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  1. Article ; Online: Searching for Neuronal Antibodies in Psychiatric Diseases: Uncertain Findings and Implications.

    Guasp, Mar / Dalmau, Josep

    Neurology

    2023  Volume 101, Issue 15, Page(s) 656–660

    Abstract: In recent years, neurology and psychiatry journals have been inundated with reports on individual symptoms of autoimmune encephalitis (AE) that are described as distinct entities such as autoimmune psychosis, obsessive-compulsive disorders, or depression. ...

    Abstract In recent years, neurology and psychiatry journals have been inundated with reports on individual symptoms of autoimmune encephalitis (AE) that are described as distinct entities such as autoimmune psychosis, obsessive-compulsive disorders, or depression. It is unquestionable that for AE the demonstration of antibodies against neuronal-surface proteins is intrinsically linked to distinct disorders (some defining new diseases) that are usually treatment-responsive and associate with comorbidities that vary according to the antigen. By contrast, for psychiatric diseases, the apparent detection of antibodies has not defined any disorder or affected the diagnosis and treatment of patients. Although these studies frequently use anti-N-methyl-D-aspartate receptor encephalitis to rationalize the findings, they rarely adopt the same rigorous investigations or address the clinical and pathogenic significance of the antibodies or discuss the limitations related to the biological sample or antibody-testing techniques. It is imperative to consider (1) some antibodies (GAD65, TPO) occur in serum of 8%-13% of healthy people; (2) VGKC antibodies are not useful unless LGI1 or CASPR2 are investigated; (3) commercial-clinical testing for Ma2, Zic4, and SOX1 antibodies causes a high number of false-positive results; (4) GlyR antibodies have unclear disease specificity when examined only in serum; and (5) the significance of antibodies against unknown antigens of endothelium, astrocytes, myelin fibers, or granule cells of hippocampus and cerebellum is questioned by the lack of disease specificity and appropriate controls. These limitations and problems are a frequent cause of neurologic consultations. Here we discuss some of these problems, emphasizing the importance of clinical judgment over antibody findings.
    MeSH term(s) Humans ; Nerve Tissue Proteins ; Autoantibodies ; Mental Disorders/diagnosis ; Membrane Proteins ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis
    Chemical Substances Nerve Tissue Proteins ; Autoantibodies ; Membrane Proteins
    Language English
    Publishing date 2023-06-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 207147-2
    ISSN 1526-632X ; 0028-3878
    ISSN (online) 1526-632X
    ISSN 0028-3878
    DOI 10.1212/WNL.0000000000207486
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Author Response: Clinical, Neuroimmunologic, and CSF Investigations in First Episode Psychosis.

    Guasp, Mar / Dalmau, Josep

    Neurology

    2022  Volume 98, Issue 21, Page(s) 906

    MeSH term(s) Humans ; Neuroimmunomodulation ; Psychotic Disorders
    Language English
    Publishing date 2022-05-31
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 207147-2
    ISSN 1526-632X ; 0028-3878
    ISSN (online) 1526-632X
    ISSN 0028-3878
    DOI 10.1212/WNL.0000000000200724
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Author Response: Neurofilament Light Chain Levels in Anti-NMDAR Encephalitis and Primary Psychiatric Psychosis.

    Guasp, Mar / Dalmau, Josep

    Neurology

    2022  Volume 99, Issue 11, Page(s) 490

    MeSH term(s) Anti-N-Methyl-D-Aspartate Receptor Encephalitis/complications ; Humans ; Intermediate Filaments ; Psychotic Disorders/etiology
    Language English
    Publishing date 2022-09-10
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 207147-2
    ISSN 1526-632X ; 0028-3878
    ISSN (online) 1526-632X
    ISSN 0028-3878
    DOI 10.1212/WNL.0000000000201181
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Author Response: Clinical, Neuroimmunologic, and CSF Investigations in First Episode Psychosis.

    Dalmau, Josep / Guasp, Mar / Graus, Francesc

    Neurology

    2021  Volume 97, Issue 21, Page(s) 1010

    MeSH term(s) Humans ; Neuroimmunomodulation ; Psychotic Disorders/diagnosis
    Language English
    Publishing date 2021-11-22
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 207147-2
    ISSN 1526-632X ; 0028-3878
    ISSN (online) 1526-632X
    ISSN 0028-3878
    DOI 10.1212/WNL.0000000000012899
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  5. Article ; Online: Higher Solar Irradiance Is Associated With a Lower Incidence of Coronavirus Disease 2019.

    Guasp, Mar / Laredo, Carlos / Urra, Xabier

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2020  Volume 71, Issue 16, Page(s) 2269–2271

    Abstract: We studied the relationship between the incidence of coronavirus disease 2019 (COVID-19), demographical, and climatological measurements in different regions across the world. Lower solar irradiance and higher population density were independent ... ...

    Abstract We studied the relationship between the incidence of coronavirus disease 2019 (COVID-19), demographical, and climatological measurements in different regions across the world. Lower solar irradiance and higher population density were independent predictors of greater COVID-19 outbreaks. Further studies on the potential protective effect of sunlight over COVID-19 are warranted.
    MeSH term(s) COVID-19/epidemiology ; COVID-19/mortality ; Climate ; Global Health/statistics & numerical data ; Humans ; Incidence ; Population Density ; SARS-CoV-2 ; Sunlight ; Ultraviolet Rays
    Keywords covid19
    Language English
    Publishing date 2020-04-22
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1093/cid/ciaa575
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  6. Article ; Online: Encephalitis associated with antibodies against the NMDA receptor.

    Guasp, Mar / Dalmau, Josep

    Medicina clinica

    2017  Volume 151, Issue 2, Page(s) 71–79

    Abstract: The encephalitis associated with antibodies against the N-methyl-D-aspartate receptor (NMDAR) is characterized by the presence of antibodies against the GluN1 subunit of this receptor, resulting in symptoms that are similar to those observed in models of ...

    Title translation Encefalitis por anticuerpos contra el receptor de NMDA.
    Abstract The encephalitis associated with antibodies against the N-methyl-D-aspartate receptor (NMDAR) is characterized by the presence of antibodies against the GluN1 subunit of this receptor, resulting in symptoms that are similar to those observed in models of genetic or pharmacologic reduction of NMDARs. Patients are usually young adults, predominantly women, and children who develop, in a sequential manner, rapidly progressive symptoms including psychosis, abnormal movements, autonomic dysfunction, and coma. Epileptic seizures are variable and can occur throughout the course of the disease. The disease is often mistaken as viral encephalitis, primary psychiatric disorders, drug abuse, or neuroleptic malignant syndrome. About 50% of young women have an ovarian teratoma; in young girls and men the presence of a tumour is infrequent. In some patients, the disease is triggered by herpes simplex encephalitis. The recognition of anti-NMDAR encephalitis is important because, despite its severity, most patients respond to immunotherapy.
    MeSH term(s) Anti-N-Methyl-D-Aspartate Receptor Encephalitis/diagnosis ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/immunology ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/psychology ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/therapy ; Child ; Diagnosis, Differential ; Encephalitis, Viral/complications ; Encephalitis, Viral/diagnosis ; Female ; Humans ; Male ; Mental Disorders/diagnosis ; Neuroleptic Malignant Syndrome/diagnosis ; Ovarian Neoplasms/complications ; Prognosis ; Receptors, N-Methyl-D-Aspartate/immunology ; Seizures/etiology ; Sex Factors ; Substance-Related Disorders/diagnosis ; Teratoma/complications ; Young Adult
    Chemical Substances Receptors, N-Methyl-D-Aspartate
    Language Spanish
    Publishing date 2017-11-26
    Publishing country Spain
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 411607-0
    ISSN 1578-8989 ; 0025-7753
    ISSN (online) 1578-8989
    ISSN 0025-7753
    DOI 10.1016/j.medcli.2017.10.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Neurological, psychiatric, and sleep investigations after treatment of anti-leucine-rich glioma-inactivated protein 1 (LGI1) encephalitis in Spain: a prospective cohort study.

    Muñoz-Lopetegi, Amaia / Guasp, Mar / Prades, Laia / Martínez-Hernández, Eugenia / Rosa-Justícia, Mireia / Patricio, Víctor / Armangué, Thaís / Rami, Lorena / Borràs, Roger / Castro-Fornieles, Josefina / Compte, Albert / Gaig, Carles / Santamaria, Joan / Dalmau, Josep

    The Lancet. Neurology

    2024  Volume 23, Issue 3, Page(s) 256–266

    Abstract: Background: Anti-leucine-rich glioma-inactivated protein 1 (LGI1) encephalitis is an autoimmune disorder that can be treated with immunotherapy, but the symptoms that remain after treatment have not been well described. We aimed to characterise the ... ...

    Abstract Background: Anti-leucine-rich glioma-inactivated protein 1 (LGI1) encephalitis is an autoimmune disorder that can be treated with immunotherapy, but the symptoms that remain after treatment have not been well described. We aimed to characterise the clinical features of patients with anti-LGI1 encephalitis for 1 year starting within the first year after initial immunotherapy.
    Methods: For this prospective cohort study, we recruited patients with anti-LGI1 encephalitis as soon as possible after they had received conventional immunotherapy for initial symptoms; patients were recruited from 21 hospitals in Spain. Patients were excluded if they had an interval of more than 1 year since initial immunotherapy, had pre-existing neurodegenerative or psychiatric disorders, or were unable to travel to Hospital Clínic de Barcelona (Barcelona, Spain). Patients visited Hospital Clínic de Barcelona on three occasions-the first at study entry (visit 1), the second 6 months later (visit 2), and the third 12 months after the initial visit (visit 3). They underwent neuropsychiatric and videopolysomnography assessments at each visit. Healthy participants who were matched for age and sex and recruited from Hospital Clínic de Barcelona underwent the same investigations at study entry and at 12 months. Cross-sectional comparisons of clinical features between groups were done with conditional logistic regression, and binary logistic regression was used to assess associations between cognitive outcomes at 12 months and clinical features before initial immunotherapy and at study entry.
    Findings: Between May 1, 2019, and Sept 30, 2022, 42 participants agreed to be included in this study. 24 (57%) participants had anti-LGI1 encephalitis (mean age 63 years [SD 12]; 13 [54%] were female and 11 [46%] were male) and 18 (43%) were healthy individuals (mean age 62 years [10]; 11 [61%] were female and seven [39%] were male). At visit 1 (median 88 days [IQR 67-155] from initiation of immunotherapy), all 24 patients had one or more symptoms; 20 (83%) patients had cognitive deficits, 20 (83%) had psychiatric symptoms, 14 (58%) had insomnia, 12 (50%) had rapid eye movement (REM)-sleep behaviour disorder, nine (38%) had faciobrachial dystonic seizures, and seven (29%) had focal onset seizures. Faciobrachial dystonic seizures were unnoticed in four (17%) of 24 patients and focal onset seizures were unnoticed in five (21%) patients. At visit 1, videopolysomnography showed that 19 (79%) patients, but no healthy participants, had disrupted sleep structure (p=0·013); 15 (63%) patients and four (22%) healthy participants had excessive fragmentary myoclonus (p=0·039), and nine (38%) patients, but no healthy participants, had myokymic discharges (p=0·0051). These clinical and videopolysomnographic features led to additional immunotherapy in 15 (63%) of 24 patients, which resulted in improvement of these features in all 15 individuals. However, at visit 3, 13 (65%) of 20 patients continued to have cognitive deficits. Persistent cognitive deficits at visit 3 were associated with no use of rituximab before visit 1 (odds ratio [OR] 4·0, 95% CI 1·5-10·7; p=0·0015), REM sleep without atonia at visit 1 (2·2, 1·2-4·2; p=0·043), and presence of LGI1 antibodies in serum at visit 1 (11·0, 1·1-106·4; p=0·038).
    Interpretation: Unsuspected but ongoing clinical and videopolysomnography alterations are common in patients with anti-LGI1 encephalitis during the first year or more after initial immunotherapy. Recognising these alterations is important as they are treatable, can be used as outcome measures in clinical trials, and might influence cognitive outcome.
    Funding: Fundació La Caixa.
    MeSH term(s) Female ; Humans ; Male ; Middle Aged ; Autoantibodies ; Cross-Sectional Studies ; Encephalitis/immunology ; Encephalitis/therapy ; Intracellular Signaling Peptides and Proteins ; Leucine/therapeutic use ; Prospective Studies ; Retrospective Studies ; Seizures/drug therapy ; Sleep ; Spain ; Immunotherapy ; Autoimmune Diseases of the Nervous System/immunology ; Autoimmune Diseases of the Nervous System/therapy
    Chemical Substances Autoantibodies ; Intracellular Signaling Peptides and Proteins ; Leucine (GMW67QNF9C) ; LGI1 protein, human
    Language English
    Publishing date 2024-02-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 2081241-3
    ISSN 1474-4465 ; 1474-4422
    ISSN (online) 1474-4465
    ISSN 1474-4422
    DOI 10.1016/S1474-4422(23)00463-5
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  8. Article ; Online: Thyrotoxic Psychosis Associated With Amiodarone.

    Baldaquí, Nuria / Anmella, Gerard / Gómez-Ramiro, Marta / Guasp, Mar / Mesa, Alex / Parellada, Eduard

    Journal of clinical psychopharmacology

    2021  Volume 41, Issue 3, Page(s) 342–344

    MeSH term(s) Amiodarone/administration & dosage ; Amiodarone/adverse effects ; Anti-Arrhythmia Agents/administration & dosage ; Anti-Arrhythmia Agents/adverse effects ; Humans ; Male ; Middle Aged ; Psychoses, Substance-Induced/diagnosis ; Psychoses, Substance-Induced/etiology ; Thyrotoxicosis/chemically induced ; Thyrotoxicosis/diagnosis
    Chemical Substances Anti-Arrhythmia Agents ; Amiodarone (N3RQ532IUT)
    Language English
    Publishing date 2021-03-18
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 604631-9
    ISSN 1533-712X ; 0271-0749
    ISSN (online) 1533-712X
    ISSN 0271-0749
    DOI 10.1097/JCP.0000000000001375
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  9. Article ; Online: Clinical features of seronegative, but CSF antibody-positive, anti-NMDA receptor encephalitis.

    Guasp, Mar / Módena, Yasmina / Armangue, Thaís / Dalmau, Josep / Graus, Francesc

    Neurology(R) neuroimmunology & neuroinflammation

    2020  Volume 7, Issue 2

    Abstract: Objective: To determine the frequency of anti-NMDA receptor encephalitis without detectable serum NMDAR antibodies and to compare the clinical features of these patients with those with NMDAR antibodies in serum and CSF.: Methods: This is a ... ...

    Abstract Objective: To determine the frequency of anti-NMDA receptor encephalitis without detectable serum NMDAR antibodies and to compare the clinical features of these patients with those with NMDAR antibodies in serum and CSF.
    Methods: This is a retrospective assessment of serum antibody status and clinical features of 489 patients with anti-NMDAR encephalitis, defined by the presence of NMDAR antibodies in the CSF, and available paired serum/CSF samples examined at Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona, between January 2007 and December 2017. NMDAR antibodies were determined with rat brain immunostaining, in-house cell-based assay (CBA), and a commercial CBA. Patients were considered seronegative if NMDAR antibodies were undetectable with the 3 indicated techniques.
    Results: Serum NMDAR antibodies were not detected in 75 of 489 (15%) patients. Compared with the 414 seropositive patients, the seronegative were older (23.5 years [interquartile range (IQR): 17-43] vs 20.5 [IQR: 14-31];
    Conclusions: NMDAR antibodies are not detected in the serum of 15% of the patients with anti-NMDAR encephalitis. These patients appear to be older and have milder neurologic symptoms with less frequency of tumors.
    MeSH term(s) Adolescent ; Adult ; Age Factors ; Animals ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/blood ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/cerebrospinal fluid ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/epidemiology ; Anti-N-Methyl-D-Aspartate Receptor Encephalitis/physiopathology ; Autoantibodies/blood ; Autoantibodies/cerebrospinal fluid ; Female ; Humans ; Male ; Middle Aged ; Neoplasms/complications ; Neoplasms/epidemiology ; Rats ; Retrospective Studies ; Young Adult
    Chemical Substances Autoantibodies
    Language English
    Publishing date 2020-01-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2767740-0
    ISSN 2332-7812 ; 2332-7812
    ISSN (online) 2332-7812
    ISSN 2332-7812
    DOI 10.1212/NXI.0000000000000659
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: MOG Antibodies Restricted to CSF in Children With Inflammatory CNS Disorders.

    Olivé-Cirera, Gemma / Bruijstens, Arlette L / Fonseca, Elianet G / Chen, Li-Wen / Caballero, Eva / Martinez-Hernandez, Eugenia / Guasp, Mar / Sepúlveda, Maria / Naranjo, Laura / Ruiz-García, Raquel / Blanco, Yolanda / Saiz, Albert / Dalmau, Josep O / Armangue, Thaís

    Neurology

    2024  Volume 102, Issue 7, Page(s) e209199

    Abstract: Objectives: To assess the clinical significance of myelin oligodendrocyte glycoprotein antibodies (MOG-abs) restricted to CSF in children with inflammatory CNS disorders.: Methods: Patients included 760 children (younger than 18 years) from 3 ... ...

    Abstract Objectives: To assess the clinical significance of myelin oligodendrocyte glycoprotein antibodies (MOG-abs) restricted to CSF in children with inflammatory CNS disorders.
    Methods: Patients included 760 children (younger than 18 years) from 3 multicenter prospective cohort studies: (A) acquired demyelinating syndromes, including acute disseminated encephalomyelitis (ADEM); (B) non-ADEM encephalitis; and (C) noninflammatory neurologic disorders. For all cases, paired serum/CSF samples were systematically examined using brain immunohistochemistry and live cell-based assays.
    Results: A total of 109 patients (14%) had MOG-abs in serum or CSF: 79 from cohort A, 30 from B, and none from C. Of these, 63 (58%) had antibodies in both samples, 37 (34%) only in serum, and 9 (8%) only in CSF. Children with MOG-abs only in CSF were older than those with MOG-abs only in serum or in both samples (median 12 vs 6 vs 5 years,
    Discussion: Detection of MOG-abs in serum or CSF is associated with CNS inflammatory disorders. Children with MOG-abs restricted to CSF are more likely to have CSF oligoclonal bands and multiple sclerosis than those with MOG-abs detectable in serum.
    MeSH term(s) Child ; Humans ; Oligoclonal Bands ; Prospective Studies ; Central Nervous System Diseases ; Antibodies ; Multiple Sclerosis ; Encephalomyelitis, Acute Disseminated
    Chemical Substances Oligoclonal Bands ; Antibodies
    Language English
    Publishing date 2024-03-06
    Publishing country United States
    Document type Multicenter Study ; Journal Article
    ZDB-ID 207147-2
    ISSN 1526-632X ; 0028-3878
    ISSN (online) 1526-632X
    ISSN 0028-3878
    DOI 10.1212/WNL.0000000000209199
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