PMID- 30935434 OWN - NLM STAT- MEDLINE DCOM- 20200512 LR - 20200512 IS - 1475-2662 (Electronic) IS - 0007-1145 (Linking) VI - 122 IP - 1 DP - 2019 Jul 14 TI - Prediction model for the efficacy of folic acid therapy on hyperhomocysteinaemia based on genetic risk score methods. PG - 39-46 LID - 10.1017/S0007114519000783 [doi] AB - No risk assessment tools for the efficacy of folic acid treatment for hyperhomocysteinaemia (HHcy) have been developed. We aimed to use two common genetic risk score (GRS) methods to construct prediction models for the efficacy of folic acid therapy on HHcy, and the best gene-environment prediction model was screened out. A prospective cohort study enrolling 638 HHcy patients was performed. We used a logistic regression model to estimate the associations of two GRS methods with the efficacy. Performances were compared using area under the receiver operating characteristic curve (AUC). The simple count genetic risk score (SC-GRS) and weighted genetic risk score (wGRS) were found to be independently associated with the efficacy of folic acid treatment for HHcy. Using the SC-GRS, per risk allele increased with a 1.46-fold increased failure risk (P < 0.001) after adjustment for traditional risk factors, including age, sex, BMI, smoking, alcohol consumption, history of diabetes, history of hypertension, history of hyperlipidaemia, history of stroke and history of CHD. When used the wGRS, the association was strengthened (OR = 2.08, P < 0.001). Addition of the SC-GRS and wGRS to the traditional risk model significantly improved the predictive ability by AUC (0.859). A precise gene-environment predictive model with good performance was developed for predicting the treatment failure rate of folic acid therapy for HHcy. FAU - Du, Binghui AU - Du B AD - Department of Epidemiology, School of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China. FAU - Zhang, Chengda AU - Zhang C AD - Department of Internal Medicine, Beaumont Hospital, Royal Oak, MI, USA. FAU - Yue, Limin AU - Yue L AD - Department of Epidemiology, School of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China. FAU - Ren, Bingnan AU - Ren B AD - Department of Epidemiology, School of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China. FAU - Zhao, Qinglin AU - Zhao Q AD - Department of Epidemiology, School of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China. FAU - Li, Dankang AU - Li D AD - Department of Epidemiology, School of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China. FAU - He, Yuanhong AU - He Y AD - The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China. FAU - Zhang, Weidong AU - Zhang W AD - Department of Epidemiology, School of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20190628 PL - England TA - Br J Nutr JT - The British journal of nutrition JID - 0372547 RN - 935E97BOY8 (Folic Acid) SB - IM MH - Adult MH - Aged MH - Female MH - Folic Acid/administration & dosage/*therapeutic use MH - Genetic Predisposition to Disease MH - Humans MH - Hyperhomocysteinemia/*drug therapy/*genetics MH - Male MH - Middle Aged MH - Models, Biological MH - Polymorphism, Single Nucleotide OTO - NOTNLM OT - Efficacy OT - Folic acid OT - Genetic risk score OT - Hyperhomocysteinaemia OT - Risk prediction EDAT- 2019/04/03 06:00 MHDA- 2020/05/13 06:00 CRDT- 2019/04/03 06:00 PHST- 2019/04/03 06:00 [pubmed] PHST- 2020/05/13 06:00 [medline] PHST- 2019/04/03 06:00 [entrez] AID - S0007114519000783 [pii] AID - 10.1017/S0007114519000783 [doi] PST - ppublish SO - Br J Nutr. 2019 Jul 14;122(1):39-46. doi: 10.1017/S0007114519000783. Epub 2019 Jun 28.