Electronic health records-based algorithms to screen for U.S. Centers for Disease Control and Prevention tier 1 genetic diseases: a scoping review

William R Harris & Jason L Vassy et al.

Abstract

Objective

Missed diagnosis of genetic conditions is a persistent challenge in clinical care, particularly for familial hypercholesterolemia (FH), hereditary breast and ovarian cancer (HBOC), and Lynch syndrome—conditions designated by the U.S. Centers for Disease Control and Prevention (CDC) as Tier 1 genomic applications. This scoping review summarizes evidence on the use of electronic health record (EHR)-based algorithms to identify individuals with these conditions.

Materials and Methods

We conducted a scoping review using the JBI Manual for Evidence Synthesis and reported results according to PRISMA-ScR guidelines. We searched Ovid MEDLINE, Embase, and Web of Science through October 2024 for studies evaluating EHR-based algorithms to identify individuals with FH, HBOC, or Lynch syndrome. Eligible studies addressed (1) performance of algorithms in detecting clinically or genetically confirmed cases or (2) outcomes from the implementation of algorithms in unselected populations with follow-up to identify new diagnoses.

Results

Of 598 articles screened, 22 met inclusion criteria. Most studies (20/22) focused on FH. Fourteen FH studies assessed algorithm performance, and 7 reported prospective implementation. FH algorithm performance varied widely (AUROC range 0.78-0.95), with machine learning models outperforming rule-based approaches. Implementation studies reported positive predictive values ranging from 11% to 67%. Only two studies addressed HBOC or Lynch syndrome, both using rules-based algorithms with limited sensitivity.

Discussion

Machine learning models consistently outperform rules-based algorithms relying on clinical criteria, but limited evidence exists for HBOC and Lynch syndrome.

Conclusions

Early identification of CDC Tier 1 genetic conditions through EHR-based screening algorithms holds promise but will require both technical and implementation advances to realize improved patient care and outcomes.

Funding
Mechanisms of NAT2 Regulation of Insulin Resistance and Mitochondrial DysfunctionBeyond GWAS of insulin resistance: An integrated approach to translate genetic association to functionMolecular Mechanisms of Insulin Resistance Associated LociBuilding a shared decision making implementation strategy for the emerging paradigm of precision cancer screeningThe VA Genomics Learning Health System: Implementing genomic medicine across diverse veteran communitiesMolecular Mechanisms of Insulin Resistance Associated LociThe Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS): A pragmatic trial of precision prostate cancer screeningDiabetes Genomics and Analysis CoreThe Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS): A pragmatic trial of precision prostate cancer screeningPragmatic randomized trial of polygenic risk scoring for common diseases in primary careDiabetes Genomics and Analysis CoreBuilding a shared decision making implementation strategy for the emerging paradigm of precision cancer screeningCharacterization of novel insulin resistance genes by gene editing, high-throughput phenotyping and in vivo studiesBuilding a shared decision making implementation strategy for the emerging paradigm of precision cancer screeningThe Prostate Cancer, Genetic Risk, and Equitable Screening Study (ProGRESS): A pragmatic trial of precision prostate cancer screening

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R01 DK106236

NIH HHS

R01 DK107437

VA

I01 HX003627

NHGRI NIH HHS

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NIH HHS

R01 DK137889

CSRD VA

I01 CX002635

NIDDK NIH HHS

R01 DK116750

NIDDK NIH HHS

P30 DK116074

VA

I01 CX002635

NIH HHS

R01 DK106236

NIH HHS

R35 HG010706

NIH HHS

U01 HG013781

NIH HHS

P30DK116074

HSRD VA

I01 HX003627

NIDDK NIH HHS

R01 DK120565

NIDDK NIH HHS

R01 DK107437

NHGRI NIH HHS

R35 HG010706

NIDDK NIH HHS

R01 DK137889

NIH HHS

R01 DK120565

National Institutes of Health

R35 HG010706

National Institutes of Health

U01 HG013781

Department of Veterans Affairs

I01 HX003627

Department of Veterans Affairs

I01 CX002635

NIH

R01 DK116750

NIH

R01 DK120565

NIH

R01 DK106236

NIH

R01 DK107437

NIH

R01 DK137889

NIH

P30DK116074