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Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland
BACKGROUND: The salivary α-amylase locus (AMY1) is located in a highly polymorphic multi allelic copy number variable chromosomal region. A recent report identified an association between AMY1 copy numbers and BMI in common obesity. The present study investigated the relationship between AMY1 copy n...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489572/ https://www.ncbi.nlm.nih.gov/pubmed/26132294 http://dx.doi.org/10.1371/journal.pone.0131883 |
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author | Viljakainen, Heli Andersson-Assarsson, Johanna C Armenio, Miriam Pekkinen, Minna Pettersson, Maria Valta, Helena Lipsanen-Nyman, Marita Mäkitie, Outi Lindstrand, Anna |
author_facet | Viljakainen, Heli Andersson-Assarsson, Johanna C Armenio, Miriam Pekkinen, Minna Pettersson, Maria Valta, Helena Lipsanen-Nyman, Marita Mäkitie, Outi Lindstrand, Anna |
author_sort | Viljakainen, Heli |
collection | PubMed |
description | BACKGROUND: The salivary α-amylase locus (AMY1) is located in a highly polymorphic multi allelic copy number variable chromosomal region. A recent report identified an association between AMY1 copy numbers and BMI in common obesity. The present study investigated the relationship between AMY1 copy number, BMI and serum amylase in childhood-onset obesity. PATIENTS: Sixty-one subjects with a history of childhood-onset obesity (mean age 19.1 years, 54% males) and 71 matched controls (19.8 yrs, 45% males) were included. All anthropometric measures were greater in the obese; their mean BMI was 40 kg/m(2) (range 25-62 kg/m(2)) compared with 23 kg/m(2) in the controls (15-32 kg/m(2)). RESULTS: Mean AMY1 copy numbers did not differ between the obese and control subjects, but gender differences were observed; obese men showed the highest and obese women the lowest number of AMY1 copies (p=0.045). Further, only in affected females, AMY1 copy number correlated significantly with whole body fat percent (r=-0.512, p=0.013) and BMI (r=-0.416, p=0.025). Finally, a clear linear association between AMY1 copy number and serum salivary amylase was observed in all subgroups but again differences existed between obese males and females. CONCLUSIONS: In conclusion, our findings suggest that AMY1 copy number differences play a role in childhood-onset obesity but the effect differs between males and females. Further studies in larger cohorts are needed to confirm these observations. |
format | Online Article Text |
id | pubmed-4489572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44895722015-07-14 Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland Viljakainen, Heli Andersson-Assarsson, Johanna C Armenio, Miriam Pekkinen, Minna Pettersson, Maria Valta, Helena Lipsanen-Nyman, Marita Mäkitie, Outi Lindstrand, Anna PLoS One Research Article BACKGROUND: The salivary α-amylase locus (AMY1) is located in a highly polymorphic multi allelic copy number variable chromosomal region. A recent report identified an association between AMY1 copy numbers and BMI in common obesity. The present study investigated the relationship between AMY1 copy number, BMI and serum amylase in childhood-onset obesity. PATIENTS: Sixty-one subjects with a history of childhood-onset obesity (mean age 19.1 years, 54% males) and 71 matched controls (19.8 yrs, 45% males) were included. All anthropometric measures were greater in the obese; their mean BMI was 40 kg/m(2) (range 25-62 kg/m(2)) compared with 23 kg/m(2) in the controls (15-32 kg/m(2)). RESULTS: Mean AMY1 copy numbers did not differ between the obese and control subjects, but gender differences were observed; obese men showed the highest and obese women the lowest number of AMY1 copies (p=0.045). Further, only in affected females, AMY1 copy number correlated significantly with whole body fat percent (r=-0.512, p=0.013) and BMI (r=-0.416, p=0.025). Finally, a clear linear association between AMY1 copy number and serum salivary amylase was observed in all subgroups but again differences existed between obese males and females. CONCLUSIONS: In conclusion, our findings suggest that AMY1 copy number differences play a role in childhood-onset obesity but the effect differs between males and females. Further studies in larger cohorts are needed to confirm these observations. Public Library of Science 2015-07-01 /pmc/articles/PMC4489572/ /pubmed/26132294 http://dx.doi.org/10.1371/journal.pone.0131883 Text en © 2015 Viljakainen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Viljakainen, Heli Andersson-Assarsson, Johanna C Armenio, Miriam Pekkinen, Minna Pettersson, Maria Valta, Helena Lipsanen-Nyman, Marita Mäkitie, Outi Lindstrand, Anna Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland |
title | Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland |
title_full | Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland |
title_fullStr | Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland |
title_full_unstemmed | Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland |
title_short | Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland |
title_sort | low copy number of the amy1 locus is associated with early-onset female obesity in finland |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489572/ https://www.ncbi.nlm.nih.gov/pubmed/26132294 http://dx.doi.org/10.1371/journal.pone.0131883 |
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