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dc.contributor.authorAYDIN, Merve
dc.contributor.authorYAZICI, Mustafa
dc.contributor.authorDEMİRKAZIK, Mehtap
dc.contributor.authorKOLTAŞ, İsmail Soner
dc.contributor.authorÇIKMAN, Aytekin
dc.contributor.authorGÜLHAN, Barış
dc.contributor.authorDURAN, Tuğçe
dc.contributor.authorYILMAZ, Aysun
dc.contributor.authorKARA, Murat
dc.date.accessioned2020-01-17T08:41:47Z
dc.date.available2020-01-17T08:41:47Z
dc.date.issued2019-10-30
dc.identifier.issn1995-7645
dc.identifier.urihttp://hdl.handle.net/20.500.12498/1638
dc.description.abstractObjective: To investigate Blastocystis’ etiologic role and association with gastrointestinal symptomatology in acute and chronic urticaria patients and to identify Blastocystis subtypes responsible for urticaria. Methods: The study included urticaria patients and healthy individuals that presented to our polyclinic between June 2015 and May 2017. The participants were assigned into Group I (137 patients), subdivided into acute (72) and chronic urticaria patients (65), and Group II (129 control individuals). Blastocystis presence was investigated by native-Lugol examination, trichrome staining, PCR using sequence tagged site primers, and DNA sequencing analysis. The phylogenetic tree was constructed. Results: The native-Lugol and trichrome staining methods revealed that 16 patients (16/133, 12.0%) had Blastocystis-positive stool samples, of which seven samples (7/133, 5.3%) belonged acute and nine (9/133, 6.8%) to chronic urticaria patients. Concerning Blastocystis subtypes, of the acute urticaria patients, three had subtype 1 (ST1), one had ST2, and three had ST3. Of the chronic urticaria patients, one had ST1 and eight had ST3. Blastocystis positivity was detected in two control individuals (2/123, 1.6%), both being ST3. All subtypes identified by PCR were confirmed by the sequencing analysis. The acute and chronic urticaria groups showed no statistically significant differences for Blastocystis positivity (P=0.60) and subtype distribution (P=0.15). A statistically significant difference was found between the urticaria patients and the controls for Blastocystis positivity (P<0.01), but not for subtype distribution (P=0.67) or for Blastocystis presence and gastrointestinal complaints. Conclusions: This study on Blastocystis subtype distribution among Turkish urticaria patients showed results consistent with the literature. It was concluded that Blastocystis should be kept in mind in patients with urticariaen_US
dc.description.sponsorshipThis project was financially supported by the Scientific Project Unit of Erzincan University (Project No: SAG-A-240215-0128).en_US
dc.language.isoenen_US
dc.publisherAsian Pacific Journal of Tropical Medicineen_US
dc.subjectUrticariaen_US
dc.subjectBlastocystisen_US
dc.subjectSubtypesen_US
dc.subjectPCRen_US
dc.subjectDNA Sequence Analysisen_US
dc.titleMolecular characterization and subtyping of Blastocystis in urticarial patients in Turkeyen_US
dc.typeMakaleen_US


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