YAO Ming, ZHOU Li-Xin, ZHU Yi-Cheng, PENG Bin, NI Jun. Topographic Characteristic and Clinical Significance of Cerebral Microbleeds in Patients with CADASIL[J]. Chinese Journal of Stroke, 2020, 15(04): 343-348.
[1] CHABRIAT H,JOUTEL A,DICHGANS M,et al.CADASIL[J]. Lancet Neurol,2009,8(7):643-653.[2] LEE Y C,LIU C S,CHANG M H,et al.Population-specific spectrum of NOTCH3 mutations,MRI features and founder effect of CADASIL inChinese[J]. J Neurol,2009,256(2):249-255.[3] WARDLAW J M,SMITH E E,BIESSELS G J,etal. Neuroimaging standards for research into smallvessel disease and its contribution to ageing andneurodegeneration[J]. Lancet Neurol,2013,12(8):822-838.[4] GREENBERG S M,VERNOOIJ M W,CORDONNIER C,et al. Cerebral microbleeds:aguide to detection and interpretation[J]. LancetNeurol,2009,8(2):165-174.[5] FAZEKAS F,KLEINERT R,ROOB G,et al.变有关。CAA是CMBs的另一常见病因。大量研究表明CAA与皮层/皮层下CMBs密切相关,CMBs是CAA病变进展的影像标志之一[4,20]。APOE 基因型与CAA患者CMBs形成相关[5],并影响其在颅内的分布。目前尚缺乏大样本的关于CADASIL基因型与CMBs分布部位的相关研究,但是有个例报道大量脑桥融合性CMBs见于P1008S突变的CADASIL患者[21],而全脑大量弥漫分布的CMBs见于R558C纯合突变患者[22]。因此,我们推测NOTCH3 基因突变可能影响CMBs在CADASIL的分布,有待于进一步大样本的基因型-影像表型分析。本研究也存在以下不足。首先,本研究数据来自单中心,存在一定的偏移,但是所有CADASIL患者为连续入组,并随机选择性别匹配的高血压小动脉硬化患者,降低了可能的偏移。其次,患者接受T2*或者SWI检查,SWI对于CMBs的检出率高于T2*,但是两组不同MR序列的比例相同,减少了可能的误差。最后,本研究未进行NOTCH3 基因型与CMBs分布特征的关联分析。未来研究将系统进行两者的关联性分析,探索CADASIL患者发生脑CMBs可能的遗传机制。Histopathologic analysis of foci of signal losson gradient-echo T2*-weighted MR images inpatients with spontaneous intracerebral hemorrhage:evidence of microangiopathy-related microbleeds[J].AJNR Am J Neuroradiol,1999,20(4):637-642.[6] SMITH E E,GREENBERG S M. Clinical diagnosisof cerebral amyloid angiopathy:validation of theBoston criteria[J]. Curr Atheroscler Rep,2003,5(4):260-266.[7] ROMERO J R,PREIS S R,BEISER A,eta1. Risk factors,stroke prevention treatments,and prevalence of cerebral microbleeds in theFramingham Heart Study[J]. Stroke,2014,45(5):1492-1494.[8] POELS M M,VERNOOIJ M W,IKRAM M A,et al.Prevalence and risk factors of cerebral microbleeds:an update of the Rotterdam scan study[J]. Stroke,2010,41(10 Suppl):S103-S106.[9] DIEHGANS M,HOLTMANNSPOTTERM,HERZOG J,et a1. Cerebral microbleeds inCADASIL:a gradient-echo magnetic resonanceimaging and autopsy study[J]. Stroke,2002,33(1):67-71.[10] LESNIK OBERSTEIN S A,VAN DEN BOOM R,VAN BUCHEM M A,et a1. Cerebral microbleeds inCADASIL[J]. Neurology,2001,57(6):1066-1070.[11] VISWANATHAN A,GUICHARD J P,GSCHWENDTNER A,et al. Blood pressureand haemoglobin A1c are associated withmicrohaemorrhage in CADASIL:a two-centrecohort study[J]. Brain,2006,129(Pt 9):2375-2383.[12] VAN DEN BOOM R,LESNIK OBERSTEINS A,FERRARI M D,et al. Cerebral autosomaldominant arteriopathy with subcortical infarctsand leukoencephalopathy:MR imaging findings atdifferent ages-3rd-6th decades[J]. Radiology,2003,229(3):683-690.[13] NANNUCCI S,RINNOCI V,PRACUCCI G,etal. Location,number and factors associated withcerebral microbleeds in an Italian-British cohort ofCADASIL patients[J/OL]. PLoS One,2018,13(1):e0190878[2019-12-15]. https://Doi. org/10. 1371/journal. pone. 0190878.[14] LEE J S,KO K,OH J H,et al. Cerebral microbleeds,hypertension,and intracerebral hemorrhage incerebral autosomal-dominant arteriopathy withsubcortical infarcts and leukoencephalopathy[J].Front Neurol,2017,8:203.[15] 王婉,任志霞,夏明,等. CADASIL患者脑微出血的临床研究[J]. 中华神经科杂志,2018,51(9):712-716.
[16] RUTTEN J W,VAN EIJSDEN B J,DUERINGM,et al. The effect of NOTCH3 pathogenic variantposition on CADASIL disease severity:NOTCH3EGFr 1-6 pathogenic variant are associated with amore severe phenotype and lower survival comparedwith EGFr 7-34 pathogenic variant[J]. Genet Med,2019,21(3):676-682.[17] MUIÑO E,GALLEGO-FABREGA C,CULLELLN,et al. Systematic review of cysteine-sparingNOTCH3 missense mutations in patients withclinical suspicion of CADASIL[J/OL]. Int J Mol Sci,2017,18(9):E1964[2019-12-15]. https://doi.org/10.3390/ijms18091964.[18] TANG S C,CHEN Y R,CHI N F,et al. Prevalenceand clinical characteristics of stroke patients with p.R544C NOTCH3 mutation in Taiwan[J]. Ann ClinTransl Neurol,2018,6(1):121-128.[19] LEE J S,KANG C H,PARK S Q,et al. Clinicalsignificance of cerebral microbleeds locations inCADASIL with R544C NOTCH3 mutation[J/OL].PLoS One,2015,10(2):e0118163[2019-12-15].https://doi.org/10.1371/journal.pone.0118163.[20] SHOAMANESH A,KWOK C S,BENAVENTE O.Cerebral microbleeds:histopathological correlationof neuroimaging[J]. Cerebrovasc Dis,2011,32(6):528-534.[21] OH S I,KIM S H,KIM H J. Massive pontinemicrobleeds in a patient with CADASIL[J]. JAMANeurol,2014,71(8):1048-1049.[22] ANAMNART C,SONGSAENG D,CHANPRASERT S. A large number of cerebralmicrobleeds in CADASIL patients presenting withrecurrent seizures:a case report[J]. BMC Neurol,2019,19(1):106.