Efficacy of lactoferrin supplementation in pediatric infections: a systematic review and meta-analysis

被引:0
作者
Mayorga, Valerie S. [1 ]
Navarro, Rafaella [1 ]
Roldan, Victor D. Torres [2 ]
Urtecho, Meritxell [3 ]
Tipe, Silvia [4 ]
Calvert, Bea [5 ]
Wright, Laura A. [5 ]
Ochoa, Theresa J. [1 ,4 ]
机构
[1] Univ Peruana Cayetano Heredia, Inst Med Trop Alexander von Humboldt, Lima, Peru
[2] Tulane Univ, Tulane Sch Med, Dept Pediat, New Orleans, LA USA
[3] Tulane Univ, Tulane Sch Med, Dept Internal Med, New Orleans, LA USA
[4] Univ Peruana Cayetano Heredia, Fac Med, Lima, Peru
[5] Tulane Univ, New Orleans, LA USA
关键词
lactoferrin; children; adolescent; diarrhea; respiratory infections; sepsis; RESPIRATORY-TRACT INFECTIONS; RANDOMIZED CONTROLLED-TRIAL; LATE-ONSET SEPSIS; BOVINE LACTOFERRIN; DOUBLE-BLIND; PREVENTION; DIARRHEA; INFANTS; TALACTOFERRIN; IRON;
D O I
10.1139/bcb-2024-0181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pediatric infections account for approximately one-third of all deaths in children under 5 years globally. Lactoferrin (LF) supplementation has the potential to reduce infection-related morbidity due to its antimicrobial, anti-inflammatory, and immunoregulatory properties. We conducted a systematic review and meta-analysis of oral LF supplementation randomized controlled trials in population under 18 years old. The primary outcomes were infection-associated outcomes: late onset sepsis (LOS), diarrhea, and upper respiratory infections (URIs). We also analyzed mortality among LOS studies. Of 1594 citations identified, 25 studies met eligibility criteria, including 10 studies of LOS, 14 of diarrhea, and 8 of URI. LF supplementation was associated with fewer patients with culture-proven or probable neonatal LOS compared to placebo (odds ratio (OR): 0.60; 95% confidence interval (CI): 0.42-0.86), with fewer patients with diarrhea compared to placebo in children (OR: 0.56; 95% CI: 0.41-0.75), and no significant fewer patients with URI (OR: 0.61; 95% CI: 0.27-1.40). Before LF can be used as a public health intervention, it is necessary to refine some aspects of the design of future trials. Ideally these trials should be conducted in countries with the highest burden of infections, where the potential benefit is expected to have the largest impact.
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