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Related Experiment Video

Updated: Jun 24, 2026

Chromosomics: Detection of Numerical and Structural Alterations in All 24 Human Chromosomes Simultaneously Using a Novel OctoChrome FISH Assay
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An X-chromosome scan reveals a locus for fat distribution in chromosome region Xp21-22.

R Arlen Price1, Wei-Dong Li, Robin Kilker

  • 1Center for Neurobiology and Behavior, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6140, USA. arlen@bgl.psycha.upenn.edu

Diabetes
|May 29, 2002
PubMed
Summary
This summary is machine-generated.

Researchers investigated the X chromosome for obesity links, finding suggestive evidence for waist-to-hip ratio (WHR) in women. This genetic locus may influence female fat distribution on chromosome Xp21-22.

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Area of Science:

  • Genetics
  • Human Obesity Research
  • Medical Genetics

Background:

  • Previous genome scans for obesity primarily focused on autosomes.
  • Limited research has explored the X chromosome's role in human obesity.
  • Conflicting findings exist regarding X chromosome linkage to obesity phenotypes.

Purpose of the Study:

  • To investigate the X chromosome for quantitative trait loci (QTLs) associated with obesity and related phenotypes.
  • To examine linkage of five obesity phenotypes and two derived traits (leptin resistance, fat patterning) to X chromosome markers.
  • To analyze data from independent European-American and African-American family cohorts.

Main Methods:

  • Genome-wide scan of the X chromosome using 20 markers in 190 European-American and 43 African-American families.
  • Analysis of body mass index (BMI), body fat percentage, hip and waist circumferences, plasma leptin, leptin resistance, and waist-to-hip ratio (WHR).
  • Nonparametric linkage analyses adjusted for age, race, and sex, with suggestive linkage defined by specific Z score thresholds.

Main Results:

  • Suggestive linkage was identified exclusively for WHR, indicating a potential QTL for fat distribution.
  • Linkage signals were detected in both family sets, with stronger evidence in females.
  • The identified linkage region on Xp21-22, while significant, is broad and distinct from previously reported intervals.

Conclusions:

  • A QTL influencing female fat distribution may be located in the Xp21-22 region.
  • The findings support further investigation of the X chromosome in obesity research, particularly in women.
  • Divergent results highlight the need for replication and examination of the X chromosome by other research groups.