Aging-related disease risks among young thyroid cancer survivors

  • Brenna E. Blackburn
  • , Patricia A. Ganz
  • , Kerry Rowe
  • , John Snyder
  • , Yuan Wan
  • , Vikrant Deshmukh
  • , Michael Newman
  • , Alison Fraser
  • , Ken Smith
  • , Kimberly Herget
  • , Jaewhan Kim
  • , Anne C. Kirchhoff
  • , Christina Porucznik
  • , Heidi Hanson
  • , Marcus Monroe
  • , Mia Hashibe

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Background: Thyroid cancer is the most rapidly increasing cancer in the United States, affects a young population, has high survival, and is one of the most common cancers in people under age 40. The aim of this study was to examine the risks of aging-related diseases in a statewide sample of thyroid cancer survivors who were diagnosed <40 years compared with those diagnosed ≥40 and a cancer-free sample. Methods: Thyroid cancer survivors diagnosed 1997 to 2012 were matched to up to 5 cancer-free individuals on birth year, sex, birth state, using the statewide Utah Population Database. Medical records were used to identify disease diagnoses stratified over three time periods: 1 to 5, >5 to 10, and 10þ years after cancer diagnosis. Cox proportional hazards models were used to estimate hazard ratios with adjustment on matching factors, race, body mass index, and Charlson Comorbidity Index. Results: There were 3,706 thyroid cancer survivors and 15,587 matched cancer-free individuals (1,365 cases diagnosed <40 years old). Both age groups had increased risks for multiple circulatory health conditions 1 to 5 years after cancer diagnosis compared with cancer-free individuals. Survivors <40 had a higher risk of hypertension, cardiomyopathy, and nutritional deficiencies. Conclusions: Increased risks for diseases associated with aging were observed for both age groups, with younger thyroid cancer survivors having higher risks for select diseases. Impact: As thyroid cancer survivors in this study were found to have increased risks for aging-related diseases, future studies are needed to assess what can be done to reduce the increased risks of these long-term health effects.

Original languageEnglish
Pages (from-to)1695-1704
Number of pages10
JournalCancer Epidemiology Biomarkers and Prevention
Volume26
Issue number12
DOIs
StatePublished - Dec 1 2017
Externally publishedYes

Funding

This work was supported by grants from the National Cancer Institute (R03 CA 159357, R21 CA185811), the Huntsman Cancer Institute, Cancer Control and Population Sciences Program (HCI Cancer Center Support Gran-tP30CA042014), and the NCRR grant, "Sharing Statewide Health Data for Genetic Research" (R01 RR021746, G. Mineau, PI) with additional support from the Utah State Department of Health and the University of Utah. We thank the Pedigree and Population Resource of the Huntsman Cancer Institute, University of Utah (funded in part by the Huntsman Cancer Foundation) for its role in theongoingcollection,maintenance and support ofthe Utah Population Database. We thank the University of Utah Center for Clinical and Translational Science (funded by NIH Clinical and Translational Science Awards), the Pedigree and Population Resource, University of Utah Information Technology Services and Biomedical Informatics Core for establishing the Master Subject Index between the Utah Population Database, the University of Utah Health Sciences Center and Intermountain Healthcare. This work was supported by grants from the National Cancer Institute (R03 CA 159357, R21 CA185811), the Huntsman Cancer Institute, Cancer Control and Population Sciences Program (HCI Cancer Center Support Grant P30CA042014), and the NCRR grant, "Sharing Statewide Health Data for Genetic Research" (R01 RR021746, G. Mineau, PI) with additional support from the Utah State Department of Health and the University of Utah. We thank the Pedigree and Population Resource of the Huntsman Cancer Institute, University of Utah (funded in part by the Huntsman Cancer Foundation) for its role in the ongoing collection, maintenance and support of the Utah Population Database. We thank the University of Utah Center for Clinical and Translational Science (funded by NIH Clinical and Translational Science Awards), the Pedigree and Population Resource, University of Utah Information Technology Services and Biomedical Informatics Core for establishing the Master Subject Index between the Utah Population Database, the University of Utah Health Sciences Center and Intermountain Healthcare.

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