World Allergy Organization (WAO) Diagnosis and Rationale for Action against Cow's Milk Allergy (DRACMA) guideline update - XI - Milk supplement/replacement formulas for infants and toddlers with CMA - Systematic review.

GRADE approach Infant formulas Meta-analysis Milk allergy Systematic review

Journal

The World Allergy Organization journal
ISSN: 1939-4551
Titre abrégé: World Allergy Organ J
Pays: United States
ID NLM: 101481283

Informations de publication

Date de publication:
Sep 2024
Historique:
received: 15 02 2024
revised: 23 07 2024
accepted: 24 07 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 23 9 2024
Statut: epublish

Résumé

Cow's milk allergy (CMA) is the most complex and common food allergy in infants. Elimination of cow's milk from the diet and replacement with a specialized formula for infants with cow's milk allergy who cannot be breastfed is an established approach to minimize the risk of severe allergic reactions while avoiding nutritional deficiencies. Given the availability of multiple options, such as extensively hydrolyzed cow's milk-based formula (eHF-CM), aminoacid formula (AAF), hydrolyzed rice formula (HRF), and soy formula (SF), there is some uncertainty regarding which formula might represent the most suitable choice with respect to health outcomes. The addition of probiotics to a specialized formula has also been proposed as a potential approach to possibly increase the benefit. We systematically reviewed specialized formulas for infants with CMA to inform the updated World Allergy Organization (WAO) DRACMA guidelines. To systematically review and synthesize the available evidence about the use of specialized formulas for the management of individuals with CMA. We searched from inception PubMed, Medline, Embase, the Cochrane Central Register of Controlled Trials (CENTRAL), and the websites of selected allergy organizations, for randomized and non-randomized trials of any language investigating specialized formulas with or without probiotics. We included all studies irrespective of the language of the original publication. The last search was conducted in January 2024. We synthesized the identified evidence quantitatively or narratively as appropriate and summarized it in the evidence profiles. We conducted this review following the PRISMA, Cochrane methods, and the GRADE approach. We identified 3558 records including 14 randomized trials and 7 observational studies. Very low certainty evidence suggested that in infants with IgE-mediated CMA, eHF-CM, compared with AAF, might have higher probability of outgrowing CMA (risk ratio (RR) 2.32; risk difference (RD) 25 more per 100), while showing potentially lower probability of severe vomiting (RR 0.12, 95% CI 0.02 to 0.88; RD 23 fewer per 100, 95% CI 3 to 26) and developing food protein-induced enterocolitis syndrome (FPIES) (RR 0.15, 95% CI 0.03 to 0.82; RD 34 fewer per 100, 95% CI 7 to 39). We also found, however, that eHF-CM might be inferior to AAF in supporting a physiological growth, with respect to both weight (-5.5% from baseline, 95%CI -9.5% to -1.5%) and length (-0.7 z-score change, 95%CI -1.15 to -0.25) (very low certainty). We found similar effects for eHF-CM, compared with AAF, also in non-IgE CMA. When compared with SF, eHF-CM might favor weight gain for IgE CMA infants (0.23 z-score change, 95%CI 0.01 to 0.45), and tolerance acquisition (RR 1.86, 95%CI 1.03 to 3.37; RD 27%, 95%CI 1%-74%) for non-IgE CMA (both at very low certainty of the evidence (CoE)). The comparison of eHF-CM vs. HRF, and HRF vs. SF, showed no difference in effect (very low certainty). For IgE CMA patients, low certainty evidence suggested that adding probiotics ( Currently available studies comparing eHF-CM, AAF, HRF, and SF provide very low certainty evidence about their effects in infants with IgE-mediated and non-IgE-mediated CMA. Our review revealed several limitations in the current body of evidence, primarily arising from concerns related to the quality of studies, the limited size of the participant populations and most importantly the lack of diversity and standardization in the compared interventions. It is therefore imperative for future studies to be methodologically rigorous and investigate a broader spectrum of available interventions. We encourage clinicians and researchers to review current World Allergy Organization (WAO) Diagnosis and Rationale for Action against Cow's Milk Allergy (DRACMA) Guidelines for suggestions on how to use milk replacement formulas in clinical practice and what additional research would be the most beneficial.

Sections du résumé

Background UNASSIGNED
Cow's milk allergy (CMA) is the most complex and common food allergy in infants. Elimination of cow's milk from the diet and replacement with a specialized formula for infants with cow's milk allergy who cannot be breastfed is an established approach to minimize the risk of severe allergic reactions while avoiding nutritional deficiencies. Given the availability of multiple options, such as extensively hydrolyzed cow's milk-based formula (eHF-CM), aminoacid formula (AAF), hydrolyzed rice formula (HRF), and soy formula (SF), there is some uncertainty regarding which formula might represent the most suitable choice with respect to health outcomes. The addition of probiotics to a specialized formula has also been proposed as a potential approach to possibly increase the benefit. We systematically reviewed specialized formulas for infants with CMA to inform the updated World Allergy Organization (WAO) DRACMA guidelines.
Objective UNASSIGNED
To systematically review and synthesize the available evidence about the use of specialized formulas for the management of individuals with CMA.
Methods UNASSIGNED
We searched from inception PubMed, Medline, Embase, the Cochrane Central Register of Controlled Trials (CENTRAL), and the websites of selected allergy organizations, for randomized and non-randomized trials of any language investigating specialized formulas with or without probiotics. We included all studies irrespective of the language of the original publication. The last search was conducted in January 2024. We synthesized the identified evidence quantitatively or narratively as appropriate and summarized it in the evidence profiles. We conducted this review following the PRISMA, Cochrane methods, and the GRADE approach.
Results UNASSIGNED
We identified 3558 records including 14 randomized trials and 7 observational studies. Very low certainty evidence suggested that in infants with IgE-mediated CMA, eHF-CM, compared with AAF, might have higher probability of outgrowing CMA (risk ratio (RR) 2.32; risk difference (RD) 25 more per 100), while showing potentially lower probability of severe vomiting (RR 0.12, 95% CI 0.02 to 0.88; RD 23 fewer per 100, 95% CI 3 to 26) and developing food protein-induced enterocolitis syndrome (FPIES) (RR 0.15, 95% CI 0.03 to 0.82; RD 34 fewer per 100, 95% CI 7 to 39). We also found, however, that eHF-CM might be inferior to AAF in supporting a physiological growth, with respect to both weight (-5.5% from baseline, 95%CI -9.5% to -1.5%) and length (-0.7 z-score change, 95%CI -1.15 to -0.25) (very low certainty). We found similar effects for eHF-CM, compared with AAF, also in non-IgE CMA. When compared with SF, eHF-CM might favor weight gain for IgE CMA infants (0.23 z-score change, 95%CI 0.01 to 0.45), and tolerance acquisition (RR 1.86, 95%CI 1.03 to 3.37; RD 27%, 95%CI 1%-74%) for non-IgE CMA (both at very low certainty of the evidence (CoE)). The comparison of eHF-CM vs. HRF, and HRF vs. SF, showed no difference in effect (very low certainty). For IgE CMA patients, low certainty evidence suggested that adding probiotics (
Conclusions UNASSIGNED
Currently available studies comparing eHF-CM, AAF, HRF, and SF provide very low certainty evidence about their effects in infants with IgE-mediated and non-IgE-mediated CMA. Our review revealed several limitations in the current body of evidence, primarily arising from concerns related to the quality of studies, the limited size of the participant populations and most importantly the lack of diversity and standardization in the compared interventions. It is therefore imperative for future studies to be methodologically rigorous and investigate a broader spectrum of available interventions. We encourage clinicians and researchers to review current World Allergy Organization (WAO) Diagnosis and Rationale for Action against Cow's Milk Allergy (DRACMA) Guidelines for suggestions on how to use milk replacement formulas in clinical practice and what additional research would be the most beneficial.

Identifiants

pubmed: 39310372
doi: 10.1016/j.waojou.2024.100947
pii: S1939-4551(24)00078-4
pmc: PMC11415968
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100947

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

HJS and JLB, on behalf of McMaster University, received a research grant from the World Allergy Organization to conduct this review that was deposited into the university research account. RS participated as a clinical investigator, and/or advisory board member, and/or consultant, and/or speaker for Abbott, Else, and Nestlé. HS serves as a board member of the International Scientific Association for Probiotics and Prebiotics (ISAPP), an unpaid and voluntary role. They have participated as a clinical investigator, advisory board member, consultant, and speaker for several companies, including Arla, BioGaia, Biocodex, Danone, Dicofarm, Nestlé, NNI, Nutricia, Mead Johnson, and Novalac. YV has participated as a clinical investigator, and/or advisory board member, and/or consultant, and/or speaker for Abbott Nutrition, Alba Health, Arla, Ausnutria, Biogaia, By Heart, CHR Hansen, Danone, ELSE Nutrition, Friesland Campina, Nestle Health Science, Nestle Nutrition Institute, Nutricia, Mead Johnson Nutrition, Pileje, Sanulac, United Pharmaceuticals (Novalac), Yakult, Wyeth. SW is the president of the Canadian Allergy Asthma and Immunology Foundation, and participated as a clinical investigator, and/or advisory board member, and/or consultant, and/or speaker for Pfizer, Kaleo, Bausch Health, GSK, AZ, Sanofi, CSL Behring, Leo, AbbVie, Takeda, Medexus Pharma, MiravoHealth, BioCryst, ALK, Novartis. They also covered the positions of: BOD Asthma Canada, CHAEN. MS works for Allergy & Anaphylaxis Australis, which receives unrestricted educational grants from infant formula companies. AW works for Allergy UK works with corporate partners including those providing foods for special medical purposes, such as Nutricia/Danone, Abbott, Reckitt Benckiser/Mead Johnson. They have been a speakers for 2 Nutricia symposia, with honoraria being paid to the charity. All other authors declare that they have no relevant conflicts of interest to disclose.

Auteurs

Antonio Bognanni (A)

Department of Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Ontario, Canada.
Clinical Epidemiology and Research Center (CERC), Humanitas University & Humanitas Research Hospital, Pieve Emanuele, Milano, Italy.
Department of Medicine, Evidence in Allergy Group, McMaster University, Hamilton, Ontario, Canada.

Ramon T Firmino (RT)

Academic Unit of Biological Sciences, Federal University of Campina Grande, Patos, Paraíba, Brazil.

Stefania Arasi (S)

Translational Research in Pediatric Specialties Area, Division of Allergy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Derek K Chu (DK)

Department of Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Ontario, Canada.
Department of Medicine, Evidence in Allergy Group, McMaster University, Hamilton, Ontario, Canada.
Department of Medicine, Division of Clinical Immunology and Allergy, McMaster University, Hamilton, Ontario, Canada.

Alexandro W L Chu (AWL)

Department of Medicine, Evidence in Allergy Group, McMaster University, Hamilton, Ontario, Canada.
Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Siw Waffenschmidt (S)

Institute for Quality and Efficiency in Health Care, Cologne, Germany.

Arnav Agarwal (A)

Department of Medicine, Division of Internal Medicine, McMaster University, Hamilton, Ontario, Canada.

Piotr Dziechciarz (P)

Medical University of Warsaw, Warsaw, Poland.

Andrea Horvath (A)

Medical University of Warsaw, Warsaw, Poland.

Hanako Mihara (H)

Clinical Development Infectious Disease, Moderna Japan Co., Ltd., Japan.

Yetiani Roldan (Y)

McMaster University, Hamilton, Ontario, Canada.

Luigi Terracciano (L)

Pediatric Primary Care, National Pediatric Health Care System, Milan, Italy.
Italian Society of Preventive and Social Pediatrics (SIPPS), Italy.

Alberto Martelli (A)

Italian Society of Allergy and Pediatric Immunology (SIAIP), Italy.

Anna Starok (A)

Evidence Prime Inc., Krakow, Poland.

Maria Said (M)

Allergy & Anaphylaxis Australia, Sydney, Australia.

Raanan Shamir (R)

Institute for Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center of Israel, Faculty of Medical and Health Sciences, Tel Aviv University, Israel.

Ignacio J Ansotegui (IJ)

Department of Allergy & Immunology, Hospital Quironsalud Bizkaia, Erandio, Bilbao, Spain.

Lamia Dahdah (L)

Translational Research in Pediatric Specialties Area, Division of Allergy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Motohiro Ebisawa (M)

Clinical Research Center for Allergy and Rheumatology, NHO Sagamihara National Hospital, Kanagawa, Japan.

Elena Galli (E)

Pediatric Allergy Unit, Research Center, San Pietro Hospital - Fatebenefratelli, Rome, Italy.

Rose Kamenwa (R)

Department of Pediatrics and Child Health, Aga Khan University Hospital, Nairobi, Kenya.

Gideon Lack (G)

Department of Women and Children's Health/Peter Gorer Department of Immunobiology, School of Life Course Sciences, Faculty of Life Sciences & Medicine, King's College London, United Kingdom.
Evelina London Children's Hospital, Guy's and St Thomas' Hospital NHS Foundation Trust, United Kingdom.

Haiqi Li (H)

Department of Primary Child Care, Children's Hospital, Chongqing Medical University, China.

Ruby Pawankar (R)

Department of Pediatrics. Nippon Medical School, Tokyo, Japan.

Amena Warner (A)

Allergy UK, Crayford, Kingdom, United Kingdom.

Gary Wing Kin Wong (GWK)

Department of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong.

Martin Bozzola (M)

Pediatric Allergy and Immunology Section, Dept of Pediatrics, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.

Amal Assa'Ad (A)

Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, and the University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Christophe Dupont (C)

Clinique Marcel Sembat, Ramsay Group, Boulogne-Billancourt, France.

Sami Bahna (S)

Louisiana State University Health Sciences Center - Shreveport, Shreveport, LA, USA.

Jonathan Spergel (J)

Division of Allergy and Immunology, Children's Hospital of Philadelphia, USA.
Perelman School of Medicine at University of Pennsylvania, Philadelphia, PA, USA.

Carina Venter (C)

Section of Allergy and Clinical Immunology, University of Colorado, USA.
Children's Hospital Colorado. Denver, Colorado, USA.

Hania Szajewska (H)

Department of Paediatrics, The Medical University of Warsaw, Warsaw, Poland.

Anna H Nowak-Wegrzyn (AH)

Department of Pediatrics, Hassenfeld Children's Hospital, New York University, Grossman School of Medicine, New York, NY, USA.
Department of Pediatrics, Gastroenterology and Nutrition, Collegium Medicum, University of Warmia and Mazury, Olsztyn, Poland.

Yvan Vandenplas (Y)

Vrije Universiteit Brussel (VUB), UZ Brussel, Belgium.
KidZ Health Castle, Brussels, Belgium.

Nikolaos G Papadopoulos (NG)

Allergy Department, 2nd Pediatric Clinic, University of Athens, Athens, Greece.
Lydia Becker Institute, University of Manchester, Manchester, United Kingdom.

Susan Waserman (S)

Department of Medicine, Division of Clinical Immunology and Allergy, McMaster University, Hamilton, Ontario, Canada.

Alessandro Fiocchi (A)

Translational Research in Pediatric Specialties Area, Division of Allergy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Holger J Schünemann (HJ)

Clinical Epidemiology and Research Center (CERC), Humanitas University & Humanitas Research Hospital, Pieve Emanuele, Milano, Italy.

Jan L Brożek (JL)

Department of Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Ontario, Canada.
Department of Medicine, Division of Clinical Immunology and Allergy, McMaster University, Hamilton, Ontario, Canada.

Classifications MeSH