PO.BCS01.16 · 生物信息与计算

MPACT-DPD: An interpretable machine learning classifier for predicting the functional impact of DPYD missense variants

海报缩略图:MPACT-DPD: An interpretable machine learning classifier for predicting the functional impact of DPYD missense variants
编号 2712 展板 5 时间 4/20 02:00–05:00 区域 Section 2 主讲 Jiayue Jiang, BA;MS
分会场 Integration of Clinical and Research Data
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作者与单位

Lulu Jiang1, Ryan Jonathan Swartz2, Lauryn Allyn Hahn2, Brianna Bembenek3, Hannah Marie Krause4, Kelly Bouchonville4, Steven M. Offer4

1Informatics, University of Iowa, Iowa City, IA,2Carver College of Medicine, University of Iowa, Iowa City, IA,3Mayo Clinic, Rochester, MN,4University of Iowa Holden Comprehensive Cancer Center, Iowa City, IA

摘要 Abstract

5-Fluorouracil (5-FU) is a widely prescribed chemotherapy for colorectal, breast, gastric, and head and neck cancers. The drug inhibits thymidylate synthase, blocking DNA synthesis and causing cytotoxic stress that halts tumor growth. However, patients carrying deleterious variants in DPYD , the gene encoding the rate-limiting enzyme in 5-FU metabolism (dihydropyrimidine dehydrogenase, DPD), can experience fatal toxicity due to impaired drug clearance and accumulation of 5-FU metabolites. Current pharmacogenetic screening guidelines in the U.S. recommend testing for few of the >2,000 nonsynonymous variants that have been reported for DPYD , leaving patients with rare, uncharacterized mutations at risk. To interpret expanded testing, however, a means to classify DPYD variants of unknown significance is needed. To address this, we developed MPACT-DPD, a random-forest-based classifier that accurately predicts the functional impact of DPYD missense variants. Our model was trained on in-vitro activity of 156 variants and leveraged a feature set of biochemical, evolutionary, and AlphaFold3-derived structural features. We optimized hyperparameters using ten-fold stratified cross-validation and evaluated model performance with Matthews correlation coefficient (MCC) to account for moderate class imbalance (7:3 neutral to deleterious). It achieved exceptional performance, with a Matthews correlation coeffient (MCC) of 0.906 and an accuracy of 95.1% on an independent validation set (n=43). Furthermore, a SHAP (SHapley Additive exPlanations)-based interpretability analysis revealed cofactor proximity and residue conservation as the key drivers of predictions. MPACT-DPD showed superior performance at variant classification against other tools, including a DPYD gene-specific variant classifier, and has the potential to expand pre-treatment genetic screening to improve the safety of personalized 5-FU-based chemotherapy.
利益披露 Disclosure
L. Jiang, None.. B. Bembenek, None.. K. Bouchonville, None.. S. M. Offer, None.

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