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Mitochondrial DNA haplogroups and risk of new-onset diabetes among tacrolimus-treated renal transplanted patients
- Source :
- Gene. 538:195-198
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
Abstract
- Background and aims Tacrolimus (Tac) is an immunosuppressive drug widely used to avoid organ rejection. New-onset diabetes after transplantation (NODAT) is a major complication among transplanted patients who receive Tac. The increased risk for NODAT could be partly mediated by the effect of Tac on mitochondria from pancreatic beta-cells. Common and rare mitochondrial DNA variants have been linked to the risk of diabetes. Our aim was to determine whether mtDNA polymorphisms/haplogroups were associated with NODAT in Tac-treated kidney transplanted. Methods Seven polymorphisms that define the common European haplogroups were determined in 115 NODAT and 197 no-NODAT patients. Results Haplogroup H was significantly more frequent in the NODAT group (50% vs. 35%; p = 0.01, OR = 1.82). There was no difference between patients without and with (n = 106) D2M prior to the transplant. Conclusions Mitochondrial haplogroup H was associated with the risk for NODAT among Tac-treated transplanted patients. The reported differences between the mtDNA variants could explain the increased NODAT-risk among H-patients.
- Subjects :
- Adult
Male
medicine.medical_specialty
Mitochondrial DNA
Adolescent
Haplogroup H
medicine.medical_treatment
Biology
DNA, Mitochondrial
Gastroenterology
Tacrolimus
Haplogroup
Diabetes mellitus
Internal medicine
Genetics
medicine
Humans
Genetic Predisposition to Disease
Aged
Polymorphism, Genetic
General Medicine
Middle Aged
medicine.disease
Kidney Transplantation
Transplantation
Immunosuppressive drug
Diabetes Mellitus, Type 2
Haplotypes
Case-Control Studies
Female
Immunosuppressive Agents
Human mitochondrial DNA haplogroup
Subjects
Details
- ISSN :
- 03781119
- Volume :
- 538
- Database :
- OpenAIRE
- Journal :
- Gene
- Accession number :
- edsair.doi.dedup.....0667dd97e70be99a98237a91b4e98d62
- Full Text :
- https://doi.org/10.1016/j.gene.2014.01.036