Evidence map›Paper›PMID 38775192›Full record

ArticleAnnals of clinical and translational neurology2024

Association of serum Spp1 levels with disease progression in ALS and SBMA.

Woohee Ju, Jae-Jun Ban, Hye-Ryeong Im, Sun Hi Ko, Jaewoo Seo, Young Gi Min, Yoon-Ho Hong, Seok-Jin Choi, Jung-Joon Sung

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Context-dependent roles of osteopontin in aging-related neurological disorders.The Journal of international medical research · 2026
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  6. The role ofFrontiers in neuroscience · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Woohee JuDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-0522-1956
Jae-Jun BanDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.
Hye-Ryeong ImDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.
Sun Hi KoDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.
Jaewoo SeoDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.
Young Gi MinDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0003-0930-5997
Yoon-Ho HongDepartment of Translational Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-3325-6358
Seok-Jin ChoiDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0001-6444-977X
Jung-Joon SungDepartment of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0001-7525-5313

Funding

National Research Foundation of Korea 2018R1A5A2025964National Research Foundation of Korea 2020R1C1C1005122
6 · The paper itself

Abstract

objectiveIn comparison with amyotrophic lateral sclerosis (ALS), the contribution of neuroinflammation in spinobulbar muscular atrophy (SBMA) has been less explored. We investigated the role of neuroinflammation in the pathogenesis of ALS and SBMA by analyzing systemic inflammatory markers and osteopontin (Spp1).

methodsThis study involved 105 ALS, 77 SBMA, and 55 healthy controls. We measured their systemic inflammatory markers, serum Spp1, and cytokine levels (interferon-γ, interleukin [IL]-1β, IL-6, IL-8, IL-10, tumor necrosis factor-α, and IL-17A), investigated correlations between Spp1 levels and clinical features, and evaluated ALS survival rates according to Spp1 levels.

resultsIn the ALS group, systemic inflammatory markers were significantly higher than in the control and SBMA groups. Spp1 levels were observed to be higher in ALS patients, but the difference was not statistically significant among the study groups. Cytokine profiles were comparable. In ALS, higher Spp1 levels were correlated with lower ALS Functional Rating Scale-Revised (ALSFRS-R) scores (r = -0.25, p = 0.02) and faster disease progression rate (r = 0.37, p < 0.001). After adjusting for other prognostic indicators, high Spp1 levels were independently associated with shorter survival in ALS patients (hazard ratio 13.65, 95% confidence interval 2.57-72.53, p < 0.01).

interpretationNeuroinflammation does not appear to be a primary contributor to the pathogenesis of SBMA. Serum Spp1 levels may serve as a reliable biomarker for disease progression and prognosis in ALS. These findings expand our understanding of these two distinct motor neuron disorders and offer a potential biomarker for future studies.

Indexed as

Amyotrophic Lateral SclerosisDisease ProgressionOsteopontinAdultAgedBiomarkersCytokinesFemaleHumansMaleMiddle AgedNeuroinflammatory DiseasesBiomarkersCytokinesOsteopontinSPP1 protein, human

Identifiers

PMID38775192
PMCPMC11251464

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.