TY - JOUR
T1 - The effects of melatonin supplementation on inflammatory markers among patients with metabolic syndrome or related disorders
T2 - a systematic review and meta-analysis of randomized controlled trials
AU - Akbari, Maryam
AU - Ostadmohammadi, Vahidreza
AU - Tabrizi, Reza
AU - Lankarani, Kamran B.
AU - Heydari, Seyed Taghi
AU - Amirani, Elaheh
AU - Reiter, Russel J.
AU - Asemi, Zatollah
N1 - Funding Information:
Funding The research grant (no. 97-01-106-17191) was provided by Research Deputy of Shiraz University of Medical Sciences (SUMS).
Publisher Copyright:
© 2018, Springer International Publishing AG, part of Springer Nature.
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Objective: This systematic review and meta-analysis of randomized controlled trials (RCTs) was carried out to determine the effect of melatonin supplementation on the inflammatory markers among individuals with metabolic syndrome (MetS) and related disorders. Methods: We searched the following databases up to March 2018: PubMed, MEDLINE, EMBASE, Web of Science, and Cochrane Central Register of Controlled Trials. Three reviewers independently assessed study eligibility, extracted data, and evaluated risk of bias of included primary studies. Statistical heterogeneity was assessed using Cochran’s Q test and I-square (I2) statistic. Data were pooled using the random effect model and standardized mean difference (SMD) was considered as the summary effect size. Results: Six trials of 317 potential reports were identified to be suitable for our meta-analysis. The pooled results using random effects model indicated that melatonin supplementation significantly reduced C-reactive protein (CRP) (SMD = − 1.80; 95% CI − 3.27, − 0.32; P = 0.01; I2: 95.2) and interleukin 6 (IL-6) concentrations (SMD = − 2.02; 95% CI − 3.57, − 0.47; P = 0.01; I2: 91.2) among patients with MetS and related disorders; however, it did not affect tumor necrosis factor-α (TNF-α) concentrations (SMD = − 1.87; 95% CI − 3.81, 0.07; P = 0.05; I2: 94.4). Conclusions: In summary, the current meta-analysis showed the promising effect of melatonin administration on reducing CRP and IL-6, but not TNF-α levels among patients with MetS and related disorders. Additional prospective studies are recommended using higher supplementation doses and longer intervention period.
AB - Objective: This systematic review and meta-analysis of randomized controlled trials (RCTs) was carried out to determine the effect of melatonin supplementation on the inflammatory markers among individuals with metabolic syndrome (MetS) and related disorders. Methods: We searched the following databases up to March 2018: PubMed, MEDLINE, EMBASE, Web of Science, and Cochrane Central Register of Controlled Trials. Three reviewers independently assessed study eligibility, extracted data, and evaluated risk of bias of included primary studies. Statistical heterogeneity was assessed using Cochran’s Q test and I-square (I2) statistic. Data were pooled using the random effect model and standardized mean difference (SMD) was considered as the summary effect size. Results: Six trials of 317 potential reports were identified to be suitable for our meta-analysis. The pooled results using random effects model indicated that melatonin supplementation significantly reduced C-reactive protein (CRP) (SMD = − 1.80; 95% CI − 3.27, − 0.32; P = 0.01; I2: 95.2) and interleukin 6 (IL-6) concentrations (SMD = − 2.02; 95% CI − 3.57, − 0.47; P = 0.01; I2: 91.2) among patients with MetS and related disorders; however, it did not affect tumor necrosis factor-α (TNF-α) concentrations (SMD = − 1.87; 95% CI − 3.81, 0.07; P = 0.05; I2: 94.4). Conclusions: In summary, the current meta-analysis showed the promising effect of melatonin administration on reducing CRP and IL-6, but not TNF-α levels among patients with MetS and related disorders. Additional prospective studies are recommended using higher supplementation doses and longer intervention period.
KW - Inflammatory markers
KW - Melatonin
KW - Meta-analysis
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U2 - 10.1007/s10787-018-0508-7
DO - 10.1007/s10787-018-0508-7
M3 - Review article
C2 - 29907916
AN - SCOPUS:85048543345
VL - 26
SP - 899
EP - 907
JO - Inflammopharmacology
JF - Inflammopharmacology
SN - 0925-4692
IS - 4
ER -