Cargando…

Prediction model for knee osteoarthritis based on genetic and clinical information

INTRODUCTION: Osteoarthritis (OA) is the most common bone and joint disease influenced by genetic and environmental factors. Recent association studies have uncovered the genetic factors behind OA, its susceptibility genes, which would enable us to predict disease occurrence based on genotype inform...

Descripción completa

Detalles Bibliográficos
Autores principales: Takahashi, Hiroshi, Nakajima, Masahiro, Ozaki, Kouichi, Tanaka, Toshihiro, Kamatani, Naoyuki, Ikegawa, Shiro
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991022/
https://www.ncbi.nlm.nih.gov/pubmed/20939878
http://dx.doi.org/10.1186/ar3157
_version_ 1782192545365753856
author Takahashi, Hiroshi
Nakajima, Masahiro
Ozaki, Kouichi
Tanaka, Toshihiro
Kamatani, Naoyuki
Ikegawa, Shiro
author_facet Takahashi, Hiroshi
Nakajima, Masahiro
Ozaki, Kouichi
Tanaka, Toshihiro
Kamatani, Naoyuki
Ikegawa, Shiro
author_sort Takahashi, Hiroshi
collection PubMed
description INTRODUCTION: Osteoarthritis (OA) is the most common bone and joint disease influenced by genetic and environmental factors. Recent association studies have uncovered the genetic factors behind OA, its susceptibility genes, which would enable us to predict disease occurrence based on genotype information. However, most previous studies have evaluated the effects of only a single susceptibility gene, and hence prediction based on such information is not as reliable. Here, we constructed OA-prediction models based on genotype information from a case-control association study and tested their predictability. METHODS: We genotyped risk alleles of the three susceptibility genes, asporin (ASPN), growth differentiation factor 5 (GDF5), and double von Willebrand factor A domains (DVWA) for a total of 2,158 Japanese subjects (933 OA and 1,225 controls) and statistically analyzed their effects. After that, we constructed prediction models by using the logistic regression analysis. RESULTS: When the effects of each allele were assumed to be the same and multiplicative, each additional risk allele increased the odds ratio (OR) by a factor of 1.23 (95% confidence interval (CI), 1.12 to 1.34). Individuals with five or six risk alleles showed significantly higher susceptibility when compared with those with zero or one, with an OR of 2.67 (95% CI, 1.46 to 4.87; P = 0.0020). Statistical evaluation of the prediction power of models showed that a model using only genotyping data had poor predictability. We obtained a model with good predictability by incorporating clinical data, which was further improved by rigorous age adjustment. CONCLUSIONS: Our results showed that consideration of adjusted clinical information, as well as increases in the number of risk alleles to be integrated, is critical for OA prediction by using data from case-control studies. To the authors' knowledge, this is the first report of the OA-prediction model combining both genetic and clinical information.
format Text
id pubmed-2991022
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-29910222010-12-13 Prediction model for knee osteoarthritis based on genetic and clinical information Takahashi, Hiroshi Nakajima, Masahiro Ozaki, Kouichi Tanaka, Toshihiro Kamatani, Naoyuki Ikegawa, Shiro Arthritis Res Ther Research Article INTRODUCTION: Osteoarthritis (OA) is the most common bone and joint disease influenced by genetic and environmental factors. Recent association studies have uncovered the genetic factors behind OA, its susceptibility genes, which would enable us to predict disease occurrence based on genotype information. However, most previous studies have evaluated the effects of only a single susceptibility gene, and hence prediction based on such information is not as reliable. Here, we constructed OA-prediction models based on genotype information from a case-control association study and tested their predictability. METHODS: We genotyped risk alleles of the three susceptibility genes, asporin (ASPN), growth differentiation factor 5 (GDF5), and double von Willebrand factor A domains (DVWA) for a total of 2,158 Japanese subjects (933 OA and 1,225 controls) and statistically analyzed their effects. After that, we constructed prediction models by using the logistic regression analysis. RESULTS: When the effects of each allele were assumed to be the same and multiplicative, each additional risk allele increased the odds ratio (OR) by a factor of 1.23 (95% confidence interval (CI), 1.12 to 1.34). Individuals with five or six risk alleles showed significantly higher susceptibility when compared with those with zero or one, with an OR of 2.67 (95% CI, 1.46 to 4.87; P = 0.0020). Statistical evaluation of the prediction power of models showed that a model using only genotyping data had poor predictability. We obtained a model with good predictability by incorporating clinical data, which was further improved by rigorous age adjustment. CONCLUSIONS: Our results showed that consideration of adjusted clinical information, as well as increases in the number of risk alleles to be integrated, is critical for OA prediction by using data from case-control studies. To the authors' knowledge, this is the first report of the OA-prediction model combining both genetic and clinical information. BioMed Central 2010 2010-10-12 /pmc/articles/PMC2991022/ /pubmed/20939878 http://dx.doi.org/10.1186/ar3157 Text en Copyright ©2010 Takahashi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Takahashi, Hiroshi
Nakajima, Masahiro
Ozaki, Kouichi
Tanaka, Toshihiro
Kamatani, Naoyuki
Ikegawa, Shiro
Prediction model for knee osteoarthritis based on genetic and clinical information
title Prediction model for knee osteoarthritis based on genetic and clinical information
title_full Prediction model for knee osteoarthritis based on genetic and clinical information
title_fullStr Prediction model for knee osteoarthritis based on genetic and clinical information
title_full_unstemmed Prediction model for knee osteoarthritis based on genetic and clinical information
title_short Prediction model for knee osteoarthritis based on genetic and clinical information
title_sort prediction model for knee osteoarthritis based on genetic and clinical information
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991022/
https://www.ncbi.nlm.nih.gov/pubmed/20939878
http://dx.doi.org/10.1186/ar3157
work_keys_str_mv AT takahashihiroshi predictionmodelforkneeosteoarthritisbasedongeneticandclinicalinformation
AT nakajimamasahiro predictionmodelforkneeosteoarthritisbasedongeneticandclinicalinformation
AT ozakikouichi predictionmodelforkneeosteoarthritisbasedongeneticandclinicalinformation
AT tanakatoshihiro predictionmodelforkneeosteoarthritisbasedongeneticandclinicalinformation
AT kamataninaoyuki predictionmodelforkneeosteoarthritisbasedongeneticandclinicalinformation
AT ikegawashiro predictionmodelforkneeosteoarthritisbasedongeneticandclinicalinformation