Prediction of Adulthood Obesity Using Genetic and Childhood Clinical Risk Factors in the Cardiovascular Risk in Young Finns Study. (June 2017)
- Record Type:
- Journal Article
- Title:
- Prediction of Adulthood Obesity Using Genetic and Childhood Clinical Risk Factors in the Cardiovascular Risk in Young Finns Study. (June 2017)
- Main Title:
- Prediction of Adulthood Obesity Using Genetic and Childhood Clinical Risk Factors in the Cardiovascular Risk in Young Finns Study
- Authors:
- Seyednasrollah, Fatemeh
Mäkelä, Johanna
Pitkänen, Niina
Juonala, Markus
Hutri-Kähönen, Nina
Lehtimäki, Terho
Viikari, Jorma
Kelly, Tanika
Li, Changwei
Bazzano, Lydia
Elo, Laura L.
Raitakari, Olli T. - Abstract:
- Abstract : Background—: Obesity is a known risk factor for cardiovascular disease. Early prediction of obesity is essential for prevention. The aim of this study is to assess the use of childhood clinical factors and the genetic risk factors in predicting adulthood obesity using machine learning methods. Methods and Results—: A total of 2262 participants from the Cardiovascular Risk in YFS (Young Finns Study) were followed up from childhood (age 3–18 years) to adulthood for 31 years. The data were divided into training (n=1625) and validation (n=637) set. The effect of known genetic risk factors (97 single-nucleotide polymorphisms) was investigated as a weighted genetic risk score of all 97 single-nucleotide polymorphisms (WGRS97) or a subset of 19 most significant single-nucleotide polymorphisms (WGRS19) using boosting machine learning technique. WGRS97 and WGRS19 were validated using external data (n=369) from BHS (Bogalusa Heart Study). WGRS19 improved the accuracy of predicting adulthood obesity in training (area under the curve [AUC=0.787 versus AUC=0.744, P <0.0001) and validation data (AUC=0.769 versus AUC=0.747, P =0.026). WGRS97 improved the accuracy in training (AUC=0.782 versus AUC=0.744, P <0.0001) but not in validation data (AUC=0.749 versus AUC=0.747, P =0.785). Higher WGRS19 associated with higher body mass index at 9 years and WGRS97 at 6 years. Replication in BHS confirmed our findings that WGRS19 and WGRS97 are associated with body mass index. Conclusions—:Abstract : Background—: Obesity is a known risk factor for cardiovascular disease. Early prediction of obesity is essential for prevention. The aim of this study is to assess the use of childhood clinical factors and the genetic risk factors in predicting adulthood obesity using machine learning methods. Methods and Results—: A total of 2262 participants from the Cardiovascular Risk in YFS (Young Finns Study) were followed up from childhood (age 3–18 years) to adulthood for 31 years. The data were divided into training (n=1625) and validation (n=637) set. The effect of known genetic risk factors (97 single-nucleotide polymorphisms) was investigated as a weighted genetic risk score of all 97 single-nucleotide polymorphisms (WGRS97) or a subset of 19 most significant single-nucleotide polymorphisms (WGRS19) using boosting machine learning technique. WGRS97 and WGRS19 were validated using external data (n=369) from BHS (Bogalusa Heart Study). WGRS19 improved the accuracy of predicting adulthood obesity in training (area under the curve [AUC=0.787 versus AUC=0.744, P <0.0001) and validation data (AUC=0.769 versus AUC=0.747, P =0.026). WGRS97 improved the accuracy in training (AUC=0.782 versus AUC=0.744, P <0.0001) but not in validation data (AUC=0.749 versus AUC=0.747, P =0.785). Higher WGRS19 associated with higher body mass index at 9 years and WGRS97 at 6 years. Replication in BHS confirmed our findings that WGRS19 and WGRS97 are associated with body mass index. Conclusions—: WGRS19 improves prediction of adulthood obesity. Predictive accuracy is highest among young children (3–6 years), whereas among older children (9–18 years) the risk can be identified using childhood clinical factors. The model is helpful in screening children with high risk of developing obesity. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Circulation. Volume 10:Number 3(2017)
- Journal:
- Circulation
- Issue:
- Volume 10:Number 3(2017)
- Issue Display:
- Volume 10, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 10
- Issue:
- 3
- Issue Sort Value:
- 2017-0010-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-06
- Subjects:
- genetics -- machine learning -- obesity -- risk factor -- single-nucleotide polymorphism genetics -- statistics
Arrhythmia -- Periodicals
Heart -- Electric properties -- Periodicals
616.1042 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=01337497-000000000-00000 ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCGENETICS.116.001554 ↗
- Languages:
- English
- ISSNs:
- 1942-325X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.262520
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4588.xml