Asymptomatic Moyamoya Disease: Literature Review and Ongoing AMORE Study
Recent development of a non-invasive magnetic resonance examination has increased the opportunity to identify asymptomatic patients with moyamoya disease who have experienced no cerebrovascular events. However, their clinical features, prognosis, and treatment strategy are still unclear because of s...
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| Published in | Neurologia medico-chirurgica Vol. 55; no. 3; pp. 194 - 198 |
|---|---|
| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
Japan
The Japan Neurosurgical Society
2015
THE JAPAN NEUROSURGICAL SOCIETY |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0470-8105 1349-8029 1349-8029 |
| DOI | 10.2176/nmc.ra.2014-0305 |
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| Abstract | Recent development of a non-invasive magnetic resonance examination has increased the opportunity to identify asymptomatic patients with moyamoya disease who have experienced no cerebrovascular events. However, their clinical features, prognosis, and treatment strategy are still unclear because of small number of subjects and short follow-up periods. Therefore, we have designed Asymptomatic Moyamoya Registry (AMORE) study in Japan. The objectives of this nation-wide, multi-center prospective study are to clarify long-term prognosis of asymptomatic patients with moyamoya disease and to determine the risk factors that cause ischemic and hemorrhagic stroke in them. In this article, we review the published data on asymptomatic moyamoya disease and report the on-going multi-center prospective cohort study, AMORE study. We would like to emphasize the importance to determine the clinical features, prognosis, and treatment strategies of asymptomatic moyamoya disease in very near future. |
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| AbstractList | [Abstract] Recent development of a non-invasive magnetic resonance examination has increased the opportunity to identify asymptomatic patients with moyamoya disease who have experienced no cerebrovascular events. However, their clinical features, prognosis, and treatment strategy are still unclear because of small number of subjects and short follow-up periods. Therefore, we have designed Asymptomatic Moyamoya Registry [AMORE] study in Japan. The objectives of this nation-wide, multi-center prospective study are to clarify long-term prognosis of asymptomatic patients with moyamoya disease and to determine the risk factors that cause ischemic and hemorrhagic stroke in them. In this article, we review the published data on asymptomatic moyamoya disease and report the on-going multi-center prospective cohort study, AMORE study. We would like to emphasize the importance to determine the clinical features, prognosis, and treatment strategies of asymptomatic moyamoya disease in very near future. Recent development of a non-invasive magnetic resonance examination has increased the opportunity to identify asymptomatic patients with moyamoya disease who have experienced no cerebrovascular events. However, their clinical features, prognosis, and treatment strategy are still unclear because of small number of subjects and short follow-up periods. Therefore, we have designed Asymptomatic Moyamoya Registry (AMORE) study in Japan. The objectives of this nation-wide, multi-center prospective study are to clarify long-term prognosis of asymptomatic patients with moyamoya disease and to determine the risk factors that cause ischemic and hemorrhagic stroke in them. In this article, we review the published data on asymptomatic moyamoya disease and report the on-going multi-center prospective cohort study, AMORE study. We would like to emphasize the importance to determine the clinical features, prognosis, and treatment strategies of asymptomatic moyamoya disease in very near future. |
| Author | KURODA, Satoshi Group, AMORE Study |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25739434$$D View this record in MEDLINE/PubMed |
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| References | 6) Kuroda S, Houkin K, Ishikawa T, Nakayama N, Iwasaki Y: Novel bypass surgery for moyamoya disease using pericranial flap: its impacts on cerebral hemodynamics and long-term outcome. Neurosurgery 66: 1093–1101; discussion 1101, 2010 9) Miyamoto S, Yoshimoto T, Hashimoto N, Okada Y, Tsuji I, Tominaga T, Nakagawara J, Takahashi JC; JAM Trial Investigators: Effects of extracranial-intracranial bypass for patients with hemorrhagic moyamoya disease: results of the Japan Adult Moyamoya Trial. Stroke 45: 1415–1421, 2014 12) Kuroda S, Hashimoto N, Yoshimoto T, Iwasaki Y; Research Committee on Moyamoya Disease in Japan: Radiological findings, clinical course, and outcome in asymptomatic moyamoya disease: results of multicenter survey in Japan. Stroke 38: 1430–1435, 2007 7) Kuroda S, Houkin K, Kamiyama H, Abe H, Mitsumori K: Regional cerebral hemodynamics in childhood moyamoya disease. Childs Nerv Syst 11: 584–590, 1995 14) Nanba R, Kuroda S, Takeda M, Shichinohe H, Nakayama N, Ishikawa T, Houkin K, Iwasaki Y: [Clinical features and outcomes of 10 asymptomatic adult patients with moyamoya disease]. No Shinkei Geka 31: 1291–1295, 2003 (Japanese 5) Kawaguchi S, Okuno S, Sakaki T: Effect of direct arterial bypass on the prevention of future stroke in patients with the hemorrhagic variety of moyamoya disease. J Neurosurg 93: 397–401, 2000 10) Guzman R, Lee M, Achrol A, Bell-Stephens T, Kelly M, Do HM, Marks MP, Steinberg GK: Clinical outcome after 450 revascularization procedures for moyamoya disease. Clinical article. J Neurosurg 111: 927–935, 2009 23) Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis; Health Labour Sciences Research Grant for Research on Measures for Infractable Diseases: Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis). Neurol Med Chir (Tokyo) 52: 245–266, 2012 15) Baba T, Houkin K, Kuroda S: Novel epidemiological features of moyamoya disease. J Neurol Neurosurg Psychiatr 79: 900–904, 2008 20) Kikuta K, Takagi Y, Nozaki K, Sawamoto N, Fukuyama H, Hashimoto N: The presence of multiple microbleeds as a predictor of subsequent cerebral hemorrhage in patients with moyamoya disease. Neurosurgery 62: 104–111, discussion 111–112, 2008 22) Kuroda S, Ishikawa T, Houkin K, Nanba R, Hokari M, Iwasaki Y: Incidence and clinical features of disease progression in adult moyamoya disease. Stroke 36: 2148–2153, 2005 3) Liu W, Morito D, Takashima S, Mineharu Y, Kobayashi H, Hitomi T, Hashikata H, Matsuura N, Yamazaki S, Toyoda A, Kikuta K, Takagi Y, Harada KH, Fujiyama A, Herzig R, Krischek B, Zou L, Kim JE, Kitakaze M, Miyamoto S, Nagata K, Hashimoto N, Koizumi A: Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development. PLoS ONE 6: e22542, 2011 1) Suzuki J, Takaku A: Cerebrovascular “moyamoya” disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol 20: 288–299, 1969 21) Kuroda S, Kashiwazaki D, Ishikawa T, Nakayama N, Houkin K: Incidence, locations, and longitudinal course of silent microbleeds in moyamoya disease: a prospective T2*-weighted MRI study. Stroke 44: 516–518, 2013 4) Karasawa J, Touho H, Ohnishi H, Miyamoto S, Kikuchi H: Long-term follow-up study after extracranial-intracranial bypass surgery for anterior circulation ischemia in childhood moyamoya disease. J Neurosurg 77: 84–89, 1992 13) Yamada M, Fujii K, Fukui M: [Clinical features and outcomes in patients with asymptomatic moyamoya disease—from the results of nation-wide questionnaire survey]. No Shinkei Geka 33: 337–342, 2005 (Japanese 16) Shinkawa A, Ueda K, Kiyohara Y, Kato I, Sueishi K, Tsuneyoshi M, Fujishima M: Silent cerebral infarction in a community-based autopsy series in Japan. The Hisayama Study. Stroke 26: 380–385, 1995 11) Scott RM, Smith JL, Robertson RL, Madsen JR, Soriano SG, Rockoff MA: Long-term outcome in children with moyamoya syndrome after cranial revascularization by pial synangiosis. J Neurosurg 100: 142–149, 2004 17) Ishikawa T, Kuroda S, Nakayama N, Terae S, Kudou K, Iwasaki Y: Prevalence of asymptomatic microbleeds in patients with moyamoya disease. Neurol Med Chir (Tokyo) 45: 495–500; discussion 500, 2005 8) Miyamoto S, Akiyama Y, Nagata I, Karasawa J, Nozaki K, Hashimoto N, Kikuchi H: Long-term outcome after STA-MCA anastomosis for moyamoya disease. Neurosurg Focus 5: e5, 1998 19) Kikuta K, Takagi Y, Nozaki K, Okada T, Hashimoto N: Histological analysis of microbleed after surgical resection in a patient with moyamoya disease. Neurol Med Chir (Tokyo) 47: 564–567, 2007 2) Kuroda S, Houkin K: Moyamoya disease: current concepts and future perspectives. Lancet Neurol 7: 1056–1066, 2008 18) Kikuta K, Takagi Y, Nozaki K, Hanakawa T, Okada T, Mikuni N, Miki Y, Fushmi Y, Yamamoto A, Yamada K, Fukuyama H, Hashimoto N: Asymptomatic microbleeds in moyamoya disease: T2*-weighted gradient-echo magnetic resonance imaging study. J Neurosurg 102: 470–475, 2005 11 22 12 23 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 10 21 18159142 - Neurol Med Chir (Tokyo). 2007 Dec;47(12):564-7 16247234 - Neurol Med Chir (Tokyo). 2005 Oct;45(10):495-500; discussion 500 21799892 - PLoS One. 2011;6(7):e22542 17112208 - Neurosurg Focus. 1998 Nov 15;5(5):e5 16179571 - Stroke. 2005 Oct;36(10):2148-53 5775283 - Arch Neurol. 1969 Mar;20(3):288-99 10969936 - J Neurosurg. 2000 Sep;93(3):397-401 15796381 - J Neurosurg. 2005 Mar;102(3):470-5 18077479 - J Neurol Neurosurg Psychiatry. 2008 Aug;79(8):900-4 7886710 - Stroke. 1995 Mar;26(3):380-5 22870528 - Neurol Med Chir (Tokyo). 2012;52(5):245-66 14758941 - J Neurosurg. 2004 Feb;100(2 Suppl Pediatrics):142-9 18940695 - Lancet Neurol. 2008 Nov;7(11):1056-66 17395863 - Stroke. 2007 May;38(5):1430-5 19463046 - J Neurosurg. 2009 Nov;111(5):927-35 23223508 - Stroke. 2013 Feb;44(2):516-8 15830539 - No Shinkei Geka. 2005 Apr;33(4):337-42 14719442 - No Shinkei Geka. 2003 Dec;31(12):1291-5 1607976 - J Neurosurg. 1992 Jul;77(1):84-9 8556725 - Childs Nerv Syst. 1995 Oct;11(10):584-90 18300897 - Neurosurgery. 2008 Jan;62(1):104-11, discussion 111-2 20495424 - Neurosurgery. 2010 Jun;66(6):1093-101; discussion 1101 24668203 - Stroke. 2014 May;45(5):1415-21 |
| References_xml | – reference: 12) Kuroda S, Hashimoto N, Yoshimoto T, Iwasaki Y; Research Committee on Moyamoya Disease in Japan: Radiological findings, clinical course, and outcome in asymptomatic moyamoya disease: results of multicenter survey in Japan. Stroke 38: 1430–1435, 2007 – reference: 9) Miyamoto S, Yoshimoto T, Hashimoto N, Okada Y, Tsuji I, Tominaga T, Nakagawara J, Takahashi JC; JAM Trial Investigators: Effects of extracranial-intracranial bypass for patients with hemorrhagic moyamoya disease: results of the Japan Adult Moyamoya Trial. Stroke 45: 1415–1421, 2014 – reference: 22) Kuroda S, Ishikawa T, Houkin K, Nanba R, Hokari M, Iwasaki Y: Incidence and clinical features of disease progression in adult moyamoya disease. Stroke 36: 2148–2153, 2005 – reference: 3) Liu W, Morito D, Takashima S, Mineharu Y, Kobayashi H, Hitomi T, Hashikata H, Matsuura N, Yamazaki S, Toyoda A, Kikuta K, Takagi Y, Harada KH, Fujiyama A, Herzig R, Krischek B, Zou L, Kim JE, Kitakaze M, Miyamoto S, Nagata K, Hashimoto N, Koizumi A: Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development. PLoS ONE 6: e22542, 2011 – reference: 19) Kikuta K, Takagi Y, Nozaki K, Okada T, Hashimoto N: Histological analysis of microbleed after surgical resection in a patient with moyamoya disease. Neurol Med Chir (Tokyo) 47: 564–567, 2007 – reference: 13) Yamada M, Fujii K, Fukui M: [Clinical features and outcomes in patients with asymptomatic moyamoya disease—from the results of nation-wide questionnaire survey]. No Shinkei Geka 33: 337–342, 2005 (Japanese) – reference: 4) Karasawa J, Touho H, Ohnishi H, Miyamoto S, Kikuchi H: Long-term follow-up study after extracranial-intracranial bypass surgery for anterior circulation ischemia in childhood moyamoya disease. J Neurosurg 77: 84–89, 1992 – reference: 7) Kuroda S, Houkin K, Kamiyama H, Abe H, Mitsumori K: Regional cerebral hemodynamics in childhood moyamoya disease. Childs Nerv Syst 11: 584–590, 1995 – reference: 10) Guzman R, Lee M, Achrol A, Bell-Stephens T, Kelly M, Do HM, Marks MP, Steinberg GK: Clinical outcome after 450 revascularization procedures for moyamoya disease. Clinical article. J Neurosurg 111: 927–935, 2009 – reference: 18) Kikuta K, Takagi Y, Nozaki K, Hanakawa T, Okada T, Mikuni N, Miki Y, Fushmi Y, Yamamoto A, Yamada K, Fukuyama H, Hashimoto N: Asymptomatic microbleeds in moyamoya disease: T2*-weighted gradient-echo magnetic resonance imaging study. J Neurosurg 102: 470–475, 2005 – reference: 21) Kuroda S, Kashiwazaki D, Ishikawa T, Nakayama N, Houkin K: Incidence, locations, and longitudinal course of silent microbleeds in moyamoya disease: a prospective T2*-weighted MRI study. Stroke 44: 516–518, 2013 – reference: 20) Kikuta K, Takagi Y, Nozaki K, Sawamoto N, Fukuyama H, Hashimoto N: The presence of multiple microbleeds as a predictor of subsequent cerebral hemorrhage in patients with moyamoya disease. Neurosurgery 62: 104–111, discussion 111–112, 2008 – reference: 5) Kawaguchi S, Okuno S, Sakaki T: Effect of direct arterial bypass on the prevention of future stroke in patients with the hemorrhagic variety of moyamoya disease. J Neurosurg 93: 397–401, 2000 – reference: 6) Kuroda S, Houkin K, Ishikawa T, Nakayama N, Iwasaki Y: Novel bypass surgery for moyamoya disease using pericranial flap: its impacts on cerebral hemodynamics and long-term outcome. 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| Title | Asymptomatic Moyamoya Disease: Literature Review and Ongoing AMORE Study |
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