Milk A1 and A2 Peptides and Diabetes
Food-derived peptides, specifically those derived from milk, may adversely affect health by increasing the risk of insulin-dependent diabetes. This position is based on the relationship of type 1 diabetes (T1D) and the consumption of variants A1 and B β-casein from cow’s milk. It appears that β-caso...
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description | Food-derived peptides, specifically those derived from milk, may adversely affect health by increasing the risk of insulin-dependent diabetes. This position is based on the relationship of type 1 diabetes (T1D) and the consumption of variants A1 and B β-casein from cow’s milk. It appears that β-casomorphin-7 (BCM-7) from β-casein may function as an immunosuppressant and impair tolerance to dietary antigens in the gut immune system, which, in turn, may contribute to the onset of T1D. There are thirteen genetic variants of β-casein in dairy cattle. Among those variants are A1, A2, and B, which are also found in human milk. The amino acid sequences of β-casomorphins among these bovine variants and those found in human milk are similar, often differing only by a single amino acid. In vitro studies indicate BCM-7 can be produced from A1 and B during typical digestive processes; however, BCM-7 is not a product of A2 digestion. Evidence from several epidemiological studies and animal models does not support the association of milk proteins, even proteins in breast milk, and the development of T1D. Ecological data, primarily based on A1/ A2 variations among livestock breeds, do not demonstrate causation, even among countries where there is considerable dairy consumption. |
doi_str_mv | 10.1159/000325584 |
format | Conference Proceeding |
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This position is based on the relationship of type 1 diabetes (T1D) and the consumption of variants A1 and B β-casein from cow’s milk. It appears that β-casomorphin-7 (BCM-7) from β-casein may function as an immunosuppressant and impair tolerance to dietary antigens in the gut immune system, which, in turn, may contribute to the onset of T1D. There are thirteen genetic variants of β-casein in dairy cattle. Among those variants are A1, A2, and B, which are also found in human milk. The amino acid sequences of β-casomorphins among these bovine variants and those found in human milk are similar, often differing only by a single amino acid. In vitro studies indicate BCM-7 can be produced from A1 and B during typical digestive processes; however, BCM-7 is not a product of A2 digestion. Evidence from several epidemiological studies and animal models does not support the association of milk proteins, even proteins in breast milk, and the development of T1D. Ecological data, primarily based on A1/ A2 variations among livestock breeds, do not demonstrate causation, even among countries where there is considerable dairy consumption.</description><identifier>ISSN: 1664-2147</identifier><identifier>ISBN: 9783805595865</identifier><identifier>ISBN: 3805595867</identifier><identifier>EISSN: 1664-2155</identifier><identifier>EISSN: 1662-3878</identifier><identifier>EISBN: 9783805595872</identifier><identifier>EISBN: 3805595875</identifier><identifier>DOI: 10.1159/000325584</identifier><identifier>PMID: 21335999</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Animals ; Caseins - genetics ; Caseins - immunology ; Cattle ; Chapter ; Diabetes Mellitus, Type 1 - etiology ; Genetic Variation ; Humans ; Milk - adverse effects ; Milk - chemistry ; Milk - immunology ; Peptide Fragments - genetics ; Peptide Fragments - immunology</subject><ispartof>Nestle Nutrition workshop series. Paediatric programme, 2011, Vol.67, p.187-195</ispartof><rights>2011 S. Karger AG, Basel</rights><rights>Copyright © 2011 S. Karger AG, Basel.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c276t-bae9b4f36cffa676b19698b992ab4582b819729e7d64a5dc406fe317d128f7293</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,779,780,784,793,26081,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21335999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Michaelsen KF</contributor><contributor>Hernell O</contributor><contributor>Clemens RA</contributor><creatorcontrib>Clemens, Roger A.</creatorcontrib><title>Milk A1 and A2 Peptides and Diabetes</title><title>Nestle Nutrition workshop series. Paediatric programme</title><addtitle>Nestle Nutr Workshop Ser Pediatr Program</addtitle><description>Food-derived peptides, specifically those derived from milk, may adversely affect health by increasing the risk of insulin-dependent diabetes. This position is based on the relationship of type 1 diabetes (T1D) and the consumption of variants A1 and B β-casein from cow’s milk. It appears that β-casomorphin-7 (BCM-7) from β-casein may function as an immunosuppressant and impair tolerance to dietary antigens in the gut immune system, which, in turn, may contribute to the onset of T1D. There are thirteen genetic variants of β-casein in dairy cattle. Among those variants are A1, A2, and B, which are also found in human milk. The amino acid sequences of β-casomorphins among these bovine variants and those found in human milk are similar, often differing only by a single amino acid. In vitro studies indicate BCM-7 can be produced from A1 and B during typical digestive processes; however, BCM-7 is not a product of A2 digestion. Evidence from several epidemiological studies and animal models does not support the association of milk proteins, even proteins in breast milk, and the development of T1D. Ecological data, primarily based on A1/ A2 variations among livestock breeds, do not demonstrate causation, even among countries where there is considerable dairy consumption.</description><subject>Animals</subject><subject>Caseins - genetics</subject><subject>Caseins - immunology</subject><subject>Cattle</subject><subject>Chapter</subject><subject>Diabetes Mellitus, Type 1 - etiology</subject><subject>Genetic Variation</subject><subject>Humans</subject><subject>Milk - adverse effects</subject><subject>Milk - chemistry</subject><subject>Milk - immunology</subject><subject>Peptide Fragments - genetics</subject><subject>Peptide Fragments - immunology</subject><issn>1664-2147</issn><issn>1664-2155</issn><issn>1662-3878</issn><isbn>9783805595865</isbn><isbn>3805595867</isbn><isbn>9783805595872</isbn><isbn>3805595875</isbn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2011</creationdate><recordtype>conference_proceeding</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLw0AUhccXttQu_AMSQXAVndedmbsM9QkVXeg6zCQ3Eps2NZMu_PcGWwVXl8P3ceBcxk4FvxIC8JpzriSA03tsitYpxwEQnJX7bCyM0akUAAf_mIHDP6btiE1j_BhqOEgtUB2zkRRKASKO2cVT3SySTCR-VSaZTF5o3dclxZ98U_tAPcUTdlT5JtJ0dyfs7e72dfaQzp_vH2fZPC2kNX0aPGHQlTJFVXljTRBo0AVE6YMGJ4MTaCWSLY32UBaam4qUsKWQrhqAmrDLbe-6az83FPt8WceCmsavqN3E3IGSEhzqwTzbmZuwpDJfd_XSd1_577BBON8KC9-9U5dTaNtFjNTVFPPtP9U3dDFceA</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Clemens, Roger A.</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20110101</creationdate><title>Milk A1 and A2 Peptides and Diabetes</title><author>Clemens, Roger A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c276t-bae9b4f36cffa676b19698b992ab4582b819729e7d64a5dc406fe317d128f7293</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Caseins - genetics</topic><topic>Caseins - immunology</topic><topic>Cattle</topic><topic>Chapter</topic><topic>Diabetes Mellitus, Type 1 - etiology</topic><topic>Genetic Variation</topic><topic>Humans</topic><topic>Milk - adverse effects</topic><topic>Milk - chemistry</topic><topic>Milk - immunology</topic><topic>Peptide Fragments - genetics</topic><topic>Peptide Fragments - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clemens, Roger A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clemens, Roger A.</au><au>Michaelsen KF</au><au>Hernell O</au><au>Clemens RA</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>Milk A1 and A2 Peptides and Diabetes</atitle><btitle>Nestle Nutrition workshop series. Paediatric programme</btitle><addtitle>Nestle Nutr Workshop Ser Pediatr Program</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>67</volume><spage>187</spage><epage>195</epage><pages>187-195</pages><issn>1664-2147</issn><eissn>1664-2155</eissn><eissn>1662-3878</eissn><isbn>9783805595865</isbn><isbn>3805595867</isbn><eisbn>9783805595872</eisbn><eisbn>3805595875</eisbn><abstract>Food-derived peptides, specifically those derived from milk, may adversely affect health by increasing the risk of insulin-dependent diabetes. This position is based on the relationship of type 1 diabetes (T1D) and the consumption of variants A1 and B β-casein from cow’s milk. It appears that β-casomorphin-7 (BCM-7) from β-casein may function as an immunosuppressant and impair tolerance to dietary antigens in the gut immune system, which, in turn, may contribute to the onset of T1D. There are thirteen genetic variants of β-casein in dairy cattle. Among those variants are A1, A2, and B, which are also found in human milk. The amino acid sequences of β-casomorphins among these bovine variants and those found in human milk are similar, often differing only by a single amino acid. In vitro studies indicate BCM-7 can be produced from A1 and B during typical digestive processes; however, BCM-7 is not a product of A2 digestion. Evidence from several epidemiological studies and animal models does not support the association of milk proteins, even proteins in breast milk, and the development of T1D. Ecological data, primarily based on A1/ A2 variations among livestock breeds, do not demonstrate causation, even among countries where there is considerable dairy consumption.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>21335999</pmid><doi>10.1159/000325584</doi><tpages>9</tpages></addata></record> |
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identifier | ISSN: 1664-2147 |
ispartof | Nestle Nutrition workshop series. Paediatric programme, 2011, Vol.67, p.187-195 |
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language | eng |
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source | MEDLINE; Karger Book Series |
subjects | Animals Caseins - genetics Caseins - immunology Cattle Chapter Diabetes Mellitus, Type 1 - etiology Genetic Variation Humans Milk - adverse effects Milk - chemistry Milk - immunology Peptide Fragments - genetics Peptide Fragments - immunology |
title | Milk A1 and A2 Peptides and Diabetes |
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