiratory fitness (6MWT, distance metres) | 5.5 |
1RM, one repetition maximum; 6MWT, 6 min walking test; ATS, American Thoracic Society; BMI, body mass index; COPD, chronic obstructive pulmonary disease; CRF, chronic respiratory failure; CRQ, chronic respiratory questionnaire; CVD, cardiovascular diseases; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; GOLD, Global Initiative for Chronic Obstructive Lung Disease; HRQoL, health-related quality of life; IM, intramuscular injection; M, men; NR, not reported; PR, pulmonary rehabilitation; RT, resistance training; VO2, volume of oxygen uptake; W, women.