Evidence map›Paper›PMID 31844428›Full record

ArticleOpen access Macedonian journal of medical sciences2019

Association of Gene Polymorphism of

Mustarim Mustarim, Yanwirasti Yanwirasti, Jamsari Jamsari, Rukmono Rukmono, Ricvan Dana Nindrea

Open access · diamondAbstract read
In one paragraph

Article in Open access Macedonian journal of medical sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. [Recent research on gene polymorphisms and genetic susceptibility of neonatal sepsis].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2024
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  4. Review
  5. Article
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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

5 authors at 2 institutions in 1 country.

Mustarim MustarimDoctoral of Biomedical Science, Faculty of Medicine, Universitas Andalas, Padang City, West Sumatera Province, Indonesia.
Yanwirasti YanwirastiDoctoral of Biomedical Science, Faculty of Medicine, Universitas Andalas, Padang City, West Sumatera Province, Indonesia.
Jamsari JamsariFaculty of Agriculture, Universitas Andalas, Padang City, West Sumatera Province, Indonesia.
Rukmono RukmonoFaculty of Medicine, Lampung University, Lampung, Indonesia.
Ricvan Dana NindreaDepartment of Public Health and Community Medicine, Faculty of Medicine, Universitas Andalas, Padang City, West Sumatera Province, Indonesia.
Andalas University · IDLampung University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeonatal sepsis is a health problem because it causes serious morbidity and mortality in neonate intensive care units. The susceptibility of neonates occurs due to the immaturity of immune system development as well as due to maternal and environmental risk factors that can cause infection. Identification of genetic variation in genes involved in the inflammatory process can help clarify the pathophysiology of sepsis in high-risk patients, useful for the development of new diagnostic tools, and specific management plans for more accurate predictions of patient's prognosis.

aimThis study aims to determine the association between gene polymorphism of

methodsCross-sectional observational studies with genomic DNA samples from infants with sepsis and non-sepsis which were stored according to the standard storage of genetic materials in the Biomedical Laboratory of Faculty of Medicine Universitas Andalas Padang City, Indonesia. This study is part of a previous study by Rukmono P. Continued with PCR examination, sequencing and bioinformatics analysis.

resultsOnly

conclusionGene polymorphism of

Indexed as

BPICD14IL1βMMP16Neonatal sepsisPolymorphismSingle nucleotide polymorphism

Identifiers

PMID31844428
PMCPMC6901854
OpenAlexW2981881665

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.