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      Central and Peripheral Nervous System Complications of Vasculitis Syndromes from Pathology to Bedside: Part 2—Peripheral Nervous System

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          Abstract

          Purpose of Review

          Peripheral nervous system vasculitides (PNSV) are a heterogeneous group of disorders with a clinical subset that may differ in prognosis and therapy. We provide a comprehensive update on the clinical assessment, diagnosis, complications, treatment, and follow-up of PNSV.

          Recent Findings

          Progress in neuroimaging, molecular testing, and peripheral nerve biopsy has improved clinical assessment and decision-making of PNSV, also providing novel insights on how to prevent misdiagnosis and increase diagnostic certainty. Advances in imaging techniques, allowing to clearly display the vessel walls, have also enhanced the possibility to differentiate inflammatory from non-inflammatory vascular lesions, while recent histopathology data have identified the main morphological criteria for more accurate diagnosis and differential diagnoses. Overall, the identification of peculiar morphological findings tends to improve diagnostic accuracy by defining a clearer boundary between systemic and non-systemic neuropathies. Therefore, the definition of epineurium vessel wall damage, type of vascular lesion, characterization of lymphocyte populations, antibodies, and inflammatory factors, as well as the identification of direct nerve damage or degeneration, are the common goals for pathologists and clinicians, who will both benefit for data integration and findings translation. Nevertheless, to date, treatment is still largely empiric and, in some cases, unsatisfactory, thus often precluding precise prognostic prediction. In this context, new diagnostic techniques and multidisciplinary management will be essential in the proper diagnosis and prompt management of PNSV, as highlighted in the present review.

          Summary

          Thirty to fifty percent of all patients with vasculitis have signs of polyneuropathy. Neuropathies associated with systemic vasculitis are best managed according to the guidelines of the underlying disease because appropriate workup and initiation of treatment can reduce morbidity. Steroids, or in severe or progressive cases, cyclophosphamide pulse therapy is the standard therapy in non-systemic vasculitic neuropathies. Some patients need long-term immunosuppression. The use of novel technologies for high-throughput genotyping will permit to determine the genetic influence of related phenotypes in patients with PNSV.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s11910-023-01249-3.

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          Most cited references112

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          2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides.

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            Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

            A key public health need is to identify individuals at high risk for a given disease to enable enhanced screening or preventive therapies. Because most common diseases have a genetic component, one important approach is to stratify individuals based on inherited DNA variation. 1 Proposed clinical applications have largely focused on finding carriers of rare monogenic mutations at several-fold increased risk. Although most disease risk is polygenic in nature, 2–5 it has not yet been possible to use polygenic predictors to identify individuals at risk comparable to monogenic mutations. Here, we develop and validate genome-wide polygenic scores for five common diseases. The approach identifies 8.0%, 6.1%, 3.5%, 3.2% and 1.5% of the population at greater than three-fold increased risk for coronary artery disease (CAD), atrial fibrillation, type 2 diabetes, inflammatory bowel disease, and breast cancer, respectively. For CAD, this prevalence is 20-fold higher than the carrier frequency of rare monogenic mutations conferring comparable risk. 6 We propose that it is time to contemplate the inclusion of polygenic risk prediction in clinical care and discuss relevant issues.
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              Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

              Crohn’s disease (CD) and ulcerative colitis (UC), the two common forms of inflammatory bowel disease (IBD), affect over 2.5 million people of European ancestry with rising prevalence in other populations 1 . Genome-wide association studies (GWAS) and subsequent meta-analyses of CD and UC 2,3 as separate phenotypes implicated previously unsuspected mechanisms, such as autophagy 4 , in pathogenesis and showed that some IBD loci are shared with other inflammatory diseases 5 . Here we expand knowledge of relevant pathways by undertaking a meta-analysis of CD and UC genome-wide association scans, with validation of significant findings in more than 75,000 cases and controls. We identify 71 new associations, for a total of 163 IBD loci that meet genome-wide significance thresholds. Most loci contribute to both phenotypes, and both directional and balancing selection effects are evident. Many IBD loci are also implicated in other immune-mediated disorders, most notably with ankylosing spondylitis and psoriasis. We also observe striking overlap between susceptibility loci for IBD and mycobacterial infection. Gene co-expression network analysis emphasizes this relationship, with pathways shared between host responses to mycobacteria and those predisposing to IBD.
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                Author and article information

                Contributors
                gelsomina.mansueto@unicampania.it , mansueto.g@inwind.it
                glanza@oasi.en.it
                shabo1@inwind.it
                pasquale_orabona@yahoo.it
                DAAlaouieh@salud.unm.edu
                EmHong@salud.unm.edu
                girolamisara97@gmail.com
                marco.montella@unicampania.it
                drfrancescofisicaro@gmail.com
                anna.galdieri@policliniconapoli.it
                puneetpalsingh@pbi.ac.in
                mariodinapoli@katamail.com
                Journal
                Curr Neurol Neurosci Rep
                Curr Neurol Neurosci Rep
                Current Neurology and Neuroscience Reports
                Springer US (New York )
                1528-4042
                1534-6293
                23 February 2023
                : 1-25
                Affiliations
                [1 ]GRID grid.9841.4, ISNI 0000 0001 2200 8888, Department of Advanced Medical and Surgical Sciences (DAMSS), , University of Campania “Luigi Vanvitelli”, ; Piazza L. Miraglia 2, 80138 Naples, Italy
                [2 ]GRID grid.9841.4, ISNI 0000 0001 2200 8888, Clinical Department of Laboratory Services and Public Health—Legal Medicine Unit, , University of Campania “Luigi Vanvitelli”, ; Via Luciano Armanni 5, 80138 Naples, Italy
                [3 ]GRID grid.4691.a, ISNI 0000 0001 0790 385X, Pathology-Unit of Federico II University, ; Via S. Pansini 3, 80131 Naples, Italy
                [4 ]GRID grid.8158.4, ISNI 0000 0004 1757 1969, Department of Surgery and Medical-Surgical Specialties, , University of Catania, ; Via Santa Sofia 78, 95123 Catania, Italy
                [5 ]GRID grid.419843.3, ISNI 0000 0001 1250 7659, Clinical Neurophysiology Research Unit, , Oasi Research Institute-IRCCS, ; Via Conte Ruggero 73, 94018 Troina, Italy
                [6 ]Pathology Unit, Sant’Anna E San Sebastiano Hospital, 81100 Caserta, Italy
                [7 ]GRID grid.266832.b, ISNI 0000 0001 2188 8502, School of Medicine, , University of New Mexico, ; Albuquerque, NM USA
                [8 ]Neurological Service, SS Annunziata Hospital, Viale Mazzini 100, 67039 Sulmona, L’Aquila Italy
                [9 ]GRID grid.9841.4, ISNI 0000 0001 2200 8888, Mental and Physical Health and Preventive Medicine Department, , University of Campania “Luigi Vanvitelli”, ; Via Luciano Armanni 5, 80138 Naples, Italy
                [10 ]GRID grid.8158.4, ISNI 0000 0004 1757 1969, Department of Biomedical and Biotechnological Sciences, , University of Catania, ; Via Santa Sofia 97, 95123 Catania, Italy
                [11 ]AOU “Luigi Vanvitelli”, Via Santa Maria Di Costantinopoli 104, 80138 Naples, Italy
                [12 ]GRID grid.412580.a, ISNI 0000 0001 2151 1270, Department of Human Genetics, , Punjabi University, ; Patiala, 147002 Punjab India
                Author information
                http://orcid.org/0000-0002-0544-5100
                http://orcid.org/0000-0002-5659-662X
                http://orcid.org/0000-0001-9427-320X
                http://orcid.org/0000-0001-7508-5414
                http://orcid.org/0000-0002-2064-6568
                http://orcid.org/0000-0002-6516-9136
                http://orcid.org/0000-0003-0302-2291
                http://orcid.org/0000-0002-8588-7653
                http://orcid.org/0000-0002-1579-8807
                http://orcid.org/0000-0001-5600-2986
                http://orcid.org/0000-0003-2154-4261
                http://orcid.org/0000-0001-9609-4926
                Article
                1249
                10.1007/s11910-023-01249-3
                9947450
                36820992
                35054c0f-59b6-40de-b020-7b0b35f7b324
                © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 18 January 2023
                Categories
                Article

                Neurosciences
                peripheral nerves,vasculitides,physiopathology,antineutrophil cytoplasmic antibodies,differential diagnoses,management,treatment,glucocorticoid,cyclophosphamide

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