Effect of an Exclusive Human Milk Diet on the Gut Microbiome in Preterm Infants A Randomized Clinical Trial

被引:20
作者
Embleton, Nicholas D. [1 ,2 ]
Sproat, Thomas [1 ,3 ]
Uthaya, Sabita [4 ,5 ]
Young, Gregory R. [6 ]
Garg, Shalabh [7 ]
Vasu, Vimal [8 ]
Masi, Andrea C. [3 ]
Beck, Lauren [3 ]
Modi, Neena [4 ,5 ]
Stewart, Christopher J. [3 ]
Berrington, Janet E. [1 ,3 ]
机构
[1] Newcastle Hosp NHS Trust, Royal Victoria Infirm, Newcastle Upon Tyne, England
[2] Newcastle Univ, Populat Hlth Sci Inst, Newcastle Upon Tyne, England
[3] Newcastle Univ, Translat & Clin Res Inst, Newcastle Upon Tyne, England
[4] Imperial Coll London, Sch Publ Hlth, Sect Neonatal Med, London, England
[5] NHS Fdn Trust, Chelsea & Westminster Hosp, London, England
[6] Northumbria Univ, Newcastle Upon Tyne, England
[7] James Cook Univ Hosp, Middlesbrough, England
[8] William Harvey Hosp, Ashford, Kent, England
关键词
BIRTH-WEIGHT INFANTS; NECROTIZING ENTEROCOLITIS; DONOR MILK; NUTRITION; FORMULA; HEALTH; ONSET;
D O I
10.1001/jamanetworkopen.2023.1165
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE The effect of using an exclusive human milk diet compared with one that uses bovine products in preterm infants is uncertain, but some studies demonstrate lower rates of key neonatal morbidities. A potential mediating pathway is the gut microbiome. OBJECTIVE To determine the effect of an exclusive human milk diet on gut bacterial richness, diversity, and proportions of specific taxa in preterm infants from enrollment to 34 weeks' postmenstrual age. DESIGN, SETTING, AND PARTICIPANTS In this randomized clinical trial conducted at 4 neonatal intensive care units in the United Kingdom from 2017 to 2020, microbiome analyses were blind to group. Infants less than 30 weeks' gestation who had only received own mother's milk were recruited before 72 hours of age. Statistical analysis was performed from July 2019 to September 2021. INTERVENTIONS Exclusive human milk diet using pasteurized human milk for any shortfall in mother's own milk supply and human milk-derived fortifiers (intervention) compared with bovine formula and bovine-derived fortifier (control) until 34 weeks' postmenstrual age. Fortifier commenced less than 48 hours of tolerating 150 mL/kg per day. MAIN OUTCOMES AND MEASURES Gut microbiome profile including alpha and beta diversity, and presence of specific bacterial taxa. RESULTS Of 126 preterm infants enrolled in the study, 63 were randomized to control (median [IQR] gestation: 27.0 weeks [26.0-28.1 weeks]; median [IQR] birthweight: 910 g [ 704-1054 g]; 32 [51%] male) and 63were randomized to intervention (median [IQR] gestation: 27.1 weeks [25.7-28.1weeks]; median [IQR] birthweight: 930 g [733-1095 g]; 38 [60%] male); 472 stool samples from 116 infants were analyzed. There were no differences in bacterial richness or Shannon diversity over time, or at 34weeks between trial groups. The exclusive human milk diet group had reduced relative abundance of Lactobacillus after adjustment for confounders (coefficient estimate, 0.056; P =.03), but not after false discovery rate adjustment. There were no differences in time to full feeds, necrotizing enterocolitis, or other key neonatal morbidities. CONCLUSIONS AND RELEVANCE In this randomized clinical trial in preterm infants using human milk-derived formula and/or fortifier to enable an exclusive human milk diet, there were no effects on overall measures of gut bacterial diversity but therewere effects on specific bacterial taxa previously associated with human milk receipt. These findings suggest that the clinical impact of human milk-derived products is not modulated via microbiomic mechanisms.
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页数:11
相关论文
共 37 条
[31]   An Exclusively Human Milk-Based Diet Is Associated with a Lower Rate of Necrotizing Enterocolitis than a Diet of Human Milk and Bovine Milk-Based Products [J].
Sullivan, Sandra ;
Schanler, Richard J. ;
Kim, Jae H. ;
Patel, Aloka L. ;
Trawoger, Rudolf ;
Kiechl-Kohlendorfer, Ursula ;
Chan, Gary M. ;
Blanco, Cynthia L. ;
Abrams, Steven ;
Cotten, C. Michael ;
Laroia, Nirupama ;
Ehrenkranz, Richard A. ;
Dudell, Golde ;
Cristofalo, Elizabeth A. ;
Meier, Paula ;
Lee, Martin L. ;
Rechtman, David J. ;
Lucas, Alan .
JOURNAL OF PEDIATRICS, 2010, 156 (04) :562-U83
[32]   DoMINO: Donor milk for improved neurodevelopmental outcomes [J].
Unger, Sharon ;
Gibbins, Sharyn ;
Zupancic, John ;
O'Connor, Deborah L. .
BMC PEDIATRICS, 2014, 14
[33]   Donor Human Milk Protects against Bronchopulmonary Dysplasia: A Systematic Review and Meta-Analysis [J].
Villamor-Martinez, Eduardo ;
Pierro, Maria ;
Cavallaro, Giacomo ;
Mosca, Fabio ;
Kramer, Boris W. ;
Villamor, Eduardo .
NUTRIENTS, 2018, 10 (02)
[34]  
Wickham H2016ggplot2, elegant graphics for data analysis
[35]   The metabolomics of necrotising enterocolitis in preterm babies: an exploratory study [J].
Wilcock, Amy ;
Begley, Paul ;
Stevens, Adam ;
Whatmore, Andrew ;
Victor, Suresh .
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2016, 29 (05) :758-762
[36]   Human Milk Feeding as a Protective Factor for Retinopathy of Prematurity: A Meta-analysis [J].
Zhou, Jianguo ;
Shukla, Vivek V. ;
John, Denny ;
Chen, Chao .
PEDIATRICS, 2015, 136 (06) :E1576-E1586
[37]   Use of donor breast milk in neonatal units in the UK [J].
Zipitis, Christos S. ;
Ward, Jonathan ;
Bajaj, Rohini .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2015, 100 (03) :F279-F280