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Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution
المؤلفون المشاركون
Mi, Xiao-xiao
Yan, Jian
Ma, Xiao-jie
Zhu, Ge-li
Gao, Yi-dan
Yang, Wen-jun
Kong, Xiao-wen
Chen, Gong-ying
Shi, Jun-ping
Gong, Ling
المصدر
العدد
المجلد 2019، العدد 2019 (31 ديسمبر/كانون الأول 2019)، ص ص. 1-9، 9ص.
الناشر
Hindawi Publishing Corporation
تاريخ النشر
2019-07-29
دولة النشر
مصر
عدد الصفحات
9
التخصصات الرئيسية
الملخص EN
Objective.
The spectrum of UDP-glucuronyl transferase A1 (UGT1A1) variants in hereditary unconjugated hyperbilirubinemia varies markedly between different ethnic populations.
This study evaluated the UGT1A1 genotypes in hyperbilirubinemia patients from southeastern China.
Methods.
We enrolled 60 patients from southeastern China (44 men and 16 women; age range: 3–76 years) with unconjugated hyperbilirubinemia and performed genetic analysis of the UGT1A1 gene by direct sequencing.
Results.
For patients with Gilbert syndrome, 85% (47/55) harbored pathogenic variants of UGT1A1⁎60.
Both UGT1A1⁎28 and UGT1A1⁎81 were detected in the promoter region of UGT1A1.
Additionally, 83% (20/24) of patients with Gilbert syndrome heterozygous for UGT1A1⁎60 had an association with heterozygous variation of UGT1A1⁎28 or UGT1A1⁎81, while 91% (21/23) of Gilbert syndrome patients homozygous for UGT1A1⁎60 had biallelic variations of UGT1A1⁎28 and UGT1A1⁎81.
We detected 213 UGT1A1 allelic variants, including six novel variations, with the most frequent allele being the UGT1A1⁎60, followed by UGT1A1⁎28 and UGT1A1⁎6.
All of the patients showed multiple sites of variants in UGT1A1; however, variation number was not associated with bilirubin levels (P>0.05).
Conclusions.
The spectrum of UGT1A1 variants in southeastern Chinese patients was distinct from other ethnic populations.
Our findings broaden the knowledge concerning traits associated with UGT1A1 variants and help profile genotype–phenotype correlations in hyperbilirubinemia patients.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Mi, Xiao-xiao& Yan, Jian& Ma, Xiao-jie& Zhu, Ge-li& Gao, Yi-dan& Yang, Wen-jun…[et al.]. 2019. Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution. BioMed Research International،Vol. 2019, no. 2019, pp.1-9.
https://search.emarefa.net/detail/BIM-1126588
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Mi, Xiao-xiao…[et al.]. Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution. BioMed Research International No. 2019 (2019), pp.1-9.
https://search.emarefa.net/detail/BIM-1126588
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Mi, Xiao-xiao& Yan, Jian& Ma, Xiao-jie& Zhu, Ge-li& Gao, Yi-dan& Yang, Wen-jun…[et al.]. Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution. BioMed Research International. 2019. Vol. 2019, no. 2019, pp.1-9.
https://search.emarefa.net/detail/BIM-1126588
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-1126588
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
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تقوم هذه الخدمة بالتحقق من التشابه أو الانتحال في الأبحاث والمقالات العلمية والأطروحات الجامعية والكتب والأبحاث باللغة العربية، وتحديد درجة التشابه أو أصالة الأعمال البحثية وحماية ملكيتها الفكرية. تعرف اكثر
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