Evidence map›Paper›PMID 33641658›Full record

ArticleExperimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation2023

TCF7L2 (rs7903146) But Not CDKAL1 (rs7754840) Gene Polymorphisms Increase the Risk of New-Onset Diabetes After Kidney Transplant.

Özant Helvaci, Berfu Korucu, Haci Hasan Yeter, Sevim Gönen, Burçak Cavnar Helvaci, Yavuz Sanisoğlu, Musa Bali, Galip Güz

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Article in Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed, 3 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Özant HelvaciFrom the Yildirim Beyazit University, Yenimahalle Education and Research Hospital, Ankara, Turkey.
Berfu Korucu
Haci Hasan Yeter
Sevim Gönen
Burçak Cavnar Helvaci
Yavuz Sanisoğlu
Musa Bali
Galip Güz
Ankara Yıldırım Beyazıt University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIncidence of new-onset diabetes after transplant negatively affects graft and patient survival. Obesity, impaired fasting glucose before transplant, and a history of diabetes in first-degree relatives are well-defined risk factors. TCF7L2 and CDKAL1 gene polymorphisms have been implicated in the pathogenesis.We investigated the effect of single gene polymorphisms of TCF7L2 (rs7903146) and CDKAL1 (rs7754840) on new-onset diabetes in renal transplant recipients. MATERIALS AND

methodsWe evaluated 239 renal transplant recipients. TCF7L2 and CDKAL1 gene polymorphisms were assessed by polymerase chain reaction.

resultsMean patient age was 43 ± 13 years. There were 148 male patients (61.9%), and 91 were female (38.1%). New-onset diabetes was detected in 55 patients (23%). In 20 cases (36%), the glycemic disorder was transient; 61% of patients required insulin therapy. In terms of CDKAL1, 108 patients had the wild-type allele, 112 had a single-allele mutation, and 19 had a 2-allele mutation (45.2%, 46.9%, and 7.9%, respectively). In terms of TCF7L2, 163 of the patients had the wild-type allele, 49 had a single-allele mutation, and 27 had a 2-allele mutation (68%, 20%, and 11%, respectively). New-onset diabetes-related factors were age at transplant, body mass index after transplant (calculated as weight in kilograms divided by height in meters squared), tacrolimus, mycophenolate, andTCF7L2 polymorphism but not CDKAL1 polymorphism. After multiple regression analysis, the effect of TCF7L2 polymorphism persisted. A single allelic change resulted in a risk factor 1.4 times higher for new-onset diabetes after transplant (P = .043; 95% CI, 1.142-1.874) and a double allelic change was 2.7 times higher (P < .01; 95% CI, 1.310-4.073).

conclusionsTCF7L2 (rs7903146) gene polymorphism is an independent risk factor for new-onset diabetes in Turkish renal transplant patients. This study is the first in Turkey to show the distribution and effect of these genes in kidney transplant patients.

Indexed as

Diabetes MellitusDiabetes Mellitus, Type 2Kidney TransplantationAdultFemaleGenetic Predisposition to DiseaseGenotypeHumansInsulinMaleMiddle AgedPolymorphism, Single NucleotideRisk FactorsTranscription Factor 7-Like 2 ProteintRNA MethyltransferasesCDKAL1 protein, humanInsulinTCF7L2 protein, humanTranscription Factor 7-Like 2 ProteintRNA Methyltransferases

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PMID33641658
OpenAlexW3134777812

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.