Lifelong cerebrovascular disease burden among CADASIL patients: analysis from a global health research network
Data reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited. We sought to evaluate the overt cerebrovascular disease burden among patients with CADASIL. Harmonized electronic medic...
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Published in | Frontiers in neurology Vol. 14; p. 1203985 |
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Abstract | Data reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited. We sought to evaluate the overt cerebrovascular disease burden among patients with CADASIL.
Harmonized electronic medical records were extracted from the TriNetX global health research network. CADASIL patients were identified using diagnostic codes and those with/without history of documented stroke sub-types (ischemic stroke [IS], intracerebral hemorrhage [ICH], subarachnoid hemorrhage [SAH] and transient ischemic attack [TIA]) were compared. Adjusted odds ratios (OR) and 95% confidence intervals (CI) of stroke incidence and mortality associated with sex were computed.
Between September 2018 and April 2020, 914 CADASIL patients were identified (median [IQR] age: 60 [50-69], 61.3% females); of whom 596 (65.2%) had documented cerebrovascular events (i.e., CADASIL-Stroke patients). Among CADASIL-Stroke patients, 89.4% experienced an IS, co-existing with TIAs in 27.7% and hemorrhagic strokes in 6.2%; initial stroke events occurred ≤65 years of age in 71% of patients. CADASIL-Stroke patients (vs. CADASIL-non-Stroke) had higher cardiovascular and neurological (migraines, cognitive impairment, epilepsy/seizures, mood disorders) burden. In age- and comorbidity-adjusted models, males had higher associated risk of stroke onset (OR: 1.37, CI: 1.01-1.86). Mortality risk was higher for males (OR: 2.72, CI: 1.53-4.84).
Early screening and targeted treatment strategies are warranted to help CADASIL patients with symptom management and risk mitigation. |
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AbstractList | Data reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited. We sought to evaluate the overt cerebrovascular disease burden among patients with CADASIL.
Harmonized electronic medical records were extracted from the TriNetX global health research network. CADASIL patients were identified using diagnostic codes and those with/without history of documented stroke sub-types (ischemic stroke [IS], intracerebral hemorrhage [ICH], subarachnoid hemorrhage [SAH] and transient ischemic attack [TIA]) were compared. Adjusted odds ratios (OR) and 95% confidence intervals (CI) of stroke incidence and mortality associated with sex were computed.
Between September 2018 and April 2020, 914 CADASIL patients were identified (median [IQR] age: 60 [50-69], 61.3% females); of whom 596 (65.2%) had documented cerebrovascular events (i.e., CADASIL-Stroke patients). Among CADASIL-Stroke patients, 89.4% experienced an IS, co-existing with TIAs in 27.7% and hemorrhagic strokes in 6.2%; initial stroke events occurred ≤65 years of age in 71% of patients. CADASIL-Stroke patients (vs. CADASIL-non-Stroke) had higher cardiovascular and neurological (migraines, cognitive impairment, epilepsy/seizures, mood disorders) burden. In age- and comorbidity-adjusted models, males had higher associated risk of stroke onset (OR: 1.37, CI: 1.01-1.86). Mortality risk was higher for males (OR: 2.72, CI: 1.53-4.84).
Early screening and targeted treatment strategies are warranted to help CADASIL patients with symptom management and risk mitigation. Data reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited. We sought to evaluate the overt cerebrovascular disease burden among patients with CADASIL.IntroductionData reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited. We sought to evaluate the overt cerebrovascular disease burden among patients with CADASIL.Harmonized electronic medical records were extracted from the TriNetX global health research network. CADASIL patients were identified using diagnostic codes and those with/without history of documented stroke sub-types (ischemic stroke [IS], intracerebral hemorrhage [ICH], subarachnoid hemorrhage [SAH] and transient ischemic attack [TIA]) were compared. Adjusted odds ratios (OR) and 95% confidence intervals (CI) of stroke incidence and mortality associated with sex were computed.MethodsHarmonized electronic medical records were extracted from the TriNetX global health research network. CADASIL patients were identified using diagnostic codes and those with/without history of documented stroke sub-types (ischemic stroke [IS], intracerebral hemorrhage [ICH], subarachnoid hemorrhage [SAH] and transient ischemic attack [TIA]) were compared. Adjusted odds ratios (OR) and 95% confidence intervals (CI) of stroke incidence and mortality associated with sex were computed.Between September 2018 and April 2020, 914 CADASIL patients were identified (median [IQR] age: 60 [50-69], 61.3% females); of whom 596 (65.2%) had documented cerebrovascular events (i.e., CADASIL-Stroke patients). Among CADASIL-Stroke patients, 89.4% experienced an IS, co-existing with TIAs in 27.7% and hemorrhagic strokes in 6.2%; initial stroke events occurred ≤65 years of age in 71% of patients. CADASIL-Stroke patients (vs. CADASIL-non-Stroke) had higher cardiovascular and neurological (migraines, cognitive impairment, epilepsy/seizures, mood disorders) burden. In age- and comorbidity-adjusted models, males had higher associated risk of stroke onset (OR: 1.37, CI: 1.01-1.86). Mortality risk was higher for males (OR: 2.72, CI: 1.53-4.84).ResultsBetween September 2018 and April 2020, 914 CADASIL patients were identified (median [IQR] age: 60 [50-69], 61.3% females); of whom 596 (65.2%) had documented cerebrovascular events (i.e., CADASIL-Stroke patients). Among CADASIL-Stroke patients, 89.4% experienced an IS, co-existing with TIAs in 27.7% and hemorrhagic strokes in 6.2%; initial stroke events occurred ≤65 years of age in 71% of patients. CADASIL-Stroke patients (vs. CADASIL-non-Stroke) had higher cardiovascular and neurological (migraines, cognitive impairment, epilepsy/seizures, mood disorders) burden. In age- and comorbidity-adjusted models, males had higher associated risk of stroke onset (OR: 1.37, CI: 1.01-1.86). Mortality risk was higher for males (OR: 2.72, CI: 1.53-4.84).Early screening and targeted treatment strategies are warranted to help CADASIL patients with symptom management and risk mitigation.DiscussionEarly screening and targeted treatment strategies are warranted to help CADASIL patients with symptom management and risk mitigation. IntroductionData reporting on patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) within the United States population is limited. We sought to evaluate the overt cerebrovascular disease burden among patients with CADASIL.MethodsHarmonized electronic medical records were extracted from the TriNetX global health research network. CADASIL patients were identified using diagnostic codes and those with/without history of documented stroke sub-types (ischemic stroke [IS], intracerebral hemorrhage [ICH], subarachnoid hemorrhage [SAH] and transient ischemic attack [TIA]) were compared. Adjusted odds ratios (OR) and 95% confidence intervals (CI) of stroke incidence and mortality associated with sex were computed.ResultsBetween September 2018 and April 2020, 914 CADASIL patients were identified (median [IQR] age: 60 [50–69], 61.3% females); of whom 596 (65.2%) had documented cerebrovascular events (i.e., CADASIL-Stroke patients). Among CADASIL-Stroke patients, 89.4% experienced an IS, co-existing with TIAs in 27.7% and hemorrhagic strokes in 6.2%; initial stroke events occurred ≤65 years of age in 71% of patients. CADASIL-Stroke patients (vs. CADASIL-non-Stroke) had higher cardiovascular and neurological (migraines, cognitive impairment, epilepsy/seizures, mood disorders) burden. In age- and comorbidity-adjusted models, males had higher associated risk of stroke onset (OR: 1.37, CI: 1.01–1.86). Mortality risk was higher for males (OR: 2.72, CI: 1.53–4.84).DiscussionEarly screening and targeted treatment strategies are warranted to help CADASIL patients with symptom management and risk mitigation. |
Author | Potter, Thomas McCullough, Louise D. Bako, Abdulaziz Pan, Alan P. Tannous, Jonika Seshadri, Sudha Vahidy, Farhaan S. |
AuthorAffiliation | 2 Department of Neurosurgery, Houston Methodist , Houston, TX , United States 1 Center for Health Data Science and Analytics, Houston Methodist , Houston, TX , United States 3 Glenn Biggs Institute for Alzheimer’s and Neurodegenerative Diseases, University of Texas Health Science Center , San Antonio, TX , United States 4 Department of Neurology, McGovern Medical School, University of Texas Health Science Center , Houston, TX , United States 5 Department of Population Health Sciences, Weill Cornell Medicine , New York, NY , United States |
AuthorAffiliation_xml | – name: 3 Glenn Biggs Institute for Alzheimer’s and Neurodegenerative Diseases, University of Texas Health Science Center , San Antonio, TX , United States – name: 5 Department of Population Health Sciences, Weill Cornell Medicine , New York, NY , United States – name: 1 Center for Health Data Science and Analytics, Houston Methodist , Houston, TX , United States – name: 2 Department of Neurosurgery, Houston Methodist , Houston, TX , United States – name: 4 Department of Neurology, McGovern Medical School, University of Texas Health Science Center , Houston, TX , United States |
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Cites_doi | 10.1016/B978-0-12-803058-5.00122-3 10.1093/brain/awh282 10.3389/fneur.2021.756887 10.1038/383707a0 10.3389/fnagi.2020.00091 10.1212/WNL.0b013e31824d586c 10.1111/j.1600-0404.2008.01015.x 10.1371/journal.pone.0234797 10.1212/WNL.0000000000201720 10.1136/jnnp.2004.051847 10.1161/STROKEAHA.111.631028 10.1161/hs0102.100885 10.1016/j.jstrokecerebrovasdis.2015.12.006 10.1212/WNL.96.15_supplement.2437 10.1186/s12916-017-0778-8 10.1007/s00415-014-7533-2 10.1002/ana.410440506 10.1007/s10072-023-06773-1 10.1016/S1474-4422(09)70127-9 10.1111/ane.12266 10.1111/ene.14183 |
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Copyright | Copyright © 2023 Pan, Potter, Bako, Tannous, Seshadri, McCullough and Vahidy. Copyright © 2023 Pan, Potter, Bako, Tannous, Seshadri, McCullough and Vahidy. 2023 Pan, Potter, Bako, Tannous, Seshadri, McCullough and Vahidy |
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Keywords | CADASIL risk factors vascular malformation sex differences stroke prevalence |
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References_xml | – start-page: 630 volume-title: Primer on Cerebrovascular Diseases year: 2017 ident: ref13 article-title: CADASIL doi: 10.1016/B978-0-12-803058-5.00122-3 – volume: 127 start-page: 2533 year: 2004 ident: ref12 article-title: Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients publication-title: Brain doi: 10.1093/brain/awh282 – volume: 12 start-page: 12 year: 2021 ident: ref15 article-title: Sex differences in cerebral small vessel disease: a systematic review and Meta-analysis publication-title: Front Neurol doi: 10.3389/fneur.2021.756887 – volume: 383 start-page: 707 year: 1996 ident: ref3 article-title: Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia publication-title: Nature doi: 10.1038/383707a0 – year: 2021 ident: ref17 – volume: 12 start-page: 91 year: 2020 ident: ref9 article-title: Clinical and genetic aspects of CADASIL publication-title: Front Aging Neurosci doi: 10.3389/fnagi.2020.00091 – volume: 78 start-page: 1025 year: 2012 ident: ref6 article-title: The minimum prevalence of CADASIL in Northeast England publication-title: Neurology doi: 10.1212/WNL.0b013e31824d586c – volume: 118 start-page: 291 year: 2008 ident: ref11 article-title: Psychiatric disturbances in CADASIL: a brief review publication-title: Acta Neurol Scand doi: 10.1111/j.1600-0404.2008.01015.x – volume: 15 start-page: e0234797 year: 2020 ident: ref4 article-title: Clinical and imaging features of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and cysteine-sparing NOTCH3 mutations publication-title: PLoS One doi: 10.1371/journal.pone.0234797 – volume: 100 start-page: 766 year: 2023 ident: ref24 article-title: Genetic causes of cerebral small vessel diseases: a practical guide for neurologists publication-title: Neurology doi: 10.1212/WNL.0000000000201720 – volume: 76 start-page: 739 year: 2005 ident: ref5 article-title: The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.2004.051847 – volume: 43 start-page: 137 year: 2012 ident: ref16 article-title: Effects of gender on the phenotype of CADASIL publication-title: Stroke doi: 10.1161/STROKEAHA.111.631028 – volume: 33 start-page: 67 year: 2002 ident: ref21 article-title: Cerebral microbleeds in CADASIL: a gradient-Echo magnetic resonance imaging and autopsy study publication-title: Stroke doi: 10.1161/hs0102.100885 – volume: 25 start-page: e53 year: 2016 ident: ref22 article-title: Successful use of intravenous tissue plasminogen activator as treatment for a patient with cerebral autosomal dominant Arteriopathy with subcortical infarcts and leukoencephalopathy: a case report and review of literature publication-title: J Stroke Cerebrovasc Dis doi: 10.1016/j.jstrokecerebrovasdis.2015.12.006 – year: 2023 ident: ref2 – ident: ref23 – volume: 96 start-page: 2437 year: 2021 ident: ref26 article-title: Characterization of a large single-site USA CADASIL cohort (2437) publication-title: Neurology doi: 10.1212/WNL.96.15_supplement.2437 – volume-title: GeneReviews® year: 1993 ident: ref14 article-title: CADASIL – volume: 15 start-page: 41 year: 2017 ident: ref18 article-title: Cerebral autosomal dominant Arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects publication-title: BMC Med doi: 10.1186/s12916-017-0778-8 – volume: 262 start-page: 134 year: 2015 ident: ref8 article-title: CADASIL in Central Italy: a retrospective clinical and genetic study in 229 patients publication-title: J Neurol doi: 10.1007/s00415-014-7533-2 – year: 2011 ident: ref1 – volume: 44 start-page: 731 year: 1998 ident: ref10 article-title: The phenotypic spectrum of CADASIL: clinical findings in 102 cases publication-title: Ann Neurol doi: 10.1002/ana.410440506 – start-page: 1 year: 2023 ident: ref20 article-title: Antiplatelet use and CADASIL: a retrospective observational analysis publication-title: Neurol Sci doi: 10.1007/s10072-023-06773-1 – volume: 8 start-page: 643 year: 2009 ident: ref19 article-title: Cadasil publication-title: Lancet Neurol doi: 10.1016/S1474-4422(09)70127-9 – volume: 130 start-page: 197 year: 2014 ident: ref7 article-title: Changing clinical patterns and increasing prevalence in CADASIL publication-title: Acta Neurol Scand doi: 10.1111/ane.12266 – volume: 27 start-page: 909 year: 2020 ident: ref25 article-title: Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European academy of neurology publication-title: Euro J Neurol doi: 10.1111/ene.14183 |
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SubjectTerms | CADASIL Neurology risk factors sex differences stroke prevalence vascular malformation |
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Title | Lifelong cerebrovascular disease burden among CADASIL patients: analysis from a global health research network |
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