The genetic map of diabetic nephropathy: Evidence from a systematic review and meta-analysis of genetic association studies

التفاصيل البيبلوغرافية
العنوان: The genetic map of diabetic nephropathy: Evidence from a systematic review and meta-analysis of genetic association studies
المؤلفون: Tziastoudi M., Stefanidis I., Zintzaras E.
المصدر: Clinical Kidney Journal ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85101071282&doi=10.1093%2fCKJ%2fSFAA077&partnerID=40&md5=4be420d2eed87aba3f0c969a2e7f988cTest
سنة النشر: 2020
المجموعة: University of Thessaly Institutional Repository / Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
مصطلحات موضوعية: 5,10 methylenetetrahydrofolate reductase (FADH2), acetyl coenzyme A carboxylase, acetyl coenzyme A carboxylase beta, adipocytokine, adiponectin, apolipoprotein E, carnosine dipeptidase 1, chemokine receptor CCR5, dipeptidyl carboxypeptidase, endothelial nitric oxide synthase, engulfment and cell motility 1 protein, glucose transporter 1, glucose transporter 2, high mobility group A2 protein, histone lysine methyltransferase, interleukin 10, interleukin 1beta, interleukin 8, potassium channel KCNQ1, pyruvic acid, SET domain containing 7 histone lysine methyltransferase, sirtuin 1, sodium chloride cotransporter, somatomedin B, tissue inhibitor of metalloproteinase 1, transcription factor 7 like 2, transforming growth factor beta1, unclassified drug, vasculotropin A, vasculotropin receptor 3
الوصف: Despite the extensive efforts of scientists, the genetic background of diabetic nephropathy (DN) has not yet been clarified. To elucidate the genetic variants that predispose to the development of DN, we conducted a systematic review and meta-analysis of all available genetic association studies (GAS) of DN. We searched in the Human Genome Epidemiology Navigator (HuGE Navigator) and PubMed for available GAS of DN. The threshold for meta-analysis was three studies per genetic variant. The association between genotype distribution and DN was examined using the generalized linear odds ratio (ORG). For variants with available allele frequencies, the examined model was the allele contrast. The pooled OR was estimated using the DerSimonian and Laird random effects model. The publication bias was assessed with Egger's test. We performed pathway analysis of significant genes with DAVID 6.7. Genetic data of 606 variants located in 228 genes were retrieved from 360 GASs and were synthesized with meta-analytic methods. ACACB, angiotensin I-converting enzyme (ACE), ADIPOQ, AGT, AGTR1, AKR1B1, APOC1, APOE, ATP1B2, ATP2A3, CARS, CCR5, CGNL1, Carnosine dipeptidase 1 (CNDP1), CYGB-PRCD, EDN1, Engulfment and cell motility 1 (ELMO1), ENPP1, EPO, FLT4, FTO, GLO1, HMGA2, IGF2/INS/TH cluster, interleukin 1B (IL1B), IL8, IL10, KCNQ1, KNG, LOC101927627, Methylenetetrahydrofolate reductase, nitric oxide synthase 3 (NOS3), SET domain containing seven, histone lysine methyltransferase (SETD7), Sirtuin 1 (SIRT1), SLC2A1, SLC2A2, SLC12A3, SLC19A3, TCF7L2, TGFB1, TIMP1, TTC39C, UNC13B, VEGFA, WTAPP1, WWC1 as well as XYLT1 and three intergenic polymorphisms showed significant association with DN. Pathway analysis revealed the overrepresentation of six signalling pathways.The significant findings provide further evidence for genetic factors implication in DN offering new perspectives in discovery of new therapies. © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. This is an Open Access article distributed under ...
نوع الوثيقة: other/unknown material
اللغة: English
تدمد: 20488505
العلاقة: http://hdl.handle.net/11615/80246Test
DOI: 10.1093/CKJ/SFAA077
الإتاحة: https://doi.org/10.1093/CKJ/SFAA077Test
http://hdl.handle.net/11615/80246Test
رقم الانضمام: edsbas.3FE381C9
قاعدة البيانات: BASE
الوصف
تدمد:20488505
DOI:10.1093/CKJ/SFAA077