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Insulin and glucose homeostasis in childhood cancer survivors treated with abdominal radiation: A pilot study.
Friedman, Danielle Novetsky; Hilden, Patrick; Moskowitz, Chaya S; Wolden, Suzanne L; Tonorezos, Emily S; Antal, Zoltan; Carlow, Dean; Modak, Shakeel; Cheung, Nai-Kong; Oeffinger, Kevin C; Sklar, Charles A.
Afiliación
  • Friedman DN; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Hilden P; Weill Cornell Medical College, New York, NY.
  • Moskowitz CS; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Wolden SL; Weill Cornell Medical College, New York, NY.
  • Tonorezos ES; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Antal Z; Weill Cornell Medical College, New York, NY.
  • Carlow D; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Modak S; Weill Cornell Medical College, New York, NY.
  • Cheung NK; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Oeffinger KC; Weill Cornell Medical College, New York, NY.
  • Sklar CA; Memorial Sloan Kettering Cancer Center, New York, NY.
Pediatr Blood Cancer ; 65(11): e27304, 2018 11.
Article en En | MEDLINE | ID: mdl-30009519
ABSTRACT

BACKGROUND:

Childhood cancer survivors exposed to abdominal radiation (abdRT) are at increased risk for both insulin-dependent and non-insulin-dependent diabetes. We sought to clarify the pathophysiology of diabetes after abdRT by performing dynamic studies of insulin and glucose and testing for type 1 diabetes-associated autoantibodies. PROCEDURE Cross-sectional analysis of 2-year childhood cancer survivors treated with abdRT at age ≤21 years who underwent oral glucose tolerance testing and assessment of diabetes-related autoantibodies from December 2014 to September 2016. Prevalence of insulin/glucose derangements, indices of insulin sensitivity/secretion (homeostatic model assessment of insulin resistance [HOMA-IR], whole-body insulin sensitivity, insulinogenic index), autoantibody positivity, and treatment/demographic factors associated with adverse metabolic outcomes were assessed.

RESULTS:

Among 40 participants previously exposed to abdRT (57.5% male; median age at cancer diagnosis, 3.3 years [range, 0.5-20.1]; median age at study 14.3 years [range, 8.3-49.8]; none with obesity), 9 (22.5%) had glucose derangements (n = 4 with impaired fasting glucose [≥100 mg/dL]; n = 4 with impaired glucose tolerance [2-hour glucose 140-199 mg/dL]; n = 1 with previously unrecognized diabetes [2-hour glucose ≥200 mg/dL]). Three of the four individuals with impaired fasting glucose also had insulin resistance, as measured by HOMA-IR; an additional four subjects with normal glucose tolerance were insulin resistant. The subject with diabetes had normal HOMA-IR. No participant had absolute insulinopenia or >1 positive diabetes-related autoantibody.

CONCLUSIONS:

This study suggests that radiation-induced damage to the insulin-producing ß-cells is an unlikely explanation for the early derangements in glucose metabolism observed after abdRT. Research into alternative pathways leading to diabetes after abdRT is needed.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Traumatismos por Radiación / Radioterapia / Glucemia / Supervivientes de Cáncer / Insulina Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Traumatismos por Radiación / Radioterapia / Glucemia / Supervivientes de Cáncer / Insulina Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2018 Tipo del documento: Article