Genetic and nongenetic factors for contralateral progression of unilateral moyamoya disease: the first report from the SUPRA Japan Study Group

Author:

Mineharu Yohei1,Takagi Yasushi2,Koizumi Akio3,Morimoto Takaaki4,Funaki Takeshi1,Hishikawa Tomohito5,Araki Yoshio6,Hasegawa Hitoshi7,Takahashi Jun C.8,Kuroda Satoshi9,Houkin Kiyohiro10,Miyamoto Susumu1

Affiliation:

1. Department of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto;

2. Department of Neurosurgery, Tokushima University Graduate School of Medicine, Tokushima;

3. Social Health Welfare Medicine Laboratory, Kyoto;

4. Department of Neurosurgery, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki;

5. Okayama University Graduate School of Medicine, Okayama;

6. Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya;

7. Department of Neurosurgery, Brain Research Institute, Niigata University, Niigata;

8. Department of Neurosurgery, National Cerebral and Cardiovascular Center, Suita;

9. Department of Neurosurgery, Toyama University Graduate School of Medicine, Toyama; and

10. Department of Neurological Cell Therapy, Hokkaido University Graduate School of Medicine, Sapporo, Japan

Abstract

OBJECTIVE Although many studies have analyzed risk factors for contralateral progression in unilateral moyamoya disease, they have not been fully elucidated. The aim of this study was to examine whether genetic factors as well as nongenetic factors are involved in the contralateral progression. METHODS The authors performed a multicenter cohort study in which 93 cases with unilateral moyamoya disease were retrospectively reviewed. The demographic features, RNF213 R4810K mutation, lifestyle factors such as smoking and drinking, past medical history, and angiographic findings were analyzed. A Cox proportional hazards model was used to find risk factors for contralateral progression. RESULTS Contralateral progression was observed in 24.7% of cases during a mean follow-up period of 72.2 months. Clinical characteristics were not significantly different between 67 patients with the R4810K mutation and those without it. Cox regression analysis showed that the R4810K mutation (hazard ratio [HR] 4.64, p = 0.044), childhood onset (HR 7.21, p < 0.001), male sex (HR 2.85, p = 0.023), and daily alcohol drinking (HR 4.25, p = 0.034) were independent risk factors for contralateral progression. CONCLUSIONS These results indicate that both genetic and nongenetic factors are associated with contralateral progression of unilateral moyamoya disease. The findings would serve to help us better understand the pathophysiology of moyamoya disease and to manage patients more appropriately.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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