Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood
Cell kinetics in the proximal jejunal epithelium were studied by the methods of Cairnie et al. and Wright et al. Seventeen children with untreated malabsorption syndrome and cow's milk protein intolerance (CMI) and 12 of these on a cow's milk free diet were compared with 47 children with u...
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Veröffentlicht in: | Gut 1980-12, Vol.21 (12), p.1041-1046 |
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description | Cell kinetics in the proximal jejunal epithelium were studied by the methods of Cairnie et al. and Wright et al. Seventeen children with untreated malabsorption syndrome and cow's milk protein intolerance (CMI) and 12 of these on a cow's milk free diet were compared with 47 children with untreated coeliac disease, with 15 of these on a gluten free diet, and with 15 controls. The total number of cells in the crypts of the patients with CMI was 1.8 times (P less than 0.001) and in patients with coeliac disease 2.4 times (P less than 0.001) that seen in the controls. During the elimination diet the total number of cells in the crypts returned to the level seen in the controls. The mitotic indices, both crude and corrected, were significantly higher (P less than 0.001) in untreated patients with CMI and those with coeliac disease than in the controls. During dietary treatment the indices fell, but not quite to the level of the controls. These small differences between the two groups may be due to the difference in the causative agents or to the different ages of the patients. |
doi_str_mv | 10.1136/gut.21.12.1041 |
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Seventeen children with untreated malabsorption syndrome and cow's milk protein intolerance (CMI) and 12 of these on a cow's milk free diet were compared with 47 children with untreated coeliac disease, with 15 of these on a gluten free diet, and with 15 controls. The total number of cells in the crypts of the patients with CMI was 1.8 times (P less than 0.001) and in patients with coeliac disease 2.4 times (P less than 0.001) that seen in the controls. During the elimination diet the total number of cells in the crypts returned to the level seen in the controls. The mitotic indices, both crude and corrected, were significantly higher (P less than 0.001) in untreated patients with CMI and those with coeliac disease than in the controls. During dietary treatment the indices fell, but not quite to the level of the controls. These small differences between the two groups may be due to the difference in the causative agents or to the different ages of the patients.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>EISSN: 1458-3288</identifier><identifier>DOI: 10.1136/gut.21.12.1041</identifier><identifier>PMID: 7193162</identifier><identifier>CODEN: GUTTAK</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject>Adolescent ; Adult ; Animals ; Cattle ; Celiac Disease - diet therapy ; Celiac Disease - pathology ; Cell Count ; Cell Differentiation ; Child ; Child, Preschool ; Epithelium - pathology ; Female ; Humans ; Infant ; Intestinal Mucosa - pathology ; Jejunum - pathology ; Malabsorption Syndromes - diet therapy ; Malabsorption Syndromes - pathology ; Male ; Milk Proteins ; Mitotic Index</subject><ispartof>Gut, 1980-12, Vol.21 (12), p.1041-1046</ispartof><rights>Copyright BMJ Publishing Group LTD Dec 1980</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b4001-f2bc10f792784ccd44f3a84c7d146e51f0db45df4d1e02d54f5a01e02e4f69a13</citedby><cites>FETCH-LOGICAL-b4001-f2bc10f792784ccd44f3a84c7d146e51f0db45df4d1e02d54f5a01e02e4f69a13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1419399/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1419399/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7193162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kosnai, I</creatorcontrib><creatorcontrib>Kuitunen, P</creatorcontrib><creatorcontrib>Savilahti, E</creatorcontrib><creatorcontrib>Rapola, J</creatorcontrib><creatorcontrib>Köhegyi, J</creatorcontrib><title>Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood</title><title>Gut</title><addtitle>Gut</addtitle><description>Cell kinetics in the proximal jejunal epithelium were studied by the methods of Cairnie et al. and Wright et al. Seventeen children with untreated malabsorption syndrome and cow's milk protein intolerance (CMI) and 12 of these on a cow's milk free diet were compared with 47 children with untreated coeliac disease, with 15 of these on a gluten free diet, and with 15 controls. The total number of cells in the crypts of the patients with CMI was 1.8 times (P less than 0.001) and in patients with coeliac disease 2.4 times (P less than 0.001) that seen in the controls. During the elimination diet the total number of cells in the crypts returned to the level seen in the controls. The mitotic indices, both crude and corrected, were significantly higher (P less than 0.001) in untreated patients with CMI and those with coeliac disease than in the controls. During dietary treatment the indices fell, but not quite to the level of the controls. These small differences between the two groups may be due to the difference in the causative agents or to the different ages of the patients.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Cattle</subject><subject>Celiac Disease - diet therapy</subject><subject>Celiac Disease - pathology</subject><subject>Cell Count</subject><subject>Cell Differentiation</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Epithelium - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Intestinal Mucosa - pathology</subject><subject>Jejunum - pathology</subject><subject>Malabsorption Syndromes - diet therapy</subject><subject>Malabsorption Syndromes - pathology</subject><subject>Male</subject><subject>Milk Proteins</subject><subject>Mitotic Index</subject><issn>0017-5749</issn><issn>1468-3288</issn><issn>1458-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkUGP0zAQhSMEWpaFKzckS0ggDikex4mTCxKq2AVpCwdgr5ZjT7ZuEztrJyz9FfxlXLWqgAsnj_w-v_HMy7LnQBcARfX2dp4WDBbAFkA5PMjOgVd1XrC6fpidUwoiLwVvHmdPYtxQSuu6gbPsTEBTQMXOs19L7HuytQ4nqyOxjkxrJBvczE71RIfdOBEcbbrs7Tzs9UH1qo0-jJP1jsSdM8EPSO4TQ7S_fx3JYPstGYOfMOHWTb7HoJxGopzZO2ifzJQmxkZUEYnviF7b3qy9N0-zR53qIz47nhfZ98sP35Yf8-svV5-W76_zlqeh8o61GmgnGiZqrrXhvCtUqoRJ42MJHTUtL03HDSBlpuRdqei-RN5VjYLiInt38B3ndkCj0U1B9XIMdlBhJ72y8m_F2bW89T8k8LS6pkkGr44Gwd_NGCc52KjTMpVDP0cpSs54I6oEvvwH3Pg5pO1GCUJQynkBLFGLA6WDjzFgd_oKULkPWqagJQMJTO6DTg9e_DnACT8mm_T8oNs44c-TrMJWVqIQpfx8s5SrK1hd3vCvcpX4Nwe-HTb_6_0bG7bD9A</recordid><startdate>19801201</startdate><enddate>19801201</enddate><creator>Kosnai, I</creator><creator>Kuitunen, P</creator><creator>Savilahti, E</creator><creator>Rapola, J</creator><creator>Köhegyi, J</creator><general>BMJ Publishing Group Ltd and British Society of Gastroenterology</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19801201</creationdate><title>Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood</title><author>Kosnai, I ; Kuitunen, P ; Savilahti, E ; Rapola, J ; Köhegyi, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b4001-f2bc10f792784ccd44f3a84c7d146e51f0db45df4d1e02d54f5a01e02e4f69a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Animals</topic><topic>Cattle</topic><topic>Celiac Disease - diet therapy</topic><topic>Celiac Disease - pathology</topic><topic>Cell Count</topic><topic>Cell Differentiation</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Epithelium - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Intestinal Mucosa - pathology</topic><topic>Jejunum - pathology</topic><topic>Malabsorption Syndromes - diet therapy</topic><topic>Malabsorption Syndromes - pathology</topic><topic>Male</topic><topic>Milk Proteins</topic><topic>Mitotic Index</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kosnai, I</creatorcontrib><creatorcontrib>Kuitunen, P</creatorcontrib><creatorcontrib>Savilahti, E</creatorcontrib><creatorcontrib>Rapola, J</creatorcontrib><creatorcontrib>Köhegyi, J</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kosnai, I</au><au>Kuitunen, P</au><au>Savilahti, E</au><au>Rapola, J</au><au>Köhegyi, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood</atitle><jtitle>Gut</jtitle><addtitle>Gut</addtitle><date>1980-12-01</date><risdate>1980</risdate><volume>21</volume><issue>12</issue><spage>1041</spage><epage>1046</epage><pages>1041-1046</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><eissn>1458-3288</eissn><coden>GUTTAK</coden><abstract>Cell kinetics in the proximal jejunal epithelium were studied by the methods of Cairnie et al. and Wright et al. Seventeen children with untreated malabsorption syndrome and cow's milk protein intolerance (CMI) and 12 of these on a cow's milk free diet were compared with 47 children with untreated coeliac disease, with 15 of these on a gluten free diet, and with 15 controls. The total number of cells in the crypts of the patients with CMI was 1.8 times (P less than 0.001) and in patients with coeliac disease 2.4 times (P less than 0.001) that seen in the controls. During the elimination diet the total number of cells in the crypts returned to the level seen in the controls. The mitotic indices, both crude and corrected, were significantly higher (P less than 0.001) in untreated patients with CMI and those with coeliac disease than in the controls. During dietary treatment the indices fell, but not quite to the level of the controls. These small differences between the two groups may be due to the difference in the causative agents or to the different ages of the patients.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and British Society of Gastroenterology</pub><pmid>7193162</pmid><doi>10.1136/gut.21.12.1041</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Animals Cattle Celiac Disease - diet therapy Celiac Disease - pathology Cell Count Cell Differentiation Child Child, Preschool Epithelium - pathology Female Humans Infant Intestinal Mucosa - pathology Jejunum - pathology Malabsorption Syndromes - diet therapy Malabsorption Syndromes - pathology Male Milk Proteins Mitotic Index |
title | Cell kinetics in the jejunal crypt epithelium in malabsorption syndrome with cow's milk protein intolerance and in coeliac disease of childhood |
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