Literature DB >> 25069673

Likelihood ratio-based integrated personal risk assessment of type 2 diabetes.

Noriko Sato1, Nay Chi Htun, Makoto Daimon, Gen Tamiya, Takeo Kato, Isao Kubota, Yoshiyuki Ueno, Hidetoshi Yamashita, Akira Fukao, Takamasa Kayama, Masaaki Muramatsu.   

Abstract

To facilitate personalized health care for multifactorial diseases, risks of genetic and clinical/environmental factors should be assessed together for each individual in an integrated fashion. This approach is possible with the likelihood ratio (LR)-based risk assessment system, as this system can incorporate manifold tests. We examined the usefulness of this system for assessing type 2 diabetes (T2D). Our system employed 29 genetic susceptibility variants, body mass index (BMI), and hypertension as risk factors whose LRs can be estimated from openly available T2D association data for the Japanese population. The pretest probability was set at a sex- and age-appropriate population average of diabetes prevalence. The classification performance of our LR-based risk assessment was compared to that of a non-invasive screening test for diabetes called TOPICS (with score based on age, sex, family history, smoking, BMI, and hypertension) using receiver operating characteristic analysis with a community cohort (n = 1263). The area under the receiver operating characteristic curve (AUC) for the LR-based assessment and TOPICS was 0.707 (95% CI 0.665-0.750) and 0.719 (0.675-0.762), respectively. These AUCs were much higher than that of a genetic risk score constructed using the same genetic susceptibility variants, 0.624 (0.574-0.674). The use of ethnically matched LRs is necessary for proper personal risk assessment. In conclusion, although LR-based integrated risk assessment for T2D still requires additional tests that evaluate other factors, such as risks involved in missing heritability, our results indicate the potential usability of LR-based assessment system and stress the importance of stratified epidemiological investigations in personalized medicine.

Entities:  

Mesh:

Year:  2014        PMID: 25069673     DOI: 10.1507/endocrj.ej14-0271

Source DB:  PubMed          Journal:  Endocr J        ISSN: 0918-8959            Impact factor:   2.349


  1 in total

1.  VaDE: a manually curated database of reproducible associations between various traits and human genomic polymorphisms.

Authors:  Yoko Nagai; Yasuko Takahashi; Tadashi Imanishi
Journal:  Nucleic Acids Res       Date:  2014-10-31       Impact factor: 19.160

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.