Evidence map›Paper›PMID 33552238›Full record

ArticleTherapeutic advances in neurological disorders2021

VNTR2/VNTR3 genotype in the

Shengyao Su, Qing Liu, Xueping Zhang, Xinmei Wen, Lin Lei, Faxiu Shen, Zhirong Fan, Jianying Duo, Yan Lu, Li Di and 6 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in neurological disorders, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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  16. Neonatal Fc Receptor-Targeted Therapies in Neurology.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
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  18. The importance of FcRn in neuro-immunotherapies: From IgG catabolism,Therapeutic advances in neurological disorders · 2021
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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

16 authors at 1 institution in 1 country.

Shengyao SuDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-5020-7056
Qing LiuDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Chang Chun Street, Beijing, China.
Xueping ZhangDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Chang Chun Street, Beijing, China.
Xinmei WenDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Lin LeiDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Faxiu ShenDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Zhirong FanDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-3118-9016
Jianying DuoDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yan LuDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Li DiDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Min WangDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Hai ChenDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wenjia ZhuDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Min XuDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Suobin WangDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yuwei DaDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Chang Chun Street, Beijing 100053, China.
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntravenous immunoglobulin (IVIG) has been commonly used to treat myasthenia gravis exacerbation, but is still ineffective in nearly 30% of patients. A variable number of tandem repeat (VNTR) polymorphism in the

methodsThe distribution of VNTR genotypes was analyzed in 334 patients with MG. Varied VNTR alleles were determined by capillary electrophoresis and confirmed by Sanger sequencing. Information of endogenous IgG levels were collected in patients without previous immunotherapy (

resultsThe VNTR3/3 and VNTR2/3 genotypes were detected in 96.7% (323/334) and 3.4% (11/334) patients, respectively. Patients with VNTR2/3 heterozygosity had lower endogenous IgG levels than those with VNTR3/3 homozygosity (9.81 ± 2.61 g/L

conclusionThe VNTR2/3 genotype could influence endogenous IgG levels and serve as a predictive marker for poor responses to IVIG in MG patients.

Indexed as

FCGRT geneintravenous immunoglobulin treatmentmyasthenia gravisvariable number of tandem repeat polymorphism

Identifiers

PMID33552238
PMCPMC7844454
OpenAlexW3124162460

What OpenQuestion holds

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LicenceCC BY-NC
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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.