Balasubramanian Haribalakrishna, Patole Sanjay
Haribalakrishna Balasubramanian, Sanjay Patole, Department of Neonatal Paediatrics, KEM Hospital for Women, Subiaco, Perth WA 6008, Australia.
World J Methodol. 2015 Sep 26;5(3):157-63. doi: 10.5662/wjm.v5.i3.157.
To conduct a systematic review of studies on early probiotic supplementation to prevent childhood metabolic syndrome (MS).
Using the Cochrane systematic review strategy we searched PubMed, EMBASE, CENTRAL, CINAHL, and the conference proceedings of the Pediatric American Society meetings and trial registries in December 2014. Randomised controlled trials (RCTs) and non RCTs of probiotic supplementation to the mother and/or infant for a minimum duration of 4 wk were selected. Of these, studies that reported on MS or its components (obesity, raised blood pressure, hyperglycemia, dyslipidemia) in children between 2-19 years were to be eligible for inclusion in the review. Risk of bias (ROB) in selected RCTs and quality assessment of non-RCT studies were to be assessed by the Cochrane ROB assessment table and New Castle Ottawa scale.
There were no studies on early probiotic administration for prevention of childhood MS (CMS). Follow up studies of two placebo controlled RCTs (n = 233) reported on the effects of early probiotics on one or more components of MS in children aged 2-19 years. Meta-analysis of those two studies could not be performed due to differences in the patient population, type of outcomes studied and the timing of their assessment. Assessment of childhood metabolic outcomes was not the primary objective of these studies. The first study that assessed the effects of prenatal and postnatal supplementation of Lactobacillus rhamnosus GG on body mass index till 10 years, did not report a significant benefit. In the second study, Lactobacillus paracasei 19 was supplemented to healthy term infants from 4-13 mo. No significant effect on body mass index, body composition or metabolic markers was detected.
Current evidence on early probiotic administration to prevent CMS is inadequate. Gaps in knowledge need to be addressed before large RCTs can be planned.
对早期补充益生菌预防儿童代谢综合征(MS)的研究进行系统评价。
采用Cochrane系统评价策略,于2014年12月检索了PubMed、EMBASE、CENTRAL、CINAHL以及美国儿科学会会议的会议记录和试验注册库。选择对母亲和/或婴儿补充益生菌至少4周的随机对照试验(RCT)和非RCT。其中,报告2至19岁儿童MS或其组成部分(肥胖、血压升高、高血糖、血脂异常)的研究有资格纳入本评价。采用Cochrane偏倚风险(ROB)评估表和纽卡斯尔渥太华量表对所选RCT的偏倚风险和非RCT研究的质量进行评估。
尚无关于早期补充益生菌预防儿童MS(CMS)的研究。两项安慰剂对照RCT(n = 233)的随访研究报告了早期益生菌对2至19岁儿童MS一个或多个组成部分的影响。由于患者人群、研究结局类型及其评估时间的差异,无法对这两项研究进行荟萃分析。评估儿童代谢结局并非这些研究的主要目的。第一项评估产前和产后补充鼠李糖乳杆菌GG对10岁前体重指数影响的研究未报告显著益处。在第二项研究中,对4至13个月的健康足月儿补充副干酪乳杆菌19。未检测到对体重指数、身体成分或代谢标志物有显著影响。
目前关于早期补充益生菌预防CMS的证据不足。在规划大型RCT之前,需要填补知识空白。