Blood Pressure Elevation and Risk of Moyamoya Syndrome in Patients With Trisomy 21

Author:

Santoro Jonathan D.1,Lee Sarah1234,Mlynash Michael2,Nguyen Thuy1,Lazzareschi Daniel V.5,Kraler Lironn D.34,Mayne Elizabeth W.1,Steinberg Gary K.234

Affiliation:

1. Division of Child Neurology, Department of Neurology,

2. Division of Stroke and Neurocritical Care, Department of Neurology,

3. Departments of Neurology and

4. Neurosurgery,

5. School of Medicine, Stanford University, Stanford, California

Abstract

OBJECTIVES: Individuals with Down syndrome (DS) are at risk for the development of moyamoya syndrome (MMS); MMS is often recognized only after a resulting stroke has occurred. Our goal with this study was to determine if elevations in blood pressure (BP) precede acute presentation of MMS in individuals with DS. METHODS: A single-center, retrospective case-control study was performed. Thirty patients with MMS and DS and 116 patients with DS only were identified retrospectively. Three BP recordings were evaluated at set intervals (18–24 months, 12–18 months, and 6–12 months before diagnosis of MMS). These were then compared against control averages from patients with DS only. To assess changes over the time, we used general linear model repeated measures analysis of variance. To identify independent predictors of MMS and DS, we used a multivariable analysis using generalized estimating equations accounting for repeated measures of BP. RESULTS: BP in patients with MMS and DS rose significantly over the 24-month period preceding presentation (34th, 42nd, and 70th percentiles at the 18–24–month, 12–18–month, and 6–12–month periods, respectively). BPs in the patients with both MMS and DS were significantly higher than in the DS-only controls in the 6 to 12 (P < .001) and 12 to 18 months before presentation (P = .016). Higher Suzuki scores, bilateral disease, and posterior circulation involvement were also predictive of BP elevation before presentation. CONCLUSIONS: Elevations in BP may foreshadow presentation of MMS in individuals with DS. This simple, low-cost screening measure may lead to early identification of at-risk patients in the medical home and prevent irreversible neurologic injury.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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