Peripheral Inflammation Is Associated with Dopaminergic Degeneration in Parkinson's Disease

ABSTRACT Background Peripheral inflammatory immune responses are suggested to play a major role in dopaminergic degeneration in Parkinson's disease (PD). The neutrophil‐to‐lymphocyte ratio (NLR) is a well‐established biomarker of systemic inflammation in PD. Degeneration of the nigrostriatal do...

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Published inMovement disorders Vol. 38; no. 5; pp. 755 - 763
Main Authors Muñoz‐Delgado, Laura, Labrador‐Espinosa, Miguel Ángel, Macías‐García, Daniel, Jesús, Silvia, Benítez Zamora, Belén, Fernández‐Rodríguez, Paula, Adarmes‐Gómez, Astrid D., Reina Castillo, María Isabel, Castro‐Labrador, Sandra, Silva‐Rodríguez, Jesús, Carrillo, Fátima, García Solís, David, Grothe, Michel J., Mir, Pablo
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.05.2023
Wiley Subscription Services, Inc
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Summary:ABSTRACT Background Peripheral inflammatory immune responses are suggested to play a major role in dopaminergic degeneration in Parkinson's disease (PD). The neutrophil‐to‐lymphocyte ratio (NLR) is a well‐established biomarker of systemic inflammation in PD. Degeneration of the nigrostriatal dopaminergic system can be assessed in vivo using [123I]FP‐CIT single photon emission computed tomography imaging of striatal dopamine transporter (DAT) density. Objectives To assess the relationship between the peripheral immune profile (NLR, lymphocytes, and neutrophils) and striatal DAT density in patients with PD. Methods We assessed clinical features, the peripheral immune profile, and striatal [123I]FP‐CIT DAT binding levels of 211 patients with PD (primary‐cohort). Covariate‐controlled associations between the immune response and striatal DAT levels were assessed using linear regression analyses. For replication purposes, we also studied a separate cohort of 344 de novo patients with PD enrolled in the Parkinson's Progression Markers Initiative (PPMI‐cohort). Results A higher NLR was significantly associated with lower DAT levels in the caudate (primary‐cohort: β = −0.01, p < 0.001; PPMI‐cohort: β = −0.05, p = 0.05) and the putamen (primary‐cohort: β = −0.05, p = 0.02; PPMI‐cohort: β = −0.06, p = 0.02). Intriguingly, a lower lymphocyte count was significantly associated with lower DAT levels in both the caudate (primary‐cohort: β = +0.09, p < 0.05; PPMI‐cohort: β = +0.11, p = 0.02) and the putamen (primary‐cohort: β = +0.09, p < 0.05, PPMI‐cohort: β = +0.14, p = 0.01), but an association with the neutrophil count was not consistently observed (caudate; primary‐cohort: β = −0.05, p = 0.02; PPMI‐cohort: β = 0, p = 0.94; putamen; primary‐cohort: β = −0.04, p = 0.08; PPMI‐cohort: β = −0.01, p = 0.73). Conclusions Our findings across two independent cohorts suggest a relationship between systemic inflammation and dopaminergic degeneration in patients with PD. This relationship was mainly driven by the lymphocyte count. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Bibliography:Relevant conflicts of interest/financial disclosures
The authors declare no actual or potential conflicts of interest. This work was supported by the Spanish Ministry of Science and Innovation (RTC2019‐007150‐1), the Instituto de Salud Carlos III‐Fondo Europeo de Desarrollo Regional (ISCIII‐FEDER) (PI16/01575, PI18/01898, PI19/01576, PI20/00613, PI21/01875, PI22/01704), the Consejería de Economía, Innovación, Ciencia y Empleo de la Junta de Andalucía (CVI‐02526, CTS‐7685), the Consejería de Salud y Bienestar Social de la Junta de Andalucía (PI‐0471‐2013, PE‐0210‐2018, PI‐0459‐2018, PE‐0186‐2019), the Consejería de Transformación Económica, Industria, Conocimiento y Universidades de la Junta de Andalucía (PY20_00896), and the Fundación Alicia Koplowitz. Several authors of this publication are members of the European Reference Network for Rare Neurological Diseases (project ID 739510). L.M.D. and P.M.R. are members of the COST Action IMMUPARKNET (CA21117). L.M.D. was supported by the “Río Hortega” program (CM21/00051) from the Instituto de Salud Carlos III. M.A.L.E was supported by a PhD scholarship (PIF/VI‐PPIT‐US). D.M.G. was supported by the “Juan Rodés” program (JR22/00073) rom the Instituto de Salud Carlos III. S.J. was supported by the “Acción B Clínicos Investigadores” program from the Conejería de Salud y Familias de la Junta de Andalucía (B‐0007‐2019). M.I.R.C. was supported by a PFIS fellowship (FI21/00160), J.S.R. was supported by the “Sara Borrell” program (CD21/00067), M.J.G. was supported by the “Miguel Servet” program (CP19/00031), all from the Instituto de Salud Carlos III.
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0885-3185
1531-8257
DOI:10.1002/mds.29369