Refrence | Author, years | Country | Type of study | Study subject | Sample size | Dose | Intervention group | Control group | Rout of administration | Mean age of participant | Out come | Intervention duration | Result | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Group | Mean ± SD change | Significance | SMD | |||||||||||||
26 | Bakalar et al. 2006 | The Czech Republic | RCT | Multiple-trauma patients | I = 20 P = 20 | 0.4 g/kg | MT | Placebo | PN | 30 | FBS | 8 days | I P | − 0.4 ± 1.6 1 ± 2.3 | No | − 0.71 |
26 | Bakalar et al. 2006 | The Czech Republic | RCT | Multiple-trauma patients | I = 20 P = 20 | 0.4 g/kg | MT | Placebo | PN | 30 | IS | 8 days | I P | 1.7 ± 5.8 4.5 ± 4.2 | Yes | − 0.55 |
29 | Mansour et al. 2015 | Iran | RCT | Patients with type 2 diabetes | I = 27 P = 26 | 30 g/day | MT | Placebo | Oral | 50 | FBS | 6 weeks | I P | –0.79 ± 1.35 –0.06 ± 1.70 | No | − 0.47 |
29 | Mansour et al. 2015 | Iran | RCT | Patients with type 2 diabetes | I = 27 P = 26 | 30 g/day | MT | Placebo | Oral | 50 | Insulin | 6 weeks | I P | 6.05 ± 14.1 1.67 ± 7.6 | No | 0.39 |
29 | Mansour et al. 2015 | Iran | RCT | Patients with type 2 diabetes | I = 27 P = 26 | 30 g/day | MT | Placebo | Oral | 50 | HbA1c | 6 weeks | I P | 0.17 ± 1.32 0.24 ± 1.68 | Yes | − 0.04 |
29 | Mansour et al. 2015 | Iran | RCT | Patients with type 2 diabetes | I = 27 P = 26 | 30 g/day | MT | Placebo | Oral | 50 | HOMA-IR | 6 weeks | I P | 0.52 ± 6.8 0.59 ± 2.5 | No | − 0.01 |
29 | Mansour et al. 2015 | Iran | RCT | Patients with type 2 diabetes | I = 27 P = 26 | 30 g/day | MT | Placebo | Oral | 50 | QUICKI | 6 weeks | I P | − 0.01 ± 0.05 − 0.01 ± 0.03 | No | 0 |
3 | Dock-Nascimento et al. 2012 | Brazil | RCT | Patients candidate for elective laparoscopic cholecystectomy | I = 9 P = 9 | 50 gr | CT | Placebo | Oral | 40 | FBS | 24 h | I P | 19.2 ± 6 38 ± 4 | YES | − 3.69 |
3 | Dock-Nascimento et al. 2012 | Brazil | RCT | Patients candidate for elective laparoscopic cholecystectomy | I = 9 P = 9 | 50 gr | CT | Placebo | Oral | 40 | Insulin | 24 h | I P | − 1.5 ± 0.8 1 ± 3.5 | No | − 0.99 |
3 | Dock-Nascimento et al. 2012 | Brazil | RCT | Patients candidate for elective laparoscopic cholecystectomy | I = 9 P = 9 | 50 gr | CT | Placebo | Oral | 40 | QUICKI | 24 h | I P | 0 ± 0.05 − 0.02 ± 0.02 | No | 0.52 |
27 | Cui et al. 2013 | China | RCT | Patients undergoing colonic cancer resection | I = 20 P = 20 | 0.5 g/kg | CT | Placebo | PN | 55 | FBS | 24 h | I P | 0.77 ± 1 1.17 ± 1.1 | Yes | − 0.38 |
27 | Cui et al. 2013 | China | RCT | Patients undergoing colonic cancer resection | I = 20 P = 20 | 0.5 g/kg | CT | Placebo | PN | 55 | Insulin | 24 h | I P | 0.19 ± 2.5 8.81 ± 3.1 | Yes | − 3.06 |
27 | Cui et al. 2013 | China | RCT | Patients undergoing colonic cancer resection | I = 20 P = 20 | 0.5 g/kg | CT | Placebo | PN | 55 | HOMA-IR | 24 h | I P | − 0.6 ± 0.6 2.3 ± 0.5 | No | − 5.23 |
27 | Cui et al. 2013 | China | RCT | Patients undergoing colonic cancer resection | I = 20 P = 20 | 0.5 g/kg | CT | Placebo | PN | 55 | QUICKI | 24 h | I P | − 0.03 ± 0.2 − 0.12 ± 0.2 | No | 0.45 |
23 | Singh et al. 2015 | India | RCT | Patients undergoing maxillofacial surgery | I = 5 P = 5 | 0.77 g/kg | CT | Placebo | Oral | 24 | FBS | 10 h | I P | 14.3 ± 15.1 35.3 ± 30.8 | No | − 0.87 |
23 | Singh et al. 2015 | India | RCT | Patients undergoing maxillofacial surgery | I = 5 P = 5 | 0.77 g/kg | CT | Placebo | Oral | 24 | Insulin | 10 h | I P | − 5.8 ± 2.1 − 1.4 ± 3.6 | No | − 1.5 |
23 | Singh et al. 2015 | India | RCT | Patients undergoing maxillofacial surgery | I = 5 P = 5 | 0.77 g/kg | CT | Placebo | Oral | 24 | HOMA-IR | 10 h | I P | − 1.2 ± 0.6 0.2 ± 0.8 | Yes | − 1.98 |
25 | Letellier et al. 2013 | France | Cross-over | Children with Duchenne muscular dystrophy | I = 30 P = 30 | 0.5 g/kg | MT | Placebo | Oral | 10 | FBS | 120 days | I P | 0 ± 0.22 0.08 ± 0.26 | Yes | − 0.33 |
25 | Letellier et al. 2013 | France | Cross-over | Children with Duchenne muscular dystrophy | I = 30 P = 30 | 0.5 g/kg | MT | Placebo | Oral | 10 | Insulin | 120 days | I P | 0.5 ± 0.97 0.22 ± 0.44 | No | 0.37 |
25 | Letellier et al. 2013 | France | Cross-over | Children with Duchenne muscular dystrophy | I = 30 P = 30 | 0.5 g/kg | MT | Placebo | Oral | 10 | HOMA-IR | 120 days | I P | 0.11 ± 0.27 0.001 ± 0.22 | No | 0.44 |
24 | Laviano et al. 2014 | Italy | RCT | Obese patients | I = 6 P = 6 | 0.5 g/kg | MT | Placebo | Oral | 43 | FBS | 28 days | I P | − 1.6 ± 8.7 0.2 ± 8.5 | No | − 0.21 |
24 | LaviaNo et al. 2014 | Italy | RCT | Obese patients | I = 6 P = 6 | 0.5 g/kg | MT | Placebo | Oral | 43 | Insulin | 28 days | I P | − 1.5 ± 4.1 0 ± 3.2 | No | − 0.4 |
24 | Laviano 2014 | Italy | RCT | Obese patients | I = 6 P = 6 | 0.5 g/kg | MT | Placebo | Oral | 43 | HOMA-IR | 28 days | I P | − 0.41 ± 0.7 0.2 ± 1.2 | No | − 0.62 |
28 | Hissa et al. 2011 | Brazil | RCT | Patients with coronary obstruction | I = 11 P = 11 | 0.19/Kg/h | CT | Placebo | PN | 63 | FBS | 1 day | I P | 35 ± 6.5 50 ± 7 | Yes | − 2.22 |
28 | Hissa et al. 2011 | Brazil | RCT | Patients with coronary obstruction | I = 11 P = 11 | 0.19/Kg/h | CT | Placebo | PN | 63 | Insulin | 1 day | I P | 20 ± 38.6 40 ± 50.8 | No | − 0.44 |
30 | Lomivorotov et al. 2012 | Russia | RCT | DM2 with coronary artery bypass graft surgery | I = 32 P = 32 | 0.4 g/kg/day | MT | Placebo | PN | 60 | FBS | 1 day | I P | 4.9 ± 1.65 3.7 ± 1.35 | No | 0.8 |
TG | ||||||||||||||||
23 | Singh et al. 2015 | India | Experimental | Patients undergoing maxillofacial surgery | I = 5 P = 5 | 0.77 g/kg | CT | Placebo | Oral | 24 | TG | 10 h | I P | − 17.6 ± 46.5 − 14.8 ± 13.8 | No | − 0.08 |
30 | Lomivorotov et al. 2012 | Russia | RCT | DM2 with coronary artery bypass graft surgery | I = 32 P = 32 | 0.4 g/kg/day | MT | Placebo | PN | 60 | TG | 1 | I P | − 1 ± 1.2 − 0.95 ± 0.4 | No | − 0.05 |
29 | Mansour et al. 2015 | Iran | RCT | Patients with type 2 diabetes | I = 27 P = 26 | 30 g/day | MT | Placebo | Oral | 50 | TG | 6 weeks | I P | –10.15 ± 60.1 3.69 ± 92.8 | No | − 0.18 |
Inflammatory markers | ||||||||||||||||
3 | Dock-Nascimento et al. 2012 | Brazil | RCT | Patients candidate for elective laparoscopic cholecystectomy | I = 9 P = 9 | 50 gr/day | CT | Placebo | Oral | 40 | CRP | 1 day | I P | 0.5 ± 0.5 0.7 ± 0.3 | Yes | − 0.48 |
3 | Dock-Nascimento et al. 2012 | Brazil | RCT | Patients candidate for elective laparoscopic cholecystectomy | I = 9 P = 9 | 50 gr/day | CT | Placebo | Oral | 40 | IL-6 | 1 day | I P | 2 ± 1.5 2.2 ± 0.7 | No | − 0.17 |
3 | Dock-Nascimento et al. 2012 | Brazil | RCT | Patients candidate for elective laparoscopic cholecystectomy | I = 9 P = 9 | 50 gr/day | CT | Placebo | Oral | 40 | GSH | 1 day | I P | 1 ± 3 2 ± 3 | No | − 0.33 |
31 | Engel et al. 2009 | Germany | RCT | Patients with cardiopulmonary bypass | I = 31 P = 20 | 0.5 mg/kg/day | MT | Placebo | PN | 71 | CRP | 3 days | I P | − 2 ± 15 8 ± 19 | No | − 0.58 |
31 | Engel et al. 2009 | Germany | RCT | Patients with cardiopulmonary bypass | I = 31 P = 20 | 0.5 mg/kg/day | MT | Placebo | PN | 71 | IL-6 | 3 days | I P | 1 ± 2.3 0.8 ± 2.5 | No | 0.08 |
31 | Engel et al. 2009 | Germany | RCT | Patients with cardiopulmonary bypass | I = 31 P = 20 | 0.5 mg/kg/day | MT | Placebo | PN | 71 | IL-1 | 3 days | I P | − 0.3 ± 3.1 0.3 ± 3.4 | No | − 0.18 |
31 | Engel et al. 2009 | Germany | RCT | Patients with cardiopulmonary bypass | I = 31 P = 20 | 0.5 mg/kg/day | MT | Placebo | PN | 71 | TNF-a | 3 days | I P | 1 ± 24 1 ± 24 | No | 0 |
31 | Engel et al. 2009 | Germany | RCT | Patients with cardiopulmonary bypass | I = 31 P = 20 | 0.5 mg/kg/day | MT | Placebo | PN | 71 | IL-8 | 3 days | I P | 1.1 ± 4.9 1 ± 2.5 | No | 0.02 |
33 | Ockenga 2002 | Germany | RCT | Patients with acute pancreatitis | I = 14 P = 14 | 0.3 g/kg/day | MT | Placebo | Oral | 53 | CRP | 14 days | I P | − 65 ± 60 − 21 ± 79 | Yes | − 0.63 |
32 | Cavalcante et al. 2012 | Brazil | RCT | Patients with systemic inflammatory response syndrome | I = 15 P = 15 | 30gr/day | MT | Placebo | Oral | 61 | IL-6 | 2 days | I P | 9.49 ± 30.3 − 12.27 ± 25.5 | No | 0.77 |
32 | Cavalcante et al. 2012 | Brazil | RCT | Patients with systemic inflammatory response syndrome | I = 15 P = 15 | 30gr/day | MT | Placebo | Oral | 61 | IL-1 | 2 days | I P | − 0.39 ± 0.5 0.07 ± 0.35 | No | -1.06 |
32 | Cavalcante et al. 2012 | Brazil | RCT | Patients with systemic inflammatory response syndrome | I = 15 P = 15 | 30gr/day | MT | Placebo | Oral | 61 | TNF-a | 2 days | I P | 0.18 ± 0.35 − 0.03 ± 0.38 | No | 0.57 |
32 | Cavalcante et al. 2012 | Brazil | RCT | Patients with systemic inflammatory response syndrome | I = 15 P = 15 | 30gr/day | MT | Placebo | Oral | 61 | GSH | 2 days | I P | − 18.9 ± 162.5 − 34.9 ± 160.8 | No | 0.09 |