Association of rs6259 polymorphism with SHBG levels and Poly Cystic Ovary Syndrome in Indian population : a case control study

Polycystic ovary syndrome (PCOS) is the most common endocrinopathy of reproductive-aged women. PCOS reflects a number of possible etiologies but its pathophysiology is still unclear. The principal abnormality of the syndrome is hyperandrogenism (70-80%). The access of androgens to target tissues is regulated by sex hormone-binding globulin (SHBG), a transport protein secreted by liver i.e. specific for androgens. Present study was done to find the association of rs6259 polymorphism with SHBG levels and Poly Cystic Ovary Syndrome in Indian population. Present study was a case control study. 400 subjects were enrolled for the study and serum SHBG levels and D327N polymorphism were measured. The D327N polymorphism (wild-type and variant allele) was detected using PCR-RFLP method (restriction enzyme Bbs-I). PCOS group was found to have significantly lower SHBG levels than healthy controls. There was no significant difference in genotype distribution between PCOS and controls (χ2 = 1.0335, p = 0.59). Significant difference in SHBG levels of PCOS and control group highlights the potential of SHBG as a biomarker for PCOS. However, no significant difference in genotype distribution between PCOS and controls provided an insight that rs6259 polymorphism is not associated with the risk of PCOS and SHBG levels.

Medienart:

E-Artikel

Erscheinungsjahr:

2019

Erschienen:

2019

Enthalten in:

Zur Gesamtaufnahme - volume:46

Enthalten in:

Molecular biology reports - 46(2019), 2 vom: 04. Apr., Seite 2131-2138

Sprache:

Englisch

Beteiligte Personen:

Bhatnager, Richa [VerfasserIn]
Senwal, Alka [VerfasserIn]
Nanda, Smiti [VerfasserIn]
Dang, Amita S [VerfasserIn]

Links:

Volltext

Themen:

Diagnostic marker
Journal Article
PCOS
Polymorphism
SHBG
SHBG protein, human
Sex Hormone-Binding Globulin
Susceptibility marker

Anmerkungen:

Date Completed 10.09.2019

Date Revised 25.02.2020

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1007/s11033-019-04665-2

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM29346331X