Publication:
Cascade counselling and testing. Recommendations of the European Society of Human Genetics

dc.contributor.coauthorde Wert, Guido
dc.contributor.coauthorvan El, Carla G.
dc.contributor.coauthorClarke, Angus
dc.contributor.coauthorCordier, Christophe
dc.contributor.coauthorFellmann, Florence
dc.contributor.coauthorGenuardi, Maurizio
dc.contributor.coauthorHentze, Sabine
dc.contributor.coauthorMacek, Milan
dc.contributor.coauthorMacleod, Rhona
dc.contributor.coauthorMelegh, Bela
dc.contributor.coauthorMendes, Alvaro
dc.contributor.coauthorRial-Sebbag, Emmanuelle
dc.contributor.coauthorStefansdottir, Vigdis
dc.contributor.coauthorTranebjaerg, Lisbeth
dc.contributor.coauthorUlph, Fiona
dc.contributor.coauthorForzano, Francesca
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-01-16T08:45:42Z
dc.date.available2026-01-16
dc.date.issued2025
dc.description.abstractCascade testing (CT) is an effective instrument for identifying an index patient's relatives at high risk of a heritable condition enabling informed decision-making on preventive interventions and reproductive choice. However, CT remains underutilised and faces barriers. Discussions are ongoing on how to optimise informing family members and testing uptake in a responsible manner. The European Society of Human Genetics (ESHG) contributes to this debate and provides recommendations based on an ethical analysis of when CT is justified, or may be less compelling, considering proportionality and the judicious use of finite resources. ESHG underscores the strong consensus regarding the 'moral architecture' of CT in cases of a high risk of serious, avoidable harm. In such cases, a more active approach towards CT is suggested, including a more directive approach in counselling, more active support for the proband, direct contacting, and balancing confidentiality when this is necessary to avoid a high risk of serious harm, taking account of national regulations and jurisdictions. In contrast, more caution is advised in more complex cases where the balance of benefits and harms of CT is less clear, such as when penetrance is low, and actionability or medical treatment is limited. This more cautious approach does not call for directivity, direct contact or the relaxing of medical confidentiality. The focus, then, shifts to cascade counselling, rather than cascade testing. In some cases, CT may not be proportional or appropriate given the balance between benefits and harms, also in view of available resources.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessHybrid OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipEuropean Society of Human Genetics
dc.identifier.doi10.1038/s41431-025-01945-3
dc.identifier.eissn1476-5438
dc.identifier.embargoNo
dc.identifier.issn1018-4813
dc.identifier.pubmed41392321
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-105024796850
dc.identifier.urihttps://doi.org/10.1038/s41431-025-01945-3
dc.identifier.urihttps://hdl.handle.net/20.500.14288/32039
dc.identifier.wos001637677000001
dc.keywordsFamilial hypercholesterolemia
dc.keywordsSickle-cell
dc.keywordsHuntingtons-disease
dc.keywordsHereditary conditions
dc.keywordsRisk information
dc.keywordsDecision-making
dc.keywordsLynch syndrome
dc.keywordsCommunication
dc.keywordsParents
dc.keywordsCancer
dc.language.isoeng
dc.publisherSpringer
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofEuropean Journal of Human Genetics
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectBiochemistry and molecular biology
dc.subjectGenetics and heredity
dc.titleCascade counselling and testing. Recommendations of the European Society of Human Genetics
dc.typeJournal Article
dspace.entity.typePublication
person.familyNameKayserili
person.givenNameHülya
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