Congenital abnormalities and hepatoblastoma: A report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB)

Rajkumar Venkatramani, Logan G. Spector, Michael Georgieff, Gail Tomlinson, Mark Krailo, Marcio Malogolowkin, Wendy Kohlmann, Karen Curtin, Rachel K. Fonstad, Joshua D. Schiffman

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Beckwith-Wiedemann Syndrome (BWS) and familial adenomatous polyposis (FAP) are known to predispose to hepatoblastoma (HB). A case-control study was conducted through the Children's Oncology Group (COG) to study the association of HB with isolated congenital abnormalities. Cases (N=383) were diagnosed between 2000 and 2008. Controls (N=387) were recruited from state birth registries, frequency matched for sex, region, year of birth, and birth weight. Data on congenital abnormalities among subjects and covariates were obtained by maternal telephone interview. Odds ratios (OR) and 95% confidence intervals (CI) describing the association between congenital abnormalities with HB, adjusted for sex, birth weight, maternal age and maternal education, were calculated using unconditional logistic regression. There was a significant association of HB with kidney, bladder, or sex organ abnormalities (OR=4.75; 95% CI: 1.74-13) which appeared to be specific to kidney/bladder defects (OR=4.3; 95% CI: 1.2-15.3) but not those of sex organs (OR=1.24; 95% CI: 0.37-4.1). Elevated but non-significant ORs were found for spina bifida or other spinal defects (OR=2.12; 95% CI: 0.39-11.7), large or multiple birthmarks (OR=1.33; 95% CI: 0.81-2.21). The results were validated through the Utah Population Database (UPDB), a statewide population-based registry linking birth certificates, medical records, and cancer diagnoses. In the UPDB, there were 29 cases and 290 population controls matched 10:1 on sex and birth year. Consistent with the COG findings, kidney/bladder defects were associated with hepatoblastoma. These results confirm the association of HB with kidney/bladder abnormalities.

Original languageEnglish (US)
Pages (from-to)2250-2255
Number of pages6
JournalAmerican Journal of Medical Genetics, Part A
Volume164
Issue number9
DOIs
StatePublished - Jan 1 2014
Externally publishedYes

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Hepatoblastoma
Population Groups
Odds Ratio
Databases
Confidence Intervals
Urinary Bladder
Kidney
Parturition
Birth Weight
Registries
Mothers
Beckwith-Wiedemann Syndrome
Population
Birth Certificates
Spinal Dysraphism
Adenomatous Polyposis Coli
Population Control
Maternal Age
Medical Records
Case-Control Studies

Keywords

  • Beckwith-Wiedemann syndrome
  • Case-control study
  • Congenital abnormality
  • Congenital anomaly
  • Familial adenomatous polyposis
  • Hepatoblastoma
  • Kidney abnormalities

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Congenital abnormalities and hepatoblastoma : A report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB). / Venkatramani, Rajkumar; Spector, Logan G.; Georgieff, Michael; Tomlinson, Gail; Krailo, Mark; Malogolowkin, Marcio; Kohlmann, Wendy; Curtin, Karen; Fonstad, Rachel K.; Schiffman, Joshua D.

In: American Journal of Medical Genetics, Part A, Vol. 164, No. 9, 01.01.2014, p. 2250-2255.

Research output: Contribution to journalArticle

Venkatramani, R, Spector, LG, Georgieff, M, Tomlinson, G, Krailo, M, Malogolowkin, M, Kohlmann, W, Curtin, K, Fonstad, RK & Schiffman, JD 2014, 'Congenital abnormalities and hepatoblastoma: A report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB)', American Journal of Medical Genetics, Part A, vol. 164, no. 9, pp. 2250-2255. https://doi.org/10.1002/ajmg.a.36638
Venkatramani, Rajkumar ; Spector, Logan G. ; Georgieff, Michael ; Tomlinson, Gail ; Krailo, Mark ; Malogolowkin, Marcio ; Kohlmann, Wendy ; Curtin, Karen ; Fonstad, Rachel K. ; Schiffman, Joshua D. / Congenital abnormalities and hepatoblastoma : A report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB). In: American Journal of Medical Genetics, Part A. 2014 ; Vol. 164, No. 9. pp. 2250-2255.
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