Cancer Risk by Attained Age among Children with Birth Defects in Arkansas

Jenil Patel1, Jeremy M Schraw2, Philip J Lupo2

  • 1Department of Epidemiology, Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, AR USA; Arkansas Center for Birth Defects Research and Prevention, Fay W. Boozman College of PublicHealth, University of Arkansas for Medical Science, Little Rock, AR USA.

Cancer Epidemiology
|August 23, 2020
PubMed

Insights

Children with birth defects, particularly cardiovascular and genitourinary, face the highest risk of pediatric cancer in their first year of life. This highlights the need for targeted surveillance strategies for early detection.

Area of Science:

  • Pediatric Oncology
  • Birth Defect Research
  • Epidemiology

Background:

  • Limited research exists on the association between birth defects and pediatric cancer risk across different ages.
  • Understanding these associations is crucial for early detection and intervention.

Purpose of the Study:

  • To assess pediatric cancer risk in children with and without birth defects, stratified by age at diagnosis.
  • To investigate specific birth defect types and their correlation with cancer risk.

Main Methods:

  • A cohort study linked data from Arkansas birth records, cancer registries, and birth defect monitoring systems (1996-2011).
  • Cox proportional hazards models were used to analyze cancer risk by attained age groups (<1, 1-4, 5-9, 10-14 years).
  • Associations were examined between various birth defect categories (any, chromosomal, non-chromosomal) and cancer subtypes.

Main Results:

  • The study included 629,086 children, with 3.7% having birth defects and 0.2% diagnosed with cancer.
  • Children with non-chromosomal birth defects (cardiovascular, genitourinary) had the highest cancer risk in the first year of life (HR 18.5).
  • Children with chromosomal birth defects showed increased cancer risk between 1-4 years old (HR 20.0).

Conclusions:

  • Pediatric cancer risk is elevated in children with birth defects, especially those under five years old.
  • Findings support the need for enhanced surveillance strategies for infants and young children with birth defects.
  • Early identification and monitoring can improve outcomes for children with congenital anomalies and cancer.
Abstract

Related Concept Videos

Cancer Prevention02:59

Cancer Prevention

Several factors can increase the risk of cancer in an individual. About 50% of cancer cases can be prevented by adopting a healthy lifestyle, regular exercise, eating healthy, and following a modest cancer prevention diet. Epidemiological studies have consistently shown that populations with vegetable and fruit-rich diets have reduced the incidence of cancer. On the other hand, populations who have a diet rich in animal fat, red meat, junk food, or high calories are predisposed to cancer.
Some...
7.5K
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.5K
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
3.8K
Nondisjunction01:21

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold...
4.6K
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
14.3K
Probability Laws01:49

Probability Laws

Overview
43.5K