Affiliations 

  • 1 Sh Jahanfar, PhD. Obstetrics and Gynecology, Project Manager, Lecturer Royal College of Medicine, Perak Ipoh, Malaysia, also former Associate Professor, Iran University of Medical Science, Tehran, Iran
  • 2 H Maleki, BSc. Midwifery, Research Assistant, Avecina Research Center, Shahid-Beheshti University
  • 3 A R Mosavi, PhD. Epidemiology, Statistician, Avecina Research Center, Shahid-Beheshti University
Med J Malaysia, 2005 Oct;60(4):441-6.
PMID: 16570705

Abstract

The genetic property of subclinical eating behaviour (SEB) and the link between SEB and polycystic ovary syndrome (PCOS) has been studied before but the role of leptin within this connection has never been investigated. The objective of this study was 1). to study the genetic property of SEB. 2). To find a link between leptin, SEB and PCOS. One hundred and fifty four (77 pairs) female-female Iranian twins including 96 MZ individuals (48 pairs) and 58 DZ individuals (29 pairs) participated in the study. Clinical, biochemical and ultrasound tools were used to diagnose polycystic ovary syndrome. BITE questionnaire was filled out for subjects. Eight percent of subjects were diagnosed for subclinical eating disorder. No significant difference was found between intraclass correlation of MZ and DZ (z = 0.57, P = 0.569). Serum leptin level correlated significantly with bulimia score (P < 0.007). The mean (+/-SD) value for bulimia score was found to be higher among PCOS(positive) subjects (3.27 +/- 5.51) in comparison with PCOS(negative) subjects (2.06 +/- 4.48) (P < 0.001). The genetic property of subclinical eating disorder was not confirmed as shared environment might have played a major role in likeliness of DZ twins as well as MZ. Leptin is linked with both subclinical eating disorder and PCOS.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.