Egyszerű nézet

dc.contributor.author Juhasz E
dc.contributor.author Kiss E
dc.contributor.author Simonova E
dc.contributor.author Patócs, Attila Balázs
dc.contributor.author Reismann, Péter
dc.date.accessioned 2016-05-31T10:13:19Z
dc.date.available 2016-05-31T10:13:19Z
dc.date.issued 2016
dc.identifier.citation pagination=22, pages: 6; journalVolume=21; journalIssueNumber=1; journalTitle=EUROPEAN JOURNAL OF MEDICAL RESEARCH;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3419
dc.identifier.uri doi:10.1186/s40001-016-0212-2
dc.description.abstract BACKGROUND: It has been previously postulated that high phenylalanine (Phe) might disturb intracerebral dopamine production, which is the main regulator of prolactin secretion in the pituitary gland. Previously, various associations between Phe and hyperprolactinemia were revealed in studies performed in phenylketonuria (PKU) children and adolescents. The aim of the present study was to clarify whether any relation between serum phenylalanine and prolactin levels can be found in adult PKU patients. PATIENTS AND METHODS: We conducted a cross-sectional, monocentric study including 158 adult patients (male n = 68, female n = 90) with PKU. All patients were diagnosed during newborn screening and were treated since birth. Serum Phe, tyrosine (Tyr), prolactin (PRL), and thyroid-stimulating hormone (TSH) levels were measured, and Phe/Tyr ratio was calculated. Males and females were analyzed separately because the serum prolactin level is gender-dependent. RESULTS: No significant correlations were found between serum phenylalanine, tyrosine, or the Phe/Tyr ratio and serum prolactin level either in the male or in the female group. CONCLUSIONS: In treated adult PKU patients, the serum prolactin level may not be significantly influenced by Phe or Tyr serum levels.
dc.relation.ispartof urn:issn:0949-2321
dc.title Serum prolactin as a biomarker for the study of intracerebral dopamine effect in adult patients with phenylketonuria: a cross-sectional monocentric study
dc.type Journal Article
dc.date.updated 2016-05-31T09:51:34Z
dc.language.rfc3066 en
dc.identifier.mtmt 3072017
dc.identifier.pubmed 27169416
dc.contributor.department SE/AOK/K/IISZBK/MTA-SE Lendület Örökletes Endokrin Daganatok Kutatócsoport
dc.contributor.department SE/AOK/K/II. Sz. Belgyógyászati Klinika
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote PMC PMC4864969


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