Population Genomics for Familial Hypercholesterolemia: Return of Results, Cascade Testing, and Health System Readiness, Current Evidence and Gaps

Kamanzi Ntakirutimana G.

School of Natural and Applied Sciences Kampala International University Uganda

ABSTRACT

Familial hypercholesterolemia (FH) is a common inherited lipid disorder associated with markedly elevated cholesterol levels and a substantially increased risk of premature cardiovascular disease. Advances in population genomics, including biobank sequencing, newborn screening initiatives, and genotype-first approaches, have created new opportunities for early identification of individuals with pathogenic FH variants and for systematic cascade testing of at-risk relatives. This narrative review synthesizes current evidence on three critical domains shaping the implementation of population genomics for FH: return of genomic results, cascade testing processes, and health-system readiness. The literature indicates that returning genomic results can enhance early diagnosis and preventive treatment, yet practices vary widely regarding disclosure methods, patient engagement, and integration with cardiovascular risk assessment. Cascade testing remains the most effective and cost-efficient strategy for identifying affected relatives, but uptake is consistently low due to communication barriers, limited digital infrastructure, and insufficient clinical coordination. Ethical, legal, and social considerations, including informed consent, privacy, potential stigma, and equitable access to testing, further complicate implementation. Evidence on health-system readiness highlights important gaps in laboratory capacity, workforce training, interoperability of genomic and clinical data systems, reimbursement models, and long-term sustainability planning. Overall, population genomics offers substantial promise for improving FH detection and prevention of cardiovascular disease at scale. However, successful implementation will require standardized return-of-results frameworks, strengthened cascade-testing pathways, equity-focused policies, and coordinated health-system investments. Future research should prioritize longitudinal outcome studies, evaluation of digital and patient-centered communication tools, and cross-jurisdictional implementation frameworks to ensure that population genomic screening for FH translates into measurable public-health benefits.

Keywords: Familial hypercholesterolemia, Population genomics, Cascade testing, Return of genomic results, and Health system readiness

CITE AS: Kamanzi Ntakirutimana G. (2026). Population Genomics for Familial Hypercholesterolemia: Return of Results, Cascade Testing, and Health System Readiness, Current Evidence and Gaps. RESEARCH INVENTION JOURNAL OF PUBLIC HEALTH AND PHARMACY 5(1): 46-52. https://doi.org/10.59298/RIJPP/2026/514652