Maternal and perinatal factors are associated with risk of pediatric central nervous system tumors and poorer survival after diagnosis.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
17 05 2021
Historique:
received: 20 10 2020
accepted: 06 04 2021
entrez: 18 5 2021
pubmed: 19 5 2021
medline: 3 11 2021
Statut: epublish

Résumé

Central nervous system (CNS) tumors are the most common solid tumors in children. Findings on the role of maternal and perinatal factors on the susceptibility or outcome of these tumors are inconclusive. Therefore, we investigated the association between these early-life factors, risk, and survival of pediatric CNS tumors, using data from one of the world's largest and most diverse cancer registries. Information on pediatric CNS tumor cases (n = 1950) for the period 1995-2011 was obtained from the Texas Cancer Registry. Birth certificate controls were frequency-matched on birth year at a ratio of 10:1 for the same period. Evaluated maternal and perinatal variables were obtained from birth records. Unconditional logistic regression was used to generate adjusted odds ratios (ORs) and 95% confidence intervals (CIs) for etiological factors. Additionally, Cox proportional hazards regression was employed to assess adjusted hazard ratios (HRs) and 95% CIs for survival factors. The results indicated that Hispanic and non-Hispanic black mothers were less likely to have children with CNS tumors compared to non-Hispanic white mothers (OR 0.88 [95% CI 0.78-0.98] P-value = 0.019; OR 0.79 [95% CI 0.67-0.93 P-value = 0.004], respectively). Infants born large for gestational age (OR 1.26 [95% CI 1.07-1.47] P-value = 0.004) and those delivered pre-term (OR 1.19 [95% CI 1.04-1.38] P-value = 0.013) showed an increased risk of CNS tumors. Infants born by vaginal forceps or vacuum delivery had a higher risk of CNS tumors compared to those born by spontaneous vaginal delivery (OR 1.35 [95% CI 1.12-1.62] P-value = 0.002). Additionally, offspring of Hispanic and non-Hispanic black mothers showed a higher risk of death (HR 1.45 [95% CI 1.16-1.80] P-value = 0.001; HR 1.53 [95% CI 1.12-2.09] P-value = 0.008, respectively). Infants born by cesarean had a higher risk of death compared to those delivered vaginally (HR 1.28 [95% CI 1.05-1.57] P-value = 0.016). These findings indicate the important role of maternal and perinatal characteristics in the etiology and survival of these clinically significant malignancies.

Identifiants

pubmed: 34001927
doi: 10.1038/s41598-021-88385-3
pii: 10.1038/s41598-021-88385-3
pmc: PMC8129132
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

10410

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Auteurs

Maral Adel Fahmideh (M)

Department of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, TX, USA. Maral.Adel@bcm.edu.
Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA. Maral.Adel@bcm.edu.
Department of Pediatrics, Center for Epidemiology and Population Health, Baylor College of Medicine, Houston, TX, USA. Maral.Adel@bcm.edu.

Erin C Peckham-Gregory (EC)

Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Department of Pediatrics, Center for Epidemiology and Population Health, Baylor College of Medicine, Houston, TX, USA.
Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

Jeremy M Schraw (JM)

Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Department of Pediatrics, Center for Epidemiology and Population Health, Baylor College of Medicine, Houston, TX, USA.
Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

Murali Chintagumpala (M)

Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Cancer Center, Texas Children's Hospital, Houston, TX, USA.

Stephen C Mack (SC)

Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Cancer Center, Texas Children's Hospital, Houston, TX, USA.

Philip J Lupo (PJ)

Department of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, TX, USA.
Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Department of Pediatrics, Center for Epidemiology and Population Health, Baylor College of Medicine, Houston, TX, USA.
Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Cancer Center, Texas Children's Hospital, Houston, TX, USA.

Michael E Scheurer (ME)

Department of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, TX, USA.
Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Department of Pediatrics, Center for Epidemiology and Population Health, Baylor College of Medicine, Houston, TX, USA.
Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Cancer Center, Texas Children's Hospital, Houston, TX, USA.

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