Sex and age specific effects of chromosomal regions linked to body mass index in the Framingham Study
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Published:2006-01-26
Issue:1
Volume:7
Page:
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ISSN:1471-2156
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Container-title:BMC Genetics
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language:en
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Short-container-title:BMC Genet
Author:
Atwood Larry D,Heard-Costa Nancy L,Fox Caroline S,Jaquish Cashell E,Cupples L Adrienne
Abstract
Abstract
Background
Previously, we reported significant linkage of body mass index (BMI) to chromosomes 6 and 11 across six examinations, covering 28 years, of the Framingham Heart Study. These results were on all individuals available at each exam, thus the sample size varied from exam to exam. To remove any effect of sample size variation we have now constructed six subsets; for each exam individuals were only included if they were measured at every exam, i.e. for each exam, included individuals comprise the intersection of the original six exams. This strategy preferentially removed older individuals who died before reaching the sixth exam, thus the intersection datasets are smaller (n = 1114) and significantly younger than the full datasets. We performed variance components linkage analysis on these intersection datasets and on their sex-specific subsets.
Results
Results from the sex-specific genome scans revealed 11 regions in which a sex-specific maximum lodscore was at least 2.0 for at least one dataset. Randomization tests indicated that all 11 regions had significant (p < 0.05) differences in sex-specific maximum lodscores for at least three datasets. The strongest sex-specific linkage was for men on chromosome 16 with maximum lodscores 2.70, 3.00, 3.42, 3.61, 2.56 and 1.93 for datasets 1–6 respectively.
Results from the full genome scans revealed that linked regions on chromosomes 6 and 11 remained significantly and consistently linked in the intersection datasets. Surprisingly, the maximum lodscore on chromosome 10 for dataset 1 increased from 0.97 in the older original dataset to 4.23 in the younger smaller intersection dataset. This difference in maximum lodscores was highly significant (p < 0.0001), implying that the effect of this chromosome may vary with age. Age effects may also exist for the linked regions on chromosomes 6 and 11.
Conclusion
Sex specific effects of chromosomal regions on BMI are common in the Framingham study. Some evidence also exists for age-specific effects of chromosomal regions.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Atwood LD, Heard-Costa NL, Cupples LA, Jaquish CE, Wilson PW, D'Agostino RB: Genomewide Linkage Analysis of Body Mass Index across 28 Years of the Framingham Heart Study. American Journal of Human Genetics. 2002, 71 (5): 1044-1050. 10.1086/343822. 2. Perusse L, Rankinen T, Zuberi A, Chagnon YC, Weisnagel SJ, Argyropoulos G, Walts B, Snyder EE, Bouchard C: The human obesity gene map: the 2004 update. Obes Res. 2005, 13 (3): 381-490. 3. Stone S, Abkevich V, Hunt SC, Gutin A, Russell DL, Neff CD, Riley R, Frech GC, Hensel CH, Jammulapati S, Potter J, Sexton D, Tran T, Gibbs D, Iliev D, Gress R, Bloomquist B, Amatruda J, Rae PM, Adams TD, Skolnick MH, Shattuck D: A Major Predisposition Locus for Severe Obesity, at 4p15-p14. Am J Hum Genet. 2002, 70 (6): 1459-1468. 10.1086/340670. 4. Lewis CE, North KE, Arnett D, Borecki IB, Coon H, Ellison RC, Hunt SC, Oberman A, Rich SS, Province MA, Miller MB: Sex-specific findings from a genome-wide linkage analysis of human fatness in non-Hispanic whites and African Americans: The HyperGEN Study. Int J Obes Relat Metab Disord. 2005 5. Allison DB, Neale MC, Zannolli R, Schork NJ, Amos CI, Blangero J: Testing the robustness of the likelihood-ratio test in a variance- component quantitative-trait loci-mapping procedure. Am J Hum Genet. 1999, 65 (2): 531-544. 10.1086/302487.
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