RETRACTED: Infant formulas containing hydrolysed protein for prevention of allergic disease and food allergy (Retracted Article)

被引:0
|
作者
Osborn, David A. [1 ]
Sinn, John K. H. [2 ]
Jones, Lisa J. [1 ]
机构
[1] Univ Sydney, Discipline Obstet Gynaecol & Neonatol, Cent Clin Sch, Sydney, NSW, Australia
[2] Univ Sydney, Royal North Shore Hosp, Dept Neonatol, Sydney, NSW 2065, Australia
基金
美国国家卫生研究院;
关键词
Dietary Proteins; Food Hypersensitivity [prevention & control; Hydrolysis; Infant Formula [chemistry; Milk Hypersensitivity [prevention & control; Milk; Human; Protein Hydrolysates [administration & dosage; Randomized Controlled Trials as Topic; Synapsins; HIGH-RISK INFANTS; HEALTHY TERM INFANTS; COWS MILK-PROTEINS; DIETARY INTERVENTION PROGRAM; AMINO-ACID-CONCENTRATIONS; PARTIAL WHEY HYDROLYSATE; BRIEF NEONATAL EXPOSURE; ZUFF-STUDY-PROGRAM; DOUBLE-BLIND; ATOPIC-DERMATITIS;
D O I
10.1002/14651858.CD003664.pub4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Allergy is common and may be associated with foods, including cow's milk formula (CMF). Formulas containing hydrolysed proteins have been used to treat infants with allergy. However, it is unclear whether hydrolysed formulas can be advocated for prevention of allergy in infants. Objectives To compare effects on allergy and food allergy when infants are fed a hydrolysed formula versus CMF or human breast milk. If hydrolysed formulas are effective, to determine what type of hydrolysed formula is most effective, including extensively or partially hydrolysed formula (EHF/PHF). To determine which infants at low or high risk of allergy and which infants receiving early, shortterm or prolonged formula feeding may benefit from hydrolysed formulas. Search methods We used the standard search strategy of the Cochrane Neonatal Review Group supplemented by cross referencing of previous reviews and publications (updated August 2016). Selection criteria We searched for randomised and quasi-randomised trials that compared use of a hydrolysed formula versus human milk or CMF. Trials with >= 80% follow-up of participants were eligible for inclusion. Data collection and analysis We independently assessed eligibility of studies for inclusion, methodological quality and data extraction. Primary outcomes included clinical allergy, specific allergy and food allergy. We conducted meta-analysis using a fixed-effect (FE) model. Main results Two studies assessed the effect of three to four days' infant supplementation with an EHF whilst in hospital after birth versus pasteurised human milk feed. Results showed no difference in infant allergy or childhood cow's milk allergy (CMA). No eligible trials compared prolonged hydrolysed formula versus human milk feeding. Two studies assessed the effect of three to four days' infant supplementation with an EHF versus a CMF. One large quasi-random study reported a reduction in infant CMA of borderline significance among low-risk infants (risk ratio (RR) 0.62, 95% confidence interval (CI) 0.38 to 1.00). Prolonged infant feeding with a hydrolysed formula compared with a CMF was associated with a reduction in infant allergy (eight studies, 2852 infants; FE RR 0.82, 95% CI 0.72 to 0.95; risk difference (RD) -0.04, 95% CI -0.08 to -0.01; number needed to treat for an additional beneficial outcome (NNTB) 25, 95% CI 12.5 to 100) and infant CMA (two studies, 405 infants; FE RR 0.38, 95% CI 0.16 to 0.86). We had substantial methodological concerns regarding studies and concerns regarding publication bias, as substantial numbers of studies including those in high-risk infants have not comprehensively reported allergy outcomes (GRADE quality of evidence ' very low'). Prolonged infant feeding with a hydrolysed formula compared with a CMF was not associated with a difference in childhood allergy and led to no differences in specific allergy, including infant and childhood asthma, eczema and rhinitis and infant food allergy. Many of the analyses assessing specific allergy are underpowered. Subroup analyses showed that infant allergy was reduced in studies that enrolled infants at high risk of allergy who used a hydrolysed formula compared with a CMF; used a PHF compared with a CMF; used prolonged and exclusive feeding of a hydrolysed formula compared with a CMF; and used a partially hydrolysed whey formula compared with a CMF. Studies that enrolled infants at high risk of allergy; used a PHF compared with a CMF; used prolonged and exclusive feeding of a hydrolysed formula compared with a CMF; and used a partially hydrolysed whey formula compared with a CMF found a reduction in infant CMA. Authors' conclusions We found no evidence to support short-term or prolonged feeding with a hydrolysed formula compared with exclusive breast feeding for prevention of allergy. Very low-quality evidence indicates that short-term use of an EHF compared with a CMF may prevent infant CMA. In infants at high risk of allergy not exclusively breast fed, very low-quality evidence suggests that prolonged hydrolysed formula feeding compared with CMF feeding reduces infant allergy and infant CMA. Studies have found no difference in childhood allergy and no difference in specific allergy, including infant and childhood asthma, eczema and rhinitis and infant food allergy. Very low-quality evidence shows that prolonged use of a partially hydrolysed formula compared with a CMF for partial or exclusive feeding was associated with a reduction in infant allergy incidence and CMA incidence, and that prolonged use of an EHF versus a PHF reduces infant food allergy.
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