An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy
Human milk, due to its unique composition, is the optimal standard for infant nutrition. Osteopontin (OPN) is abundant in human milk but not bovine milk. The addition of bovine milk osteopontin (bmOPN) to formula may replicate OPN’s concentration and function in human milk. To address safety concern...
| 发表在: | Frontiers in Nutrition |
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| Main Authors: | , , , , , , , , , , , |
| 格式: | 文件 |
| 语言: | 英语 |
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Frontiers Media S.A.
2024-06-01
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| 在线阅读: | https://www.frontiersin.org/articles/10.3389/fnut.2024.1404303/full |
| _version_ | 1850339057256628224 |
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| author | Stephen A. Fleming Sarah M. Reyes Sharon M. Donovan Olle Hernell Rulan Jiang Bo Lönnerdal Josef Neu Lawrence Steinman Esben S. Sørensen Christina E. West Ronald Kleinman Ronald Kleinman John C. Wallingford |
| author_facet | Stephen A. Fleming Sarah M. Reyes Sharon M. Donovan Olle Hernell Rulan Jiang Bo Lönnerdal Josef Neu Lawrence Steinman Esben S. Sørensen Christina E. West Ronald Kleinman Ronald Kleinman John C. Wallingford |
| author_sort | Stephen A. Fleming |
| collection | DOAJ |
| container_title | Frontiers in Nutrition |
| description | Human milk, due to its unique composition, is the optimal standard for infant nutrition. Osteopontin (OPN) is abundant in human milk but not bovine milk. The addition of bovine milk osteopontin (bmOPN) to formula may replicate OPN’s concentration and function in human milk. To address safety concerns, we convened an expert panel to assess the adequacy of safety data and physiological roles of dietary bmOPN in infancy. The exposure of breastfed infants to human milk OPN (hmOPN) has been well-characterized and decreases markedly over the first 6 months of lactation. Dietary bmOPN is resistant to gastric and intestinal digestion, absorbed and cleared from circulation within 8–24 h, and represents a small portion (<5%) of total plasma OPN. Label studies on hmOPN suggest that after 3 h, intact or digested OPN is absorbed into carcass (62%), small intestine (23%), stomach (5%), and small intestinal perfusate (4%), with <2% each found in the cecum, liver, brain, heart, and spleen. Although the results are heterogenous with respect to bmOPN’s physiologic impact, no adverse impacts have been reported across growth, gastrointestinal, immune, or brain-related outcomes. Recombinant bovine and human forms demonstrate similar absorption in plasma as bmOPN, as well as effects on cognition and immunity. The panel recommended prioritization of trials measuring a comprehensive set of clinically relevant outcomes on immunity and cognition to confirm the safety of bmOPN over that of further research on its absorption, distribution, metabolism, and excretion. This review offers expert consensus on the adequacy of data available to assess the safety of bmOPN for use in infant formula, aiding evidence-based decisions on the formulation of infant formula. |
| format | Article |
| id | doaj-art-eed2ae986a36498689796d737fbbeba8 |
| institution | Directory of Open Access Journals |
| issn | 2296-861X |
| language | English |
| publishDate | 2024-06-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| spelling | doaj-art-eed2ae986a36498689796d737fbbeba82025-08-19T23:14:58ZengFrontiers Media S.A.Frontiers in Nutrition2296-861X2024-06-011110.3389/fnut.2024.14043031404303An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancyStephen A. Fleming0Sarah M. Reyes1Sharon M. Donovan2Olle Hernell3Rulan Jiang4Bo Lönnerdal5Josef Neu6Lawrence Steinman7Esben S. Sørensen8Christina E. West9Ronald Kleinman10Ronald Kleinman11John C. Wallingford12Traverse Science, Inc., Mundelein, IL, United StatesRev Bioscience, LLC, Boise, ID, United StatesDepartment of Food Science and Human Nutrition, University of Illinois Urbana-Champaign, Urbana, IL, United StatesDepartment of Clinical Sciences and Pediatrics, Umeå University, Umeå, SwedenDepartment of Nutrition, University of California, Davis, Davis, CA, United StatesDepartment of Nutrition, University of California, Davis, Davis, CA, United StatesDepartment of Pediatrics, Division of Neonatology, University of Florida, Gainesville, FL, United StatesDepartments of Pediatrics and of Neurology and Neurological Sciences, Interdepartmental Program in Immunology, Beckman Center for Molecular Medicine, Stanford University School of Medicine, Stanford, CA, United StatesDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, DenmarkDepartment of Clinical Sciences and Pediatrics, Umeå University, Umeå, SwedenHarvard Medical School, Boston, MA, United States0Department of Pediatrics, Massachusetts General Hospital, Boston, MA, United States1Nutrispectives, LLC, Spokane, WA, United StatesHuman milk, due to its unique composition, is the optimal standard for infant nutrition. Osteopontin (OPN) is abundant in human milk but not bovine milk. The addition of bovine milk osteopontin (bmOPN) to formula may replicate OPN’s concentration and function in human milk. To address safety concerns, we convened an expert panel to assess the adequacy of safety data and physiological roles of dietary bmOPN in infancy. The exposure of breastfed infants to human milk OPN (hmOPN) has been well-characterized and decreases markedly over the first 6 months of lactation. Dietary bmOPN is resistant to gastric and intestinal digestion, absorbed and cleared from circulation within 8–24 h, and represents a small portion (<5%) of total plasma OPN. Label studies on hmOPN suggest that after 3 h, intact or digested OPN is absorbed into carcass (62%), small intestine (23%), stomach (5%), and small intestinal perfusate (4%), with <2% each found in the cecum, liver, brain, heart, and spleen. Although the results are heterogenous with respect to bmOPN’s physiologic impact, no adverse impacts have been reported across growth, gastrointestinal, immune, or brain-related outcomes. Recombinant bovine and human forms demonstrate similar absorption in plasma as bmOPN, as well as effects on cognition and immunity. The panel recommended prioritization of trials measuring a comprehensive set of clinically relevant outcomes on immunity and cognition to confirm the safety of bmOPN over that of further research on its absorption, distribution, metabolism, and excretion. This review offers expert consensus on the adequacy of data available to assess the safety of bmOPN for use in infant formula, aiding evidence-based decisions on the formulation of infant formula.https://www.frontiersin.org/articles/10.3389/fnut.2024.1404303/fullinfantmilkosteopontinsafetyimmunityneurodevelopment |
| spellingShingle | Stephen A. Fleming Sarah M. Reyes Sharon M. Donovan Olle Hernell Rulan Jiang Bo Lönnerdal Josef Neu Lawrence Steinman Esben S. Sørensen Christina E. West Ronald Kleinman Ronald Kleinman John C. Wallingford An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy infant milk osteopontin safety immunity neurodevelopment |
| title | An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy |
| title_full | An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy |
| title_fullStr | An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy |
| title_full_unstemmed | An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy |
| title_short | An expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy |
| title_sort | expert panel on the adequacy of safety data and physiological roles of dietary bovine osteopontin in infancy |
| topic | infant milk osteopontin safety immunity neurodevelopment |
| url | https://www.frontiersin.org/articles/10.3389/fnut.2024.1404303/full |
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