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dc.contributor.authorAltun, İlayda
dc.contributor.authorKıykım, Ayça
dc.contributor.authorZubarioğlu, Tanyel
dc.contributor.authorBürtecene, Nihan
dc.contributor.authorHopurcuoglu, Duhan
dc.contributor.authorTopcu, Birol
dc.contributor.authorZeybek, Ayşe Çiğdem Aktuğlu
dc.date.accessioned2023-04-20T08:01:12Z
dc.date.available2023-04-20T08:01:12Z
dc.date.issued2022
dc.identifier.issn1328-8067
dc.identifier.issn1442-200X
dc.identifier.urihttps://doi.org/10.1111/ped.15082
dc.identifier.urihttps://hdl.handle.net/20.500.11776/10791
dc.description.abstractBackground Most patients with organic acidemia suffer from recurrent infections. Although neutropenia has been reported in multiple studies, other components of the immune system have not been evaluated thoroughly. This study was conducted to assess the immune status of patients with organic acidemia (OA). Methods Thirty-three patients with OA who were followed up in Istanbul University-Cerrahpasa, Cerrahpasa School of Medicine, Nutrition and Metabolism Department and a total of 32 age- and sex-matched healthy controls were enrolled to the study. The demographic and clinical data were recorded retrospectively from patient files. Complete blood counts, immunoglobulins, and lymphocyte immunophenotyping were recorded prospectively in a symptom- (infection-) free period. Results Of the 33 patients enrolled to the study, 21 (88%) were diagnosed with methylmalonic acidemia, 10 (33%) with propionic acidemia, and two (6.6%) with isovaleric acidemia. The mean age of the patients with OA and healthy subjects were 5.89 +/- 4.11 years and 5.34 +/- 4.36, respectively (P = 0.602). Twenty-nine (88%) of the patients had experienced frequent hospital admission, 13 (39%) were admitted to pediatric intensive care unit, and 18 (55%) suffered from sepsis. Naive helper T cells and recent thymic emigrants were significantly lower in OAs (P < 0.001). Various defects in humoral immunity have also been documented including memory B cells and immunoglobulins. Conclusions Patients with OAs may show adaptive immune defects rendering them susceptible to infections. Metabolic reprogramming based on nutritional modifications may be a promising therapeutic option in the future.en_US
dc.description.sponsorshipResearch Fund of Istanbul University-Cerrahpasa [TSA-2019-33755]; Turkish Pediatric Association [14.02.2019/18]en_US
dc.description.sponsorshipThis work was supported by the Research Fund of Istanbul University-Cerrahpasa (Project number: TSA-2019-33755) and Turkish Pediatric Association (Project number: 14.02.2019/18).en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.identifier.doi10.1111/ped.15082
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectImmune Deficiencyen_US
dc.subjectLymphocyte Metabolismen_US
dc.subjectLymphocyte Subseten_US
dc.subjectOrganic Acidemiaen_US
dc.subjectRecent Thymic Emigranten_US
dc.subjectMethylmalonic Aciduriaen_US
dc.subjectIn-Vitroen_US
dc.subjectPatienten_US
dc.subjectInhibitionen_US
dc.titleAltered immune response in organic acidemiaen_US
dc.typearticleen_US
dc.relation.ispartofPediatrics Internationalen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Biyoistatistik Ana Bilim Dalıen_US
dc.authoridZeybek, Ayse Cigdem Aktuglu/0000-0001-7256-0750
dc.authoridKIYKIM, Ertugrul/0000-0001-5170-5594
dc.authoridcokugras, Haluk Cezmi/0000-0002-0086-3936
dc.authoridKiykim, Ayca/0000-0001-5821-3963
dc.authoridHOPURCUOGLU, Duhan/0000-0001-8599-8284
dc.authoridTopcu, Birol/0000-0003-0771-2505
dc.authoridZubarioglu, Tanyel/0000-0002-7159-4008
dc.identifier.volume64en_US
dc.identifier.issue1en_US
dc.institutionauthorTopcu, Birol
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57221539199
dc.authorscopusid55537270400
dc.authorscopusid56451085500
dc.authorscopusid57756396600
dc.authorscopusid57204543961
dc.authorscopusid37058172000
dc.authorscopusid8283704400
dc.authorwosidZeybek, Ayse Cigdem Aktuglu/C-9812-2019
dc.authorwosidKIYKIM, Ertugrul/ABA-9964-2020
dc.authorwosidKiykim, Ayca/J-6400-2017
dc.identifier.wosWOS:000811136200001en_US
dc.identifier.scopus2-s2.0-85132451704en_US
dc.identifier.pmid34861062en_US


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