Evidence map›Paper›PMID 29085969›Full record

Trial reportUrolithiasis2018

Etiologic risk factors and vitamin D receptor gene polymorphisms in under one-year-old infants with urolithiasis.

Ezgi Yangın Ergon, İpek Ozunan Akil, Fatma Taneli, Arzu Oran, Beyhan Cengız Ozyurt

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Urolithiasis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 3 pooled it
0.7field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 3 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Relationship Between theFrontiers in genetics · 2020
    Pooled it
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
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 1 institution in 1 country.

Ezgi Yangın ErgonDepartment of Pediatrics, Celal Bayar University, Manisa, Turkey. yanginezgi@yahoo.com.ORCID http://orcid.org/0000-0003-0836-7379
İpek Ozunan AkilDepartment of Pediatric Nephrology, Celal Bayar University, Manisa, Turkey.
Fatma TaneliDepartment of Medical Chemistry, Celal Bayar University, Manisa, Turkey.
Arzu OranDepartment of Medical Chemistry, Celal Bayar University, Manisa, Turkey.
Beyhan Cengız OzyurtDepartment of Public Health, Celal Bayar University, Manisa, Turkey.
Manisa Celal Bayar University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of urinary tract stones in infancy has been increasing in Turkey. Risk factors and vitamin D receptor (VDR) gene polymorphisms were investigated in infants aged < 1 year who had stones. Forty infants with urinary tract stones and 80 infants without stones, aged < 1 year were enrolled in this study. Detailed surveys were taken of all infants, metabolic parameters and ApaI and FokI VDR gene polymorphisms were investigated. Infants with stones tended to be more commonly fed formula and multivitamins (vitamins A, C, D) (p < 0.05). Positive family history came into prominence in the stony group (p < 0.05). There were no significant differences in ApaI and FokI VDR gene polymorphisms between the groups with stones and the control groups. However, CA genotype of ApaI polymorphism was associated with family history and C allele of ApaI was related with family history and hypercalciuria (p < 0.05). Hypercalciuria emerged as an underlying metabolic abnormality in the etiology of stones, and was observed at a rate of 38%. Infants who are given formula and multivitamins for vitamin D supplementation are at increased risk for the formation of urinary tract stones. VDR gene polymorphisms cause the formation of urinary tract stones and affect calcium (Ca) metabolism.

Indexed as

Dietary SupplementsGenetic Predisposition to DiseaseHypercalciuriaReceptors, CalcitriolUrolithiasisVitamin DCalciumCase-Control StudiesDiet SurveysFemaleGene FrequencyHumansIncidenceInfantInfant FormulaInfant, NewbornCalciumReceptors, CalcitriolVDR protein, humanVitamin DInfantMetabolic risk factorUrolithiasisVDR gene polymorphismVitamin D

Identifiers

PMID29085969
OpenAlexW2766187835

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.