Evidence map›Paper›PMID 36172344›Full record

ArticleFrontiers in immunology2022

Vitamin D metabolism pathway polymorphisms are associated with efficacy and safety in patients under anti-PD-1 inhibitor therapy.

Jianquan Luo, Huiqing Chen, Fang Ma, Chenlin Xiao, Bao Sun, Yiping Liu, Haoneng Tang, Yue Yang, Wenhui Liu, Zhiying Luo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 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

10 authors at 2 institutions in 1 country.

Jianquan LuoDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Huiqing ChenDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Fang MaDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, China.
Chenlin XiaoDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Bao SunDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Yiping LiuDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Haoneng TangDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Yue YangDepartment of Spine Surgery, The Second Xiangya Hospital of Central South University, Changsha, China.
Wenhui LiuDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Zhiying LuoDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Second Xiangya Hospital of Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Vitamin D (VitD) signaling has been increasingly investigated for its role in stimulating the innate and adaptive immune systems and suppressing inflammatory responses. Therefore, we examined the associations between VitD-related genetic polymorphisms, plasma 25-hydroxyvitamin D (25(OH)D), and the efficacy and safety of immune checkpoint inhibitors (ICIs). Patients and methods: A total of 13 single-nucleotide polymorphisms (SNPs) in VitD metabolic pathway genes were genotyped in 343 cancer patients receiving ICI treatment using the MassARRAY platform. In 65 patients, the associations between plasma 25(OH)D levels and ICI treatment outcomes were investigated further. Results: We found that the Conclusion: In summary, our findings showed that genetic variations in the VitD metabolism pathway were associated with ICI treatment outcomes, and VitD supplementation may be useful in improving ICI treatment efficacy.

Indexed as

25-Hydroxyvitamin D3 1-alpha-HydroxylaseImmune Checkpoint InhibitorsHumansPolymorphism, Single NucleotideVitamin DVitamin D3 24-HydroxylaseVitamins25-Hydroxyvitamin D3 1-alpha-HydroxylaseImmune Checkpoint InhibitorsVitamin DVitamin D3 24-HydroxylaseVitaminsanti-PD-1 inhibitorsimmune checkpoint inhibitorsimmune-related adverse effectspolymorphismvitamin D

Identifiers

PMID36172344
PMCPMC9510606
OpenAlexW4296528597

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.