Evidence map›Paper›PMID 34539750›Full record

ArticleFrontiers in genetics2021

A Functional Variant of CXCL16 Is Associated With Predisposition to Sepsis and MODS in Trauma Patients: Genetic Association Studies.

Jianhui Sun, Huacai Zhang, Di Liu, Li Cui, Qiang Wang, Lebin Gan, Dalin Wen, Jun Wang, Juan Du, Hong Huang and 4 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01713205 (Identifying Severe Trauma Patients at High Risk of Post-traumatic Complications), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 35% 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.

NCT01713205 unknown statusnot on this map

Identifying Severe Trauma Patients at High Risk of Post-traumatic Complications

TypeobservationalSponsorJiang JianxinRan2012 to 2023Enrolled3,500ConditionsTrauma, Sepsis, Multiple Organ Dysfunction Syndrome
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 5 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

14 authors at 4 institutions in 1 country.

Jianhui SunDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Huacai ZhangDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Di LiuDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Li CuiDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Qiang WangDepartment of Emergency, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Lebin GanDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Dalin WenDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Jun WangDepartment of Emergency, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Juan DuDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Hong HuangDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Anqiang ZhangDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Jin DengDepartment of Emergency, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Jianxin JiangDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Ling ZengDepartment of Trauma Medical Center, Daping Hospital, Army Medical University, Chongqing, China.
Army Medical University · CNDaping Hospital · CNGuiyang Medical University · CNAffiliated Hospital of Guizhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCXC chemokines are mediators which mediate immune cells migration to sites of inflammation and injury. Chemokine C-X-C motif ligand 16 (CXCL16) plays an important role in the occurrence and development of sepsis through leukocyte chemotaxis, leukocyte adhesion and endotoxin clearance. In this study, we selected a set of tagging single nucleotide polymorphisms (tag SNPs) in the CXCL16 gene and investigated their clinical relevance to the development of sepsis and multiple organ dysfunction syndrome (MODS) in patients with major trauma in three independent Chinese Han populations.

methodsA total of 1,620 major trauma patients were enrolled in this study. Among these patients, 920 came from Chongqing in western China, 350 came from Zhejiang Province in eastern China, and 350 came from Guizhou Province in southwestern China. The improved multiplex ligation detection reaction (iMLDR) method was employed in the genotyping and genetic association analyses to determine the associations between CXCL16 haplotypes and sepsis morbidity rate and higher MOD scores in three cohorts.

resultsOnly CXCL16 T123V181 haplotype was associated with an increased risk for sepsis morbidity and higher MOD scores in the three cohorts (OR = 1.89,

conclusionWe demonstrate the mechanism of CXCL16 T123V181 haplotype which regulates the sepsis morbidity rate and thus provide a new biomarker for early diagnosis of sepsis and MODS. CLINICAL

trial registrationwww.ClinicalTrials.gov, identifier NCT01713205 (https://www.clinicaltrials.gov/ct2/results?cond=&term=+NCT01713205&cntry=&state=&city=&dist=).

Indexed as

CXCL16multiple organ dysfunctionsepsissingle nucleotide polymorphismstrauma

Identifiers

PMID34539750
PMCPMC8446271
OpenAlexW3198819359

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Registered trials

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.