Li Pin, Uma Mageswary Mageswaran, Taib Fahisham, Koo Thai Hau, Yusof Azianey, Hamid Intan Juliana Abd, Jiang Hua, Liong Min-Tze, Ali Adli, Zhang Yumei
Department of Nutrition and Food Hygiene, School of Public Health, Peking University Health Science Center, Beijing 100191, China.
School of Industrial Technology, Universiti Sains Malaysia, Gelugor 11800, Malaysia.
Nutrients. 2025 Jun 26;17(13):2127. doi: 10.3390/nu17132127.
The aim of this study was to examine the safety and tolerance of YLGB-1496 ( YLGB-1496) in toddlers with respiratory illness. : In this randomized controlled trial, 120 toddlers with respiratory illness were randomly assigned to the probiotic (YLGB-1496) or control group for a 12-week intervention. Follow-up examinations were conducted at baseline (week 0) and at weeks 6 and 12 of the intervention. Toddlers' height and weight were measured by trained personnel, and defecation characteristics and gastrointestinal symptoms were recorded by parents or guardians. Stool samples were collected to determine the fecal pH, fecal calprotectin (FC) concentration, and fecal α1-antitrypsin (AAT) concentration. : A total of 115 toddlers completed the 12-week intervention (58 in the YLGB-1496 group and 57 in the control group). The height-for-age Z score (HAZ) in the YLGB-1496 group was significantly greater than that in the control group ( = 0.006). The weight-for-age Z score (WAZ) in the YLGB-1496 group increased between weeks 6 and 12, whereas the WAZ in the control group continuously decreased during the intervention. No differences in the frequency or consistency of defecation between the groups were observed. Toddlers in the YLGB-1496 group had lower incidences of poor appetite, nausea, vomiting, stomachache, lower abdominal pain, diarrhea, and dehydration ( < 0.05) but higher fecal AAT concentrations ( = 0.008) than did those in the control group. No differences in the fecal pH or FC concentration were observed between the groups. : YLGB-1496 demonstrated excellent safety and tolerability in toddlers and effectively reduced the gastrointestinal discomfort associated with respiratory illnesses.
本研究旨在探讨YLGB - 1496对患有呼吸道疾病的幼儿的安全性和耐受性。在这项随机对照试验中,120名患有呼吸道疾病的幼儿被随机分配到益生菌(YLGB - 1496)组或对照组,进行为期12周的干预。在基线(第0周)以及干预的第6周和第12周进行随访检查。由经过培训的人员测量幼儿的身高和体重,父母或监护人记录排便特征和胃肠道症状。收集粪便样本以测定粪便pH值、粪便钙卫蛋白(FC)浓度和粪便α1 -抗胰蛋白酶(AAT)浓度。共有115名幼儿完成了12周的干预(YLGB - 1496组58名,对照组57名)。YLGB - 1496组的年龄别身高Z评分(HAZ)显著高于对照组(P = 0.006)。YLGB - 1496组的年龄别体重Z评分(WAZ)在第6周和第12周之间有所增加,而对照组的WAZ在干预期间持续下降。两组之间在排便频率或稠度方面未观察到差异。YLGB - 1496组幼儿食欲不振、恶心、呕吐、胃痛、下腹痛、腹泻和脱水的发生率较低(P < 0.05),但粪便AAT浓度高于对照组(P = 0.008)。两组之间在粪便pH值或FC浓度方面未观察到差异。YLGB - 1496在幼儿中表现出极佳的安全性和耐受性,并有效减轻了与呼吸道疾病相关的胃肠道不适。