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Candidate Genes from an FDA-Approved Algorithm Fail to Predict Opioid Use Disorder Risk in Over 450,000 Veterans.
Davis, Christal N; Jinwala, Zeal; Hatoum, Alexander S; Toikumo, Sylvanus; Agrawal, Arpana; Rentsch, Christopher T; Edenberg, Howard J; Baurley, James W; Hartwell, Emily E; Crist, Richard C; Gray, Joshua C; Justice, Amy C; Gelernter, Joel; Kember, Rachel L; Kranzler, Henry R.
Affiliation
  • Davis CN; Mental Illness Research, Education and Clinical Center, Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
  • Jinwala Z; Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
  • Hatoum AS; Mental Illness Research, Education and Clinical Center, Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
  • Toikumo S; Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
  • Agrawal A; Department of Psychological and Brain Sciences, Washington University School of Medicine, St. Louis, MO, USA.
  • Rentsch CT; Mental Illness Research, Education and Clinical Center, Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
  • Edenberg HJ; Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
  • Baurley JW; Department of Psychiatry, Washington University, St. Louis, MO, USA.
  • Hartwell EE; Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA.
  • Crist RC; Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
  • Gray JC; Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
  • Justice AC; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Gelernter J; BioRealm LLC, Walnut, CA, USA.
  • Kember RL; Mental Illness Research, Education and Clinical Center, Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
  • Kranzler HR; Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
medRxiv ; 2024 May 16.
Article in En | MEDLINE | ID: mdl-38798430
ABSTRACT
Importance Recently, the Food and Drug Administration gave pre-marketing approval to algorithm based on its purported ability to identify genetic risk for opioid use disorder. However, the clinical utility of the candidate genes comprising the algorithm has not been independently demonstrated.

Objective:

To assess the utility of 15 variants in candidate genes from an algorithm intended to predict opioid use disorder risk.

Design:

This case-control study examined the association of 15 candidate genetic variants with risk of opioid use disorder using available electronic health record data from December 20, 1992 to September 30, 2022.

Setting:

Electronic health record data, including pharmacy records, from Million Veteran Program participants across the United States.

Participants:

Participants were opioid-exposed individuals enrolled in the Million Veteran Program (n = 452,664). Opioid use disorder cases were identified using International Classification of Disease diagnostic codes, and controls were individuals with no opioid use disorder diagnosis. Exposures Number of risk alleles present across 15 candidate genetic variants. Main Outcome and

Measures:

Predictive performance of 15 genetic variants for opioid use disorder risk assessed via logistic regression and machine learning models.

Results:

Opioid exposed individuals (n=33,669 cases) were on average 61.15 (SD = 13.37) years old, 90.46% male, and had varied genetic similarity to global reference panels. Collectively, the 15 candidate genetic variants accounted for 0.4% of variation in opioid use disorder risk. The accuracy of the ensemble machine learning model using the 15 genes as predictors was 52.8% (95% CI = 52.1 - 53.6%) in an independent testing sample. Conclusions and Relevance Candidate genes that comprise the approved algorithm do not meet reasonable standards of efficacy in predicting opioid use disorder risk. Given the algorithm's limited predictive accuracy, its use in clinical care would lead to high rates of false positive and negative findings. More clinically useful models are needed to identify individuals at risk of developing opioid use disorder.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MedRxiv Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MedRxiv Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States