Mosaic Loss of Chromosome Y Is Associated With Functional Outcome After Ischemic Stroke

Author:

Dorvall Malin1ORCID,Pedersen Annie12ORCID,Dumanski Jan P.34ORCID,Söderholm Martin56ORCID,Lindgren Arne G.56ORCID,Stanne Tara M.1ORCID,Jern Christina12ORCID

Affiliation:

1. Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Sweden (M.D., A.P., T.M.S., C.J.).

2. Department of Clinical Genetics and Genomics, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden (A.P., C.J.).

3. Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Sweden (J.P.D.).

4. 3P-Medicine Laboratory, Medical University of Gdańsk, Poland (J.P.D.).

5. Department of Clinical Sciences Lund, Neurology, Lund University, Sweden (M.S., A.G.L.).

6. Department of Neurology, Skåne University Hospital, Lund and Malmö, Sweden (M.S., A.G.L.).

Abstract

BACKGROUND: Mosaic loss of chromosome Y (LOY) is associated with cardiovascular and neurodegenerative diseases in men, and genetic predisposition to LOY is associated with poor poststroke outcome. We, therefore, tested the hypothesis that LOY itself is associated with functional outcome after ischemic stroke. METHODS: The study comprised male patients with ischemic stroke from the cohort studies SAHLSIS2 (Sahlgrenska Academy Study on Ischemic Stroke Phase 2; n=588) and LSR (Lund Stroke Register; n=735). We used binary logistic regression to analyze associations between LOY, determined by DNA microarray intensity data, and poor 3-month functional outcome (modified Rankin Scale score, >2) in each cohort separately and combined. Patients who received recanalization therapy were excluded from sensitivity analyses. RESULTS: LOY was associated with about 2.5-fold increased risk of poor outcome in univariable analyses ( P <0.001). This association withstood separate adjustment for stroke severity and diabetes in both cohorts but not age. In sensitivity analyses restricted to the nonrecanalization group (n=987 in the combined cohort), the association was significant also after separate adjustment for age (odds ratio, 1.6 [95% CI, 1.1–2.4]) and when additionally adjusting for stroke severity and diabetes (odds ratio, 1.6 [95% CI, 1.1–2.5]). CONCLUSIONS: We observed an association between LOY and poor outcome after ischemic stroke in patients not receiving recanalization therapy. Future studies on LOY and other somatic genetic alterations in larger stroke cohorts are warranted.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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