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        <identifier>oai:hull-repository.worktribe.com:4192858</identifier>
        <datestamp>2025-10-09T10:51:13Z</datestamp>
        <setSpec>084104101115105115</setSpec>
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        <uketd_dc:uketddc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:uketd_dc="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/" xmlns:uketdterms="http://naca.central.cranfield.ac.uk/ethos-oai/terms/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:type>Thesis</dc:type>
          <dc:title>Association of Differing Qatari Genotypes with Vitamin D Metabolites</dc:title>
          <dcterms:abstract>This work aimed to determine the possible association between Qatari genotypes and vitamin-D deficiency and diabetes complications. Through next-generation exome sequencing three major genetic Qatari genotypes were determined, Q1 - Bedouin, Q2 - Persian-South Asian and Q3 - African. The hypothesis was that Qatari genotypes would affect vitamin D and metabolite levels independent of cultural factors, perhaps exacerbated by diabetes.Materials and Methods. Affymetrix 500k SNP arrays determined 398 Qataris genotype (mean age 49.8 years, 56.8% male; type 2 diabetes (T2DM) 220; control 178). LC-MS/MS analysis measured 1,25-dihydroxyvitamin-D (1,25(OH)2D), 25-hydroxyvitamin-D2 (25(OH)D2), 25-hydroxyvitamin-D3 (25(OH)D3), 24,25-dihydroxyvitamin-D (24,25(OH)2D) and 25-hydroxy-3epi-Vitamin-D (3epi25(OH)D). The same study population was used to investigate the association of diabetes and its complications with various genotypes.Results. There was no difference in 25(OH)D levels between genotype groups; however, 1,25(OH)2D was higher for Q2 and 24,25(OH)2D was higher in Q1 compared to the ‘admixed’ group. Additionally, the genotype-based ancestry and type 2 diabetes (T2DM) prevalence: 164 (41.2%) with Q1, 60.4% with T2DM; 149 (37.4%) with Q2, 49.7% with T2DM; 31 (7.8%) with Q3, 61.3% with T2DM; and 54 (13.6%) with “admixed”, 51.9% with T2DM. In patients with diabetes, hypertension (p&lt;0.035) and retinopathy (p&lt;0.016) were greater in Q3.Conclusion. Overall, the study population was vitamin-D deficient, total 25(OH)D was higher in patients with concomitant T2DM, 1,25(OH)2D, 24,25(OH)2D and 3epi25(OH)D were lower in diabetes. Vitamin D levels were not associated with a specific genotype. Q3 was found to have a higher frequency of diabetic retinopathy and hypertension.</dcterms:abstract>
          <dc:creator>Dakroury, Youssra</dc:creator>
          <uketdterms:qualificationname>MSc</uketdterms:qualificationname>
          <uketdterms:qualificationlevel>Masters</uketdterms:qualificationlevel>
          <dcterms:dateAccepted>2020-11-01</dcterms:dateAccepted>
          <uketdterms:institution>Hull York Medical School, The University of Hull and The University of York</uketdterms:institution>
          <dc:identifier>oai:hull-repository.worktribe.com:4192858</dc:identifier>
          <dc:identifier xsi:type="dcterms:URI">https://hull-repository.worktribe.com/4192858/1/Thesis</dc:identifier>
          <uketdterms:sponsor>University of Hull</uketdterms:sponsor>
          <dcterms:isReferencedBy>https://hull-repository.worktribe.com/output/4192858</dcterms:isReferencedBy>
          <dcterms:issued>2020</dcterms:issued>
          <dc:language>en</dc:language>
          <dc:licence>openAccess</dc:licence>
          <dcterms:accessRights>Public</dcterms:accessRights>
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