Evidence map›Paper›PMID 32992757›Full record

ArticleChildren (Basel, Switzerland)2020

Genetic and Environmental Risk Factors for Isolated Hemangiomas in Infants.

Anna Materna-Kiryluk, Katarzyna Wiśniewska, Barbara Więckowska, Katarzyna Wróblewska-Seniuk, Beata Jaroszewska-Świątek, Ewa Helwich, Anna Latos-Bieleńska

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 10 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

7 authors at 2 institutions in 1 country.

Anna Materna-KirylukPolish Registry of Congenital Malformations, Chair and Department of Medical Genetics, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-2889-5892
Katarzyna WiśniewskaDepartment of Preventive Medicine, Epidemiology Unit, Poznan University of Medical Sciences, 61-701 Poznan, Poland.
Barbara WięckowskaDepartment of Computer Science and Statistics, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-1811-2583
Katarzyna Wróblewska-SeniukDepartment of Newborns' Infectious Diseases, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0003-3908-6617
Beata Jaroszewska-ŚwiątekDepartment of Clinical Pediatrics, University of Warmia and Mazury in Olsztyn, Children's Hospital in Olsztyn, 10-651 Olsztyn, Poland.
Ewa HelwichDeparment of Neonatology and Neonatal Intensive Care, Institute of Mother and Child, 01-211 Warszawa, Poland.
Anna Latos-BieleńskaPolish Registry of Congenital Malformations, Chair and Department of Medical Genetics, Poznan University of Medical Sciences, 61-701 Poznan, Poland.
Poznan University of Medical Sciences · PLUniversity of Warmia and Mazury in Olsztyn · PL

Funding

The National Centre for Health Information Systems CSIOZ/172/2019
6 · The paper itself

Abstract

The goal of this analysis is to identify risk factors for infantile hemangiomas (IH) to better delineate hemangioma predisposition. We analyzed live birth children with isolated cutaneous hemangioma that were reported to the Polish Registry of Congenital Malformations from across Poland between the years 1998 and 2016. Lower birthweight and gestational age were the most significant risk factors associated with IH. We also observed a trend for a higher risk of IH with a lower level of maternal and paternal education. Moreover, mothers with IH have a higher probability of having a child with IH compared to fathers. However, this association is only present when the child is female. Similarly, a higher risk of hemangioma in a female child is found among mothers having relatives of the first degree with IH, compared to fathers with a similar pedigree. Our results suggest the role of exogenous factors in the etiology of IH. The analysis of familial cases suggests a multifactorial model of inheritance. The study indicates that female gender is an important risk factor for the expression of familial IH. Potential interaction of genetic risk factors with exposure to female sex hormones may play a role in the development of IH.

Indexed as

hereditary predispositioninfant hemangiomasrisk factorsvascular malformations

Identifiers

PMID32992757
PMCPMC7600327
OpenAlexW3088350520

What OpenQuestion holds

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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 OpenQuestion graph.