Evidence map›Paper›PMID 41054307›Full record

ArticleRenal failure2025

Optimizing α-galactosidase A enzyme cutoff for Fabry disease screening in chronic kidney disease patients: a single-center reassessment of diagnostic yield and cost-effectiveness.

Shang-Feng Tsai, Ming-Ju Wu, Hsien-Hsu Hsieh, Cheng-Hsu Chen

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Article in Renal failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Shang-Feng TsaiDivision of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Ming-Ju WuDivision of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Hsien-Hsu HsiehDepartment of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Cheng-Hsu ChenDivision of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease has been increasingly recognized in patients with chronic kidney disease (CKD). While dried blood spot (DBS) testing for α-galactosidase A (α-Gal A) activity is a common screening method, the optimal cutoff value for enzyme activity in this population remains uncertain. We retrospectively analyzed data from a Fabry disease screening program conducted between October 1, 2018, and September 31, 2023, at Taichung Veterans General Hospital. Male patients with CKD or ESKD underwent DBS α-Gal A enzyme activity testing. Patients with enzyme activity <2.0 μmol/L/hr were referred for confirmatory genetic testing. We assessed the diagnostic yield, baseline characteristics of true positive, false positive, and true negative cases, and performed receiver operating characteristic (ROC) analysis to identify the optimal diagnostic threshold. Among 1,654 screened patients, 35 had enzyme activity <2.0 μmol/L/hr, of whom 6 (0.36%) were genetically confirmed as having Fabry disease. Broadening the screening threshold from 1.2 to 2.0 μmol/L/hr enabled the identification of two additional cases. ROC analysis identified an optimal cutoff value of 1.96 μmol/L/hr (AUROC 0.996, 95%CI: 0.991-1.000), yielding a sensitivity of 98.3% (95CI%: 0.9769-0.9891) and specificity of 100% (95%CI:1-1). Patients with false-positive results had significantly lower leukocyte counts than true-positive cases. The incremental cost to detect two additional Fabry patients was $8,010 USD, representing acceptable cost-effectiveness under Taiwan's healthcare framework. Expanding α-Gal A enzyme activity cutoff value from 1.2 to 2.0 μmol/L/hr improved the diagnostic performance of Fabry disease screening in CKD patients and proved to be cost-effective.

Indexed as

alpha-GalactosidaseFabry DiseaseMass ScreeningRenal Insufficiency, ChronicAdultAgedCost-Benefit AnalysisDried Blood Spot TestingHumansMaleMiddle AgedRetrospective StudiesROC CurveSensitivity and SpecificityTaiwanalpha-Galactosidasealpha galactosidase (α-Gal) activitychronic kidney diseasecutoff valueFabry diseasehemodialysisperitoneal dialysis

Identifiers

PMID41054307
PMCPMC12507110

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.