Journal Pre-proof A challenging diagnosis of reversible “vascular” dementia: Cerebral amyloid angiopathy-related inflammation L. Poli, V. De Giuli, F. Piazza, I. Volonghi, G. Bigliardi, S. Vallone, P.F. Nichelli, R. Gasparotti, A. Zini, A. Padovani, A. Pezzini PII: S0165-5728(19)30517-X DOI: https://doi.org/10.1016/j.jneuroim.2019.577109 Reference: JNI 577109 To appear in: Journal of Neuroimmunology Received date: 6 October 2019 Revised date: 4 November 2019 Accepted date: 4 November 2019 Please cite this article as: L. Poli, V. De Giuli, F. Piazza, et al., A challenging diagnosis of reversible “vascular” dementia: Cerebral amyloid angiopathy-related inflammation, Journal of Neuroimmunology (2018), https://doi.org/10.1016/j.jneuroim.2019.577109 This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. 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Journal Pre-proof A challenging diagnosis of reversible “vascular” dementia: Cerebral Amyloid Angiopathy-related inflammation Poli L, De Giuli V, Piazza F, Volonghi I, Bigliardi G, Vallone S, Nichelli PF, Gasparotti R, Zini A, Padovani A, Pezzini A AFFILIATIONS - Neurology Unit, Spedali Civili of Brescia, Brescia, Italy (PL, VI) - Department of Clinical and Experimental Sciences, Neurology Clinic, University of Brescia, ro of Brescia, Italy (DGV, Padovani A, Pezzini A) - School of Medicine, University of Milano - Bicocca, Monza, Italy (PF) - Department of Medicine and Surgery, Radiology and Public Health, University of Brescia, Brescia, Italy (GR) Department of Neuroscience, Neurology Clinic, Stroke Unit, University of Modena and Reggio -p - Emilia, Nuovo Ospedale Civile "S.Agostino-Estense", AUSL Modena (BG, NPF) IRCCS Istituto di Scienze Neurologiche di Bologna, UOC Neurologia e Rete Stroke re - metropolitana, Ospedale Maggiore, Bologna (ZA) Department of Neuroradiology, Nuovo Ospedale Civile "S.Agostino-Estense", AUSL Modena, lP - Corresponding Author na Modena, Italy (VS) Jo ur Loris Poli, MD Neurology Unit, Spedali Civili P.le Spedali Civili, 1 25123 Brescia, Italy mail: loris.poli@gmail.com Phone number: +39 030 3995632 Abstract word count: 94 Total word count: 2555 Number of references: 17 The present manuscript includes 2 figures. Journal Pre-proof Abstract Cerebral amyloid angiopathy-related inflammation (CAA-ri) is a rare and treatable variant of CAA likely due to an autoimmune response directed toward beta-amyloid deposits. Cognitive and behavioral manifestations are the most common symptoms, followed by focal neurological signs, headache and seizures, associated with characteristics neuroradiological features on brain magnetic resonance imaging (MRI). ro of We describe the clinical course, radiological features and therapeutic approach of two patients with probable CAA-ri with the aim of emphasizing the importance of an early Jo ur na lP re memory clinics and stroke units. -p diagnosis of this potentially reversible disease in different neurological settings, such as Journal Pre-proof Introduction Cerebral amyloid angiopathy (CAA), the most common cause of lobar intracerebral hemorrhage in the elderly, is the final result of the deposition of -amyloid in the wall of small to medium sized arteries, and less frequently veins and capillaries, of the leptomeninges and brain [1-2]. Cerebral amyloid angiopathy-related inflammation (CAAri) is a rare and relatively unknown feature of CAA. It is characterized by a variable ro of combination of clinical manifestations, such as subacute confusion, cognitive decline, headache, epileptic seizures and focal neurological deficits [3], associated with characteristic neuroradiological features on brain magnetic resonance imaging (MRI) [4,5]. -p As suggested by the neuropathological evidence of vascular and perivascular re inflammation, these features are thought to be the result of an autoantibody-mediated lP inflammatory response directed toward  amyloid (A) deposited in the walls of cerebral blood vessels [5,6]. na The observation of clinical and radiological improvement of CAA-ri after administration of high dose corticosteroids or other immunosuppressive agents emphasizes the ur importance of making a correct and prompt diagnosis in clinical practice. Jo In the present report, we illustrate the clinical presentation, neuroimaging features, and outcome of two patients with probable CAA-ri (according to Auriel et al criteria) [4] who received immunosuppressive therapy. Journal Pre-proof Case 1 A 79-year-old male was admitted to the neurological ward because of rapidly-progressive neurobehavioral symptoms (aggressiveness, agitation and confusion) and gait unsteadiness, responsible for his fall and consequent head trauma. His past medical history included systemic arterial hypertension and acute intracerebral hemorrhage (ICH) involving the left temporal lobe one year before, in association with MRI evidence of cortical-subcortical microbleeds and superficial siderosis (Figure 1, Panel A), as well as a ro of 6-month history of slight memory deficits and worsening of pre-existing language impairment. Because the cerebral hematoma was not surgically evacuated at the time of -p occurrence, we made the diagnosis of probable CAA according to the modified Boston re criteria [2], after exclusion of secondary causes of ICH. On admission, the neurological examination evidenced spatial and temporal disorientation, lP psychomotor slowness, and confusion. The Mini-Mental State Examination (MMSE) score na was 8/30. Brain MRI showed bilateral T2 and fluid-attenuated inversion recovery (FLAIR) subcortical confluent hyperintensities with greater representation in the right fronto- ur parietal lobe, characterized by increased apparent diffusion coefficient, consistent with Jo vasogenic edema. T2*-weighted gradient-echo (GRE) sequences showed cortical microhemorrhages and right fronto-parietal cortical hemosiderosis, with diffuse leptomeningeal enhancement, mainly over the left hemisphere, after gadolinium administration (Figure 1, Panel B). Blood tests including erythrocyte sedimentation rate, C-reactive protein, serum protein electrophoresis, angiotensin-converting enzyme, and adenosine deaminase were normal. Cerebrospinal fuid (CSF) examination showed hyperproteinorrachia (371 mg/dL, normal range, <45 mg/dl) with normal glucose content and cell count. No bacteria, mycobacteria or fungi were detected on CSF cultures. Molecular analysis of the Apolipoprotein E gene (APOE) revealed apoE ε3/ε4 genotype. The search for CSF antiamyloid B (A) autoantibodies proved positive (at the concentration of 193.5 ng/ml) [5]. Journal Pre-proof Based on clinical and neuroimaging findings we made the diagnosis of probable CAA-ri, according to Auriel et al criteria [4]. Three weeks after hospital admission, intravenous corticosteroid therapy was started (methylprednisolone 1000 mg i.v./die for the first 3 days), followed by oral administration (prednisolone 1 mg kg/die). Because of the progressive alteration of the state of consciousness in the following days, we decided to administer intravenous cyclophosphamide (1200 mg at 3-week intervals). After a transient behavioral improvement, the patient continued to deteriorate and died 40 days after ro of symptoms onset. No postmortem examination was performed. -p Case 2 re A 76-year-old woman was admitted to the geriatric ward because of 5-day gait unsteadiness along with severe frontal and periorbital headache and rapidly progressive lP behavioral alterations (agitation and confusion). Past medical history included systemic na arterial hypertension, mild depression, amnesic mild cognitive impairment and retinal detachment involving her left eye. Two days after admission she developed acute language ur impairment with psychomotor slowing. Brain computed tomography (CT) scan showed Jo bilateral parietal convexity subarachnoid hemorrhage in addiction to diffuse bilateral cortico-subcortical hypodensity. Neurological examination showed non fluent aphasia, along with unsteady and wide-based gait. Brain MRI showed left temporo-occipital white matter hyperintensity on T2/FLAIR sequences, characterized by increased apparent diffusion coefficient and hypointensity on T1-weighted sequences, consistent with vasogenic edema while GRE revealed corticalsubcortical micro-hemorrhages along with a convexity subarachnoid hemorrhage (Figure 2, Panel A). We also detected mild leptomeningeal enhancement after gadolinium administration. To rule out either vascular anomalies or central nervous system vasculitis we performed a conventional cerebral angiography which didn’t show signs consistent Journal Pre-proof with those clinical hypotheses. Blood workup for infection and autoimmune markers resulted negative as well. CSF examination showed mildly elevated protein level (65 mg/dL, normal range <50 mg/dl) with normal glucose content and cell count, in absence of infection. Screening of APOE revealed ε3/ε4 genotype. The search for CSF anti-A autoantibodies turned out to be positive (at the concentration of 113.75 ng/ml) [5]. Clinical data together with neuroimaging findings were consistent with the diagnosis of probable CAA-ri, according to Auriel et al criteria [4]. Corticosteroid therapy with ro of methylprednisolone 1000 mg i.v./daily for the first 3 days was started, followed by prednisolone 75 mg/daily, which was gradually tapered in the following months. A few -p days after the therapy was started, a marked clinical improvement with resolution of re confusion and speech disorder was detected, and the patient returned to her premorbid state. After 4 weeks of treatment we performed a follow up brain MRI that revealed lP dramatic improvement of the white matter lesions, in addition to clear reduction of the na vasogenic edema. The 3-month follow-up MRI showed complete resolution of the Jo deficits. ur vasogenic edema (Figure 2, Panel B) along with an evident improvement on cognitive Journal Pre-proof Discussion CAA-ri is an aggressive, uncommon and likely underdiagnosed subtype of CAA. Although a definite diagnosis requires pathologic confirmation, clinical data, MRI findings, as well as response to immunosuppressive therapy are strongly suggestive of the disease [4]. Based on histopathology of brain biopsy, two forms of CAA-ri can be distinguished: inflammatory CAA (ICAA) and Amyloid--Related Angiitis (ABRA). Specifically, while ICAA is characterized by a perivascular inflammation, ABRA is characterized by ro of transmural and intramural inflammation, often with granulomas formation [7,8,10]. ICAA and ABRA share several clinical and neuroradiological features and are indistinguishable -p from each other without histopathological data [9-10]. re Both described cases showed a clinical picture characterized by rapidly progressive lP behavioural changes and cognitive dysfunction. In line with the diagnostic criteria [4], the diagnosis in the reported cases was probable CAA-ri. Detectable anti-A antibodies in the na CSF should be considered as an additional evidence in favor of this diagnosis in both patients. Indeed, as already described by Piazza and collaborators [5], CSF anti-A ur antibodies seem to be directly implicated in the pathogenesis of CAA-ri: anti-A antibody Jo titres are very high during the acute phases of the disease and decrease upon immunosuppressive treatment, when a concurrent improvement of the clinical status occurs [6,11]. Although a validation of cut-offs has not yet been performed, previous studies reported significantly higher values of CSF anti-A antibodies in subjects affected by CAA-ri compared to control subjects [5], just as in our cases. Therefore, the research of anti-A antibodies not only focuses on the possible pathogenic mechanism of the disease but also represents a possible useful biomarker for the diagnosis and non-invasive monitoring of CAA-ri [6-12]. Journal Pre-proof As already reported in the literature, most patients with CAA-ri show partial to complete response to high dose corticosteroids or other immunosuppressive agents associated with clinical and radiological improvement [13]. Some authors suggest that it may be reasonable to use empirical immunosuppressive therapy, without brain biopsy, for patients meeting the criteria proposed for probable CAA-ri [11-13]. To diagnose the disease with a high degree of certainty based only on clinical and MRI criteria would avoid an invasive brain biopsy that would aggravate the patient's discomfort and increase the risk of ro of complications. Obviously, the lack of pathological data prevents any conclusions regarding the differential diagnosis between the two disease entities ABRA and ICAA. -p Notwithstanding, both forms require prompt immunosuppression and show a similar re response to treatment [4,7,8]. In our patients the diagnosis of CAA-ri was made by using both the suggested diagnostic lP criteria [4] and the detection of anti-A antibodies on CSF. Consequently, we opted for na corticosteroids in both our cases. It is reasonable hypothesize that the delay in initiating the immunosuppressive therapy administration, along with the poor general conditions and the ur diffuse cerebral involvement, facilitated the negative outcome in the first patient, while the Jo rapid detection of the disease and the prompt initiation of specific therapy resulted in excellent clinical outcome in the second case. The two described cases have in common both the clinical presentation (cognitive and behavioral changes) and the neuroradiological features. Nevertheless, the first case had history of previous cerebral hemorrhage with a diagnosis of probable CAA, while in the second one the CAA-ri was the first manifestation of an underlying CAA. Therefore, in the case of rapidly progressive cognitive decline, it is mandatory to consider CAA-ri among the possible diagnoses, even if a clinical history suggestive of the underlying CAA is lacking; this is also applicable to patients with Alzheimer's disease, even in the mild cognitive impairment phase [14-16]. Journal Pre-proof In this scenario, brain MRI with specific sequences (FLAIR, GRE/SWI and ADC) could allow the recognition of the characteristic neuroradiological features. In particular, according to the clinico-radiological criteria for the diagnosis of CAA-ri recently proposed by Auriel and colleagues [4], both mono or bilateral white matter hyperintensities extending to the immediately subcortical white matter along with cortico-subcortical hemorrhages should be considered highly specific for CAA-ri [5], with subacute cognitive decline or seizures as the predominant clinical symptoms [17]. As regards laboratory data, ro of in addition to the detection of anti-A antibodies on CSF, the determination of the Apolipoprotein E genotype (APOE) may be considered as a further contribution to the -p diagnosis. Actually, although no specific genotype-phenotype correlations have been re established so far, the ε4 allele has been consistently reported to increase the risk of developing CAA-ri [17] a finding that provides further strength to this diagnosis in our lP cases. na In conclusion, CAA-ri is a challenging and important diagnosis to make in clinical practice, because of the potential benefits of a prompt immunosuppressive therapy (with ur steroids and other therapeutic agents) in interrupting the underlying biological process and Jo reversing the clinical symptoms and neuroradiologic involvement. Journal Pre-proof Funding Acknowledgments This work was partially supported by Fondazione Cariplo (biomarkARIA Research Project - 2015-0820); the Alzheimer’s Association (ModelCAA Research Grant - AARG-18561699); and the SINdem-CAA Study Group. Compliance with ethical standards Jo ur na lP re -p ro of Conflict of interest: None Journal Pre-proof References 1. Wermer MJH, Greenberg SM. The growing clinical spectrum of cerebral amyloid angiopathy. Curr Opin Neurol. 2018;31(1):28-35 2. Greenberg SM, Charidimou A. Diagnosis of Cerebral Amyloid Angiopathy: Evolution of the Boston Criteria. Stroke. 2018;49(2):491-497 3. Eng JA, Frosch MP, Choi K et al. Clinical manifestations of cerebral amyloid angiopathy-related inflammation. Ann Neurol. 2004;55(2):250-6. ro of 4. Auriel E, Charidimou A, Gurol ME et al. Validation of clinicoradiological criteria for the diagnosis of cerebral amyloid angiopathy-related Inflammation. JAMA -p Neurol. 2016;73:197-202 re 5. Piazza F, Greenberg SM, Savoiardo M et al. Anti-amyloid ?? autoantibodies in cerebral amyloid angiopathy-related inflammation: Implications for amyloid- lP modifying therapies. Ann Neurol. 2013;73:449-58 na 6. DiFrancesco JC, Brioschi M, Brighina L et al. Anti-A?? autoantibodies in the CSF of patient with cerebral amyloid angiopathy-related inflammation: a case report. ur Neurology. 2011;76:842-4 Jo 7. Moussaddy A, Levy A, Strbian D et al. Inflammatory cerebral amyloid angiopathy, amyloid-β-related angiitis, and primary angiitis of the central nervous system: similarities and differences. Stroke. 2015;46(9):e210-3 8. Ng DW, Magaki S, Terashima KH et al. Amyloid-β-related angiitis: a report of 2 cases with unusual presentations. Hum Pathol. 2017;64:191-197 9. Salvarani C, Morris JM, Giannini C et al. Imaging Findings of Cerebral Amyloid Angiopathy, Aβ-Related Angiitis (ABRA), and Cerebral Amyloid AngiopathyRelated Inflammation: A Single-Institution 25-Year Experience. Medicine (Baltimore). 2016;95(20):e3613 Journal Pre-proof 10. Chu S, Xu F, Su Y et al. Cerebral amyloid angiopathy (CAA)-related inflammation: comparison of inflammatory CAA and amyloid-β-related angiitis. J Alzheimers Dis. 2016;51(2):525-32 11. Charidimou A. Cerebral amyloid angiopathy-related inflammation biomarkers: Where are we Now?. J Alzheimers Dis. 2016;50(1):9-11 12. Sakaguchi H, Ueda A, Kosaka T et al. Cerebral amyloid angiopathy-related inflammation presenting with steroid- responsive higher brain dysfunction: case ro of report and review of the literature. J Neuroinflammation. 2011;8:116. 13. Kirshner HS, Bradshaw M. The inflammatory form of cerebral amyloid angiopathy re Neurosci Rep. 2015;15:54 -p or "cerebral amyloid angiopathy-related inflammation" (CAARI). Curr Neurol 14. Boncoraglio GB, Piazza F, Savoiardo M et al. Prodromal Alzheimer's disease lP presenting as cerebral amyloid angiopathy-related inflammation with spontaneous na amyloid-related imaging abnormalities and high cerebrospinal fluid anti-Aβ autoantibodies. J Alzheimers Dis. 2015;45(2):363-7 ur 15. Piazza, F, Winblad, B. Amyloid-Related Imaging Abnormalities (ARIA) in Jo Immunotherapy Trials for Alzheimer’s Disease: Need for Prognostic Biomarkers? J Alzheimers Dis. 2016;52(2):417-420. 16. Carmona-Iragui M, Fernández-Arcos A, Alcolea D, et al. Cerebrospinal Fluid AntiAmyloid-β Autoantibodies and Amyloid PET in Cerebral Amyloid AngiopathyRelated Inflammation. J Alzheimers Dis. 2016;50(1):1-7. 17. Kinnecom C, Lev MH, Wendell L et al. Course of cerebral amyloid angiopathy– related inflammation. Neurology 2007;68:1411-1416 Journal Pre-proof Fig. 1 Panel A Panel B FLAIR FLAIR FLAIR FLAIR ADC GRE GRE GRE ADC T1-MDC GRE GRE ro of FLAIR -p Brain MRI, Case 1 Panel A: FLAIR and GRE sequences performed immediately after the ICH, showed lP consistent with probable CAA re markers of cerebral small vessel disease (lobar ICH, microbleeds, superficial siderosis), na Panel B: right temporal-fronto-parietal white matter hyperintensity on FLAIR sequences characterized by increased ADC, consistent with vasogenic edema. The GRE images ur show multiple cortical- subcortical microhemorrhages and the T1-mdc diffuse Jo leptomeningeal enhancement mainly over the left hemisphere (White Arrow) Journal Pre-proof Panel A FLAIR ADC GRE Panel B ADC FLAIR FLAIR ADC GRE ADC GRE GRE ro of FLAIR Fig. 2 -p Brain MRI, Case 2 Panel A: left temporo-occipital white matter hyperintensity on FLAIR sequence re characterized by increased ADC, consistent with vasogenic edema. The GRE images lP showing cortical-subcortical microhemorrhages at the same level and the T1-mdc left na temporal leptomeningeal enhancement (White Arrow) Panel B: three months after immunosuppressive therapy, the same sequences revealed Jo edema ur dramatic improvement of the white matter lesions along with reduction of the vasogenic Journal Pre-proof Abstract Cerebral amyloid angiopathy-related inflammation (CAA-ri) is a rare and treatable variant of CAA likely due to an autoimmune response directed toward beta-amyloid deposits. Cognitive and behavioral manifestations are the most common symptoms, followed by focal neurological signs, headache and seizures, associated with characteristics neuroradiological features on brain magnetic resonance imaging (MRI). ro of We describe the clinical course, radiological features and therapeutic approach of two patients with probable CAA-ri with the aim of emphasizing he importance of an early Jo ur na lP re memory clinics and stroke units. -p diagnosis of this potentially reversible disease in different neurological settings, such as Figure 1 Figure 2