Cargando…

Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium

OBJECTIVE: To examine the utility of the peripheral blood neutrophil-to-lymphocyte ratio (NLR) and monocyte-to-lymphocyte ratio (MLR) as biomarkers of prognosis in seropositive autoimmune encephalitis (AE). METHODS: In this multicenter study, we retrospectively analyzed 57 cases of seropositive AE w...

Descripción completa

Detalles Bibliográficos
Autores principales: Broadley, James, Wesselingh, Robb, Seneviratne, Udaya, Kyndt, Chris, Beech, Paul, Buzzard, Katherine, Nesbitt, Cassie, D’Souza, Wendyl, Brodtmann, Amy, Kalincik, Tomas, Butzkueven, Helmut, O’Brien, Terence J., Monif, Mastura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840591/
https://www.ncbi.nlm.nih.gov/pubmed/33519810
http://dx.doi.org/10.3389/fimmu.2020.597858
_version_ 1783643610570293248
author Broadley, James
Wesselingh, Robb
Seneviratne, Udaya
Kyndt, Chris
Beech, Paul
Buzzard, Katherine
Nesbitt, Cassie
D’Souza, Wendyl
Brodtmann, Amy
Kalincik, Tomas
Butzkueven, Helmut
O’Brien, Terence J.
Monif, Mastura
author_facet Broadley, James
Wesselingh, Robb
Seneviratne, Udaya
Kyndt, Chris
Beech, Paul
Buzzard, Katherine
Nesbitt, Cassie
D’Souza, Wendyl
Brodtmann, Amy
Kalincik, Tomas
Butzkueven, Helmut
O’Brien, Terence J.
Monif, Mastura
author_sort Broadley, James
collection PubMed
description OBJECTIVE: To examine the utility of the peripheral blood neutrophil-to-lymphocyte ratio (NLR) and monocyte-to-lymphocyte ratio (MLR) as biomarkers of prognosis in seropositive autoimmune encephalitis (AE). METHODS: In this multicenter study, we retrospectively analyzed 57 cases of seropositive AE with hospital admissions between January 2008 and June 2019. The initial full blood examination was used to determine each patients’ NLR and MLR. The modified Rankin Scale (mRS) was utilized to assess the patients’ follow-up disability at 12 months and then at final follow-up. Primary outcomes were mortality and mRS, while secondary outcomes were failure of first line treatment, ICU admission, and clinical relapse. Univariate and multivariable regression analysis was performed. RESULTS: During initial hospital admission 44.7% of patients had unsuccessful first line treatment. After a median follow-up of 700 days, 82.7% had good functional outcome (mRS ≤2) while five patients had died. On multivariable analysis, high NLR was associated with higher odds of first line treatment failure (OR 1.32, 95% CI 1.03–1.69, p = 0.029). Increased MLR was not associated with any short or long-term outcome. CONCLUSIONS: NLR on initial hospital admission blood tests may be provide important prognostic information for cases of seropositive AE. This study demonstrates the potential use of NLR as a prognostic marker in the clinical evaluation of patients with seropositive AE.
format Online
Article
Text
id pubmed-7840591
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-78405912021-01-29 Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium Broadley, James Wesselingh, Robb Seneviratne, Udaya Kyndt, Chris Beech, Paul Buzzard, Katherine Nesbitt, Cassie D’Souza, Wendyl Brodtmann, Amy Kalincik, Tomas Butzkueven, Helmut O’Brien, Terence J. Monif, Mastura Front Immunol Immunology OBJECTIVE: To examine the utility of the peripheral blood neutrophil-to-lymphocyte ratio (NLR) and monocyte-to-lymphocyte ratio (MLR) as biomarkers of prognosis in seropositive autoimmune encephalitis (AE). METHODS: In this multicenter study, we retrospectively analyzed 57 cases of seropositive AE with hospital admissions between January 2008 and June 2019. The initial full blood examination was used to determine each patients’ NLR and MLR. The modified Rankin Scale (mRS) was utilized to assess the patients’ follow-up disability at 12 months and then at final follow-up. Primary outcomes were mortality and mRS, while secondary outcomes were failure of first line treatment, ICU admission, and clinical relapse. Univariate and multivariable regression analysis was performed. RESULTS: During initial hospital admission 44.7% of patients had unsuccessful first line treatment. After a median follow-up of 700 days, 82.7% had good functional outcome (mRS ≤2) while five patients had died. On multivariable analysis, high NLR was associated with higher odds of first line treatment failure (OR 1.32, 95% CI 1.03–1.69, p = 0.029). Increased MLR was not associated with any short or long-term outcome. CONCLUSIONS: NLR on initial hospital admission blood tests may be provide important prognostic information for cases of seropositive AE. This study demonstrates the potential use of NLR as a prognostic marker in the clinical evaluation of patients with seropositive AE. Frontiers Media S.A. 2021-01-14 /pmc/articles/PMC7840591/ /pubmed/33519810 http://dx.doi.org/10.3389/fimmu.2020.597858 Text en Copyright © 2021 Broadley, Wesselingh, Seneviratne, Kyndt, Beech, Buzzard, Nesbitt, D’Souza, Brodtmann, Kalincik, Butzkueven, O’Brien, Monif and Australian Autoimmune Encephalitis Consortium http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Broadley, James
Wesselingh, Robb
Seneviratne, Udaya
Kyndt, Chris
Beech, Paul
Buzzard, Katherine
Nesbitt, Cassie
D’Souza, Wendyl
Brodtmann, Amy
Kalincik, Tomas
Butzkueven, Helmut
O’Brien, Terence J.
Monif, Mastura
Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium
title Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium
title_full Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium
title_fullStr Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium
title_full_unstemmed Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium
title_short Peripheral Immune Cell Ratios and Clinical Outcomes in Seropositive Autoimmune Encephalitis: A Study by the Australian Autoimmune Encephalitis Consortium
title_sort peripheral immune cell ratios and clinical outcomes in seropositive autoimmune encephalitis: a study by the australian autoimmune encephalitis consortium
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840591/
https://www.ncbi.nlm.nih.gov/pubmed/33519810
http://dx.doi.org/10.3389/fimmu.2020.597858
work_keys_str_mv AT broadleyjames peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT wesselinghrobb peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT seneviratneudaya peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT kyndtchris peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT beechpaul peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT buzzardkatherine peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT nesbittcassie peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT dsouzawendyl peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT brodtmannamy peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT kalinciktomas peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT butzkuevenhelmut peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT obrienterencej peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT monifmastura peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium
AT peripheralimmunecellratiosandclinicaloutcomesinseropositiveautoimmuneencephalitisastudybytheaustralianautoimmuneencephalitisconsortium