Evidence map›Paper›PMID 36976478›Full record

ArticleMolecular neurobiology2023

Ganglioside-focused Glycan Array Reveals Abnormal Anti-GD1b Auto-antibody in Plasma of Preclinical Huntington's Disease.

Tien-Wei Lin, Jung-Kai Chang, Yih-Ru Wu, Tsung-Hsien Sun, Yang-Yu Cheng, Chien-Tai Ren, Mei-Hung Pan, Jin-Lin Wu, Kuo-Hsuan Chang, Hwai-I Yang and 3 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Serum antibody screening using glycan arrays.Chemical Society reviews · 2024
    Review
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

13 authors at 3 institutions in 1 country.

Tien-Wei Lin *Genomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Jung-Kai Chang *Genomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Yih-Ru WuDepartment of Neurology, Linkou Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Tsung-Hsien SunGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Yang-Yu ChengGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Chien-Tai RenGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Mei-Hung PanGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Jin-Lin WuGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Kuo-Hsuan ChangDepartment of Neurology, Linkou Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Hwai-I YangGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan.
Chiung-Mei ChenDepartment of Neurology, Linkou Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taoyuan, Taiwan. cmchen@adm.cgmh.org.tw.
Chung-Yi WuGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan. cyiwu@icloud.com.
Yun-Ru ChenGenomics Research Center, Academia Sinica, Taipei, 115, Taiwan. yrchen@gate.sinica.edu.tw.ORCID http://orcid.org/0000-0002-6596-6338
Genomics Research Center, Academia Sinica · TWChang Gung University · TWChina Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Huntington's disease (HD) is a progressive and devastating neurodegenerative disease marked by inheritable CAG nucleotide expansion. For offspring of HD patients carrying abnormal CAG expansion, biomarkers that predict disease onset are crucially important but still lacking. Alteration of brain ganglioside patterns has been observed in the pathology of patients carrying HD. Here, by using a novel and sensitive ganglioside-focused glycan array, we examined the potential of anti-glycan auto-antibodies for HD. In this study, we collected plasma from 97 participants including 42 control (NC), 16 pre-manifest HD (pre-HD), and 39 HD cases and measured the anti-glycan auto-antibodies by a novel ganglioside-focused glycan array. The association between plasma anti-glycan auto-antibodies and disease progression was analyzed using univariate and multivariate logistic regression. The disease-predictive capacity of anti-glycan auto-antibodies was further investigated by receiver operating characteristic (ROC) analysis. We found that anti-glycan auto-antibodies were generally higher in the pre-HD group when compared to the NC and HD groups. Specifically, anti-GD1b auto-antibody demonstrated the potential for distinguishing between pre-HD and control groups. Moreover, in combination with age and the number of CAG repeat, the level of anti-GD1b antibody showed excellent predictability with an area under the ROC curve (AUC) of 0.95 to discriminate between pre-HD carriers and HD patients. With glycan array technology, this study demonstrated abnormal auto-antibody responses that showed temporal changes from pre-HD to HD.

Indexed as

Huntington DiseaseNeurodegenerative DiseasesBiomarkersBrainHumansBiomarkersAuto-antibodyGangliosidesGD1bGlycan arrayHuntington’s diseasePre-HD

Identifiers

PMID36976478
OpenAlexW4361190182

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.