Evidence map›Paper›PMID 31833018›Full record

ArticleJournal of molecular neuroscience : MN2020

Analysis of Cerebrospinal Fluid Soluble TREM2 and Polymorphisms in Sporadic Parkinson's Disease in a Chinese Population.

Guoyou Peng, Jiewen Qiu, Hanqun Liu, Miaomiao Zhou, Shuxuan Huang, Wenyuan Guo, Yuwan Lin, Xiang Chen, Zhe Li, Guihua Li and 9 more

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Integration of TSPO PET and fluid biomarkers to assess neuroinflammation in Parkinson's disease.European journal of nuclear medicine and molecular imaging · 2026
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  14. Association between Cerebrospinal Fluid SolubleJournal of clinical medicine · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Guoyou PengDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Jiewen QiuDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Hanqun LiuDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Miaomiao ZhouDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Shuxuan HuangDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Wenyuan GuoDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Yuwan LinDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Xiang ChenDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Zhe LiDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Guihua LiDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Wenlong ZhangDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Yunlong ZhangDepartment of Physiology, Guangzhou Medical University, Guangzhou, 511436, China.
Xingjian LiDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Zhuohua WuDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China.
Lei WeiDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
Xinling YangDepartment of Neurology, The Second Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011, China.
Xiaoqin ZhuDepartment of Physiology, Guangzhou Medical University, Guangzhou, 511436, China. whzhuxiaoqin@163.com.
Mingshu MoDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China. momingshu123@163.com.
Pingyi XuDepartment of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511436, China. pingyixu@sina.com.ORCID http://orcid.org/0000-0001-8716-5892
First Affiliated Hospital of Guangzhou Medical University · CNGuangzhou Medical University · CNSun Yat-sen University · CNXinjiang Medical University · CN

Funding

National Natural Science Foundation of China 81430021
6 · The paper itself

Abstract

backgroundTriggering receptor expressed on myeloid cells 2 (TREM2) is a microglial surface receptor that mediates the degradation disorder of amyloid β (Aβ) in Alzheimer's disease. However, the role of TREM2 in Parkinson's disease (PD) and α-Synclein (α-Syn) degradation is largely unknown.

methodsIn this case-control study on Chinese population, we sequenced for polymorphisms in exon 2 of the TREM2 gene in 1,292 individuals, PD cases (n = 612), healthy controls (n = 680) by Sanger sequence, and compared the distribution of allelic frequencies between the two groups by the Fisher's exact test. Additionally, we developed and used the enzyme-linked immunosorbent assay to evaluated soluble TREM2 (sTREM2) levels in the cerebrospinal fluid (CSF), and plasma in partial of sequenced groups (55 PD and 40 healthy controls) analyzed their relationship with total a-syn (t-a-Syn).

resultsTwo novel variants were detected in exon 2 of the TREM2 gene, namely, p.S81 N, p.G58D; however, these were not significantly associated with PD (612 PD and 680 healthy controls). sTREM2 in CSF was significantly upregulated in PD patients compared to healthy controls (433.1 ± 24.7 pg/mL vs. 275.2 ± 17.9 pg/mL, p < 0.0001), but not in plasma (281.7 ± 29.3 pg/mL vs. 257.8 ± 16.5 pg/mL, p = 0.805). In PD patients, sTREM2 was positively correlated with t-α-syn (r = 0.62, p = 0.0001) in CSF, but not in plasma (r = 0.02, p = 0.89).

conclusionsAlthough it may not indicate that exon 2 polymorphisms of TREM2 play a role in the pathogenesis of PD in the Chinese population, our findings described above highlight the relevance of CSF sTREM2 as a promising biomarker and are extremely possible to the therapeutic target for PD in the future.

Indexed as

Polymorphism, Single NucleotideBiomarkersChinaFemaleHumansMaleMembrane GlycoproteinsMiddle AgedParkinson DiseaseReceptors, ImmunologicBiomarkersMembrane GlycoproteinsReceptors, ImmunologicTREM2 protein, humanParkinson’s diseaseSoluble TREM2TREM2 polymorphismsα-Synuclein

Identifiers

PMID31833018
OpenAlexW2995258347

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Registered trials

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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.