Evidence map›Paper›PMID 30353300›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2019

High-sensitivity C-reactive protein and high mobility group box-1 levels in Parkinson's disease.

Aslıhan Baran, Mahmut Bulut, Mehmet Cemal Kaya, Özlem Demirpençe, Bünyamin Sevim, Eşref Akıl, Sefer Varol

Abstract read
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Cell-Free DNA and Mitochondria in Parkinson's Disease.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Article
  8. Early diagnosis of Parkinson's disease: biomarker study.Frontiers in aging neuroscience · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
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  18. Article
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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

7 authors at 3 institutions in 2 countries.

Aslıhan BaranDepartment of Neurology, Park Hospital, Malatya, Turkey.
Mahmut BulutDepartment of Biochemistry, Faculty of Medicine, Dicle University, 21280, Diyarbakır, Turkey. drmahmutbulut@yahoo.com.ORCID http://orcid.org/0000-0002-6008-378X
Mehmet Cemal KayaDepartment of Biochemistry, Faculty of Medicine, Dicle University, 21280, Diyarbakır, Turkey.
Özlem DemirpençeDepartment of Biochemistry, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey.
Bünyamin SevimDepartment of Biochemistry, Faculty of Medicine, Dicle University, 21280, Diyarbakır, Turkey.
Eşref AkılDepartment of Neurology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey.
Sefer VarolDepartment of Neurology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey.
Dicle University · TRMalatya Devlet Hastanesi · TRSivas Cumhuriyet Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various immunologic and inflammatory factors are contributed to pathogenesis of Parkinson's disease (PD). High mobility group box-1 (HMGB1) is a protein that plays certain roles in inflammation, DNA repair, transcription, somatic recombination, cell differentiation, cell migration, neuronal development, and neurodegeneration. The aim of the present study was to evaluate the serum levels of HMGB1 and high-sensitivity C-reactive protein (hs-CRP) among patients with Parkinson's disease and healthy controls. This study includes 30 patients with PD and 30 healthy controls, matched sex, age, body mass index, and smoking status. HMGB1 and hs-CRP serum levels were compared between the groups. The diagnostic performance of HMGB1 and hs-CRP was evaluated with receiver operating characteristic (ROC) curve analysis. HMGB1 levels were significantly higher in PD patients than in controls. Hs-CRP levels were significantly higher in PD patients than in controls There was a moderate correlation between hs-CRP and HMGB1 levels in the patient group. The cut-off value of HMGB1 level for the prediction of PD was determined as 32.8 ng/mL with 80% sensitivity and 60% specificity (p = 0.006). The cut-off value of hs-CRP level for the prediction of PD was determined as 0.63 mg/L with 66.7% sensitivity and 77.7% specificity (p = 0.007). This study demonstrates for the first time the association between HMGB1, hs-CRP, and PD. We found that HMGB1 and hs-CRP levels to be significantly higher in the PD patients than in the normal controls. As a result of the ROC curve analysis, HMGB1 and hs-CRP levels may be fair markers in the diagnosis of PD.

Indexed as

AgedAged, 80 and overBiomarkersC-Reactive ProteinCross-Sectional StudiesFemaleHMGB1 ProteinHumansMaleMiddle AgedParkinson DiseaseROC CurveBiomarkersC-Reactive ProteinHMGB1 ProteinHMGB1 protein, humanHigh mobility group box-1High-sensitivity C-reactive proteinInflammationParkinson’s disease

Identifiers

PMID30353300
OpenAlexW2898451964

What OpenQuestion holds

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Registered trials

None linked

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.