Evidence map›Paper›PMID 26217177›Full record

ArticleFrontiers in cellular neuroscience2015

Contra-Directional Expression of Serum Homocysteine and Uric Acid as Important Biomarkers of Multiple System Atrophy Severity: A Cross-Sectional Study.

Dan Chen, Xiaobo Wei, Jing Zou, Rui Wang, Xu Liu, Xiaofeng Xu, Jianjun Lu, Zhanhang Wang, Beisha Tang, Brian Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 4 pooled it
6.4field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 4 syntheses or guidelines pooled it, 49 citations in OpenAlex.

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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

12 authors at 5 institutions in 2 countries.

Dan ChenDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Xiaobo WeiDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Jing ZouDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Rui WangDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Xu LiuDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Xiaofeng XuDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Jianjun LuDepartment of Neurology, Guangdong 999 Brain Hospital , Guangzhou , China.
Zhanhang WangDepartment of Neurology, Guangdong 999 Brain Hospital , Guangzhou , China.
Beisha TangThe State Key Laboratory of Medical Genetics, Central South University , Changsha , China.
Brian WangDepartment of Pharmacology and Neuroscience, University of North Texas Health Science Center , Fort Worth, TX , USA.
Kunlin JinDepartment of Pharmacology and Neuroscience, University of North Texas Health Science Center , Fort Worth, TX , USA.
Qing WangDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University , Guangzhou , China.
Third Affiliated Hospital of Sun Yat-sen University · CNSun Yat-sen University · CNGuangdong 999 Brain Hospital · CNUniversity of North Texas · USUniversity of North Texas Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

highlightsSerum Hcy was higher in MSA patients when compared to healthy subjects, particularly in male patients.Serum UA was lower in MSA patients when compared healthy subjects, particularly in male patients.Serum Hcy levels were significantly positively correlated with the severity of MSA.The ROC curve for the combination of Hcy and UA showed potential diagnostic value in discriminating MSA from healthy subjects.

aimThere is evidence suggesting that inflammatory responses play a critical role in the pathogenesis of multiple system atrophy (MSA). Whether inflammatory mediators can be used as reliable biomarkers to detect the severity and progression of MSA remains largely unknown.

methodsWe performed a cross-sectional study that included 47 patients with MSA and 50 healthy age-matched controls. Serum levels of homocysteine (Hcy), uric acid (UA), and C-reactive protein (CRP) were measured. These levels positively correlated with the severity of MSA, based on both motor and non-motor symptoms. Several scales were used to rate the severity of MSA, including the Unified multiple system atrophy rating scale, Parkinson's disease sleep scale, Non-motor Symptoms Scale, the Schwab & England activities of daily living scale, Webster Scale, modified Hoehn and Yahr staging scale, and the Mini-Mental State Examination. Receiver operating characteristic (ROC) curves was applied to map the diagnostic accuracy of MSA against healthy subjects.

resultsCompared with healthy subjects, we found that serum Hcy was higher, UA was lower, and CRP levels were unchanged in MSA patients. These findings were especially prominent in male patients. No significant differences of serum Hcy and UA were observed between patients of MSA and PD. Interestingly, there was a significant correlation between Hcy levels and MSA severity such as movement dysfunction, declined cognition, and cardiovascular symptoms. Additionally, the ROC curve for the combination of Hcy and UA (AUC 0.736) showed potential diagnostic value in discriminating MSA from healthy subjects.

conclusionOur findings suggest that the inflammatory mediators Hcy and UA may play important roles in the pathogenesis of MSA. The measurement of serum Hcy and UA levels could then be a useful tool to accurately distinguish MSA from healthy subjects.

Indexed as

cognitionhomocysteineinflammationmultiple system atrophyuric acid

Identifiers

PMID26217177
PMCPMC4492156
OpenAlexW1602987347

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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.