Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/49366
Campo DC Valoridioma
dc.contributor.authorPozo-Rubio, Tamaraen_US
dc.contributor.authorCapilla, Amaliaen_US
dc.contributor.authorMujico, Jorge R.en_US
dc.contributor.authorDe Palma, Giadaen_US
dc.contributor.authorMarcos, Ascensiónen_US
dc.contributor.authorSanz, Yolandaen_US
dc.contributor.authorPolanco, Isabelen_US
dc.contributor.authorGarcía-Novo, Maria Doloresen_US
dc.contributor.authorCastillejo, Gemmaen_US
dc.contributor.authorRibes-Koninckx, Carmenen_US
dc.contributor.authorVarea, Vicenteen_US
dc.contributor.authorPalau, Francescen_US
dc.contributor.authorOrtigosa, Luisen_US
dc.contributor.authorPeña-Quintana, Luisen_US
dc.contributor.authorNova, Estheren_US
dc.date.accessioned2018-11-24T06:46:42Z-
dc.date.available2018-11-24T06:46:42Z-
dc.date.issued2013en_US
dc.identifier.issn1436-6207en_US
dc.identifier.urihttp://hdl.handle.net/10553/49366-
dc.description.abstractIn addition to genetic risk, environmental factors might influence coeliac disease (CD) development. We sought to assess the effect of the interaction between milk-feeding practices and the HLA-DQ genotype on peripheral lymphocyte subsets and their activation markers in infants at familial risk for CD.170 newborns were classified in 3 different genetic risk groups (high risk, HR; intermediate risk, IR; and low risk, LR) after DQB1 and DQA1 typing. Lymphocyte subsets were studied at the age of 4 months by flow cytometry analysis.79 infants were receiving exclusive breastfeeding (BF) and 91 partial breastfeeding or formula feeding (FF). Regarding genetic risk, 40 infants were classified in HR group, 75 in IR group and 55 in LR group. Two-way ANOVA did not show significant interactions between the type of milk feeding and genetic risk group on the lymphocyte subsets analysed. One-way ANOVA for milk-feeding practice alone showed that the percentage of CD4 + CD25+ cells was significantly higher in BF group than in FF group (BF, 10.92 +/- A 2.71; FF, 9.94 +/- A 2.96; p = 0.026), and absolute counts of CD4 + CD38+ cells were significantly higher in FF group than in BF group (FF, 2,881.23 +/- A 973.48; BF, 2,557.95 +/- A 977.06; p = 0.038). One-way ANOVA for genetic risk alone showed that absolute counts of NK cells were significantly higher in IR group than HR and LR groups (IR, 539.24 +/- A 340.63; HR, 405.01 +/- A 239.53; LR, 419.86 +/- A 262.85; p = 0.028).Lymphocyte subset profiles in the early stages of life could be modulated by milk-feeding practices and genetic risk separately. Breastfeeding might have a positive immunomodulatory effect on lymphocyte subsets in infants at risk of CD.en_US
dc.languageengen_US
dc.relation.ispartofEuropean Journal of Nutritionen_US
dc.sourceEuropean Journal of Nutrition[ISSN 1436-6207],v. 52, p. 637-646 (Marzo 2013)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320110 Pediatríaen_US
dc.subject3206 Ciencias de la nutriciónen_US
dc.subject.otherHuman-Milken_US
dc.subject.otherT-Lymphocyteen_US
dc.subject.otherRotavirus Infectionen_US
dc.subject.otherHealthy-Childrenen_US
dc.subject.otherGenetic Risken_US
dc.subject.other1St Yearen_US
dc.subject.otherSubpopulationsen_US
dc.subject.otherAutoimmunityen_US
dc.subject.otherGliadinen_US
dc.subject.otherTermen_US
dc.titleInfluence of breastfeeding versus formula feeding on lymphocyte subsets in infants at risk of coeliac disease: The PROFICEL studyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00394-012-0367-8en_US
dc.identifier.scopus84879553949-
dc.identifier.isi000314970600021-
dc.contributor.authorscopusid54395982600-
dc.contributor.authorscopusid20435263900-
dc.contributor.authorscopusid13102653200-
dc.contributor.authorscopusid26029304200-
dc.contributor.authorscopusid7102096885-
dc.contributor.authorscopusid7003409923-
dc.contributor.authorscopusid7003796886-
dc.contributor.authorscopusid6604061266-
dc.contributor.authorscopusid57205046996-
dc.contributor.authorscopusid14631687000-
dc.contributor.authorscopusid6602108756-
dc.contributor.authorscopusid35516564800-
dc.contributor.authorscopusid7006313852-
dc.contributor.authorscopusid54946469200-
dc.contributor.authorscopusid6603266503-
dc.contributor.authorscopusid6602087177-
dc.description.lastpage646en_US
dc.description.firstpage637en_US
dc.relation.volume52en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid3988295-
dc.contributor.daisngid1927783-
dc.contributor.daisngid2557614-
dc.contributor.daisngid1012638-
dc.contributor.daisngid10207-
dc.contributor.daisngid5966-
dc.contributor.daisngid275018-
dc.contributor.daisngid10313586-
dc.contributor.daisngid1170900-
dc.contributor.daisngid629698-
dc.contributor.daisngid631701-
dc.contributor.daisngid150667-
dc.contributor.daisngid1113114-
dc.contributor.daisngid1012004-
dc.contributor.daisngid441276-
dc.description.numberofpages10en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Pozo-Rubio, T-
dc.contributor.wosstandardWOS:Capilla, A-
dc.contributor.wosstandardWOS:Mujico, JR-
dc.contributor.wosstandardWOS:de Palma, G-
dc.contributor.wosstandardWOS:Marcos, A-
dc.contributor.wosstandardWOS:Sanz, Y-
dc.contributor.wosstandardWOS:Polanco, I-
dc.contributor.wosstandardWOS:Garcia-Novo, MD-
dc.contributor.wosstandardWOS:Castillejo, G-
dc.contributor.wosstandardWOS:Ribes-Koninckx, C-
dc.contributor.wosstandardWOS:Varea, V-
dc.contributor.wosstandardWOS:Palau, F-
dc.contributor.wosstandardWOS:Ortigosa, L-
dc.contributor.wosstandardWOS:Pena-Quintana, L-
dc.contributor.wosstandardWOS:Nova, E-
dc.date.coverdateMarzo 2013en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,021-
dc.description.jcr3,84-
dc.description.sjrqQ1-
dc.description.jcrqQ1-
dc.description.scieSCIE-
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Nutrición-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0001-6052-5894-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNamePeña Quintana, Luis-
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