Molecular Medicine II.
Dr. Varhegyi, Vera
ZF3KHN
Semmelweis University, Department of Obstetrics and Gynecology / Semmelweis University, Institute of Genomic Medicine and Rare Disorders
+36206663493
varhegyi.vera@semmelweis.hu
GDF-15 and mtDNA deletions show potential as effective biomarkers for detecting mitochondrial dysfunction in cases of insulin resistance and PCOS
Vera Várhegyi1, Anna Modos1, Domonkos Trager2, Dora Gerszi3, Eszter Maria Horvath4, Miklos Sipos3, Nandor Acs3, Maria Judit Molnar2, Szabolcs Varbiro5, Aniko Gal2
1: Semmelweis University, Institute of Genomic Medicine and Rare Disorders / Semmelweis University, Department of Obstetrics and Gynecology
2: Semmelweis University, Institute of Genomic Medicine and Rare Disorders
3: Semmelweis University, Department of Obstetrics and Gynecology
4: Semmelweis University, Department of Physiology
5: Semmelweis University, Department of Obstetrics and Gynecology / University of Szeged, Albert Szent-Györgyi Health Centre, Department of Obstetrics and Gynecology
Szóbeli
Molecular Medicine II.
Hungarian
Molecular Medicine
Introduction: There is no existing literature regarding the combination of the growth differentiation factor-15 (GDF-15) biomarker and mitochondrial DNA (mtDNA) deletions in insulin resistance (IR), polycystic ovary syndrome (PCOS), and the associated infertility. However, exploring this combination could prove valuable in achieving optimal metabolic health and enhancing pregnancy outcomes.
Aim: This study aimed to investigate the roles of GDF-15 and mtDNA deletions as biomarkers in the pathogenesis of IR and PCOS.
Patients and Methods: A total of 81 female patients diagnosed with IR, PCOS, or both, along with infertility and clinical signs indicating mitochondrial dysfunction, were examined, alongside 41 healthy controls. Blood and urine epithelial cells were isolated for DNA extraction. GDF-15 levels were measured using an ELISA kit, while mtDNA deletions were assessed through long-range PCR.
Results: GDF-15 levels in patients showed a significant elevation compared to controls. Specifically, 12 patients with elevated GDF-15 levels all had a BMI over 25 kg/m2 and exhibited reactive hyperinsulinemia. MtDNA deletions were observed in 61.5% of the patient group, predominantly among those with IR only. The increase in plasma GDF-15 levels and prevalence of mtDNA deletions were directly correlated with BMI. Patients with more pronounced metabolic abnormalities required more intensive drug therapy, leading to a parallel increase in plasma GDF-15 levels.
Conclusion: elevated GDF-15 levels and the presence of mtDNA deletions may stem from carbohydrate metabolism disorders in patients, potentially serving as indicators of an accelerated aging process.
Funding: This study was supported by NKFIH_FK_132812, János Bolyai Research Scholarship, ÚNKP-22-5 Research Scholarship (New National Excellence Program of the Ministry for
Innovation and Technology from the source of the National Research, Development and Innovation Fund) and TKP2021-EGA.25, TKP2021-NVA-15, SE STIA-OTKA-2021 and Hungarian
Society of Hypertension grants.
Semmelweis University
Aniko Gal
I do not give consent to the publication of my abstract on the website of the congress.
Szabad
elfogadva
szóbeli
nem rendelkezett róla
6907
17:15
17:25