Benign and malignant tumors in the UK myotonic dystrophy patient registry

Muscle Nerve. 2018 Feb;57(2):316-320. doi: 10.1002/mus.25736. Epub 2017 Jul 24.

Abstract

Introduction: In light of recent evidence indicating that cancer is part of the myotonic dystrophy (DM) phenotype, we assessed the prevalence of benign and malignant tumors among 220 patients enrolled in the UK Myotonic Dystrophy Patient Registry and evaluated factors associated with their development.

Methods: A survey was distributed to collect tumor history and lifestyle information. We used multinomial logistic regression for the analysis.

Results: Thirty-nine benign (30 patients), and 16 malignant (15 patients) tumors were reported. Increasing age (odds ratio [OR] = 1.13, 95% confidence interval [CI] = 1.05-1.21, P = 0.001) and earlier age at DM diagnosis (OR = 1.06, 95% CI = 1.00-1.13, P = 0.04) were associated with benign and malignant tumors (OR = 1.20, 95% CI = 1.10-1.30, P < 0.001 and OR = 1.08, 95% CI = 1.01-1.15, P = 0.02, respectively). Female gender was associated with benign tumors only (OR = 6.43, 95% CI = 1.79-23.04, P = 0.004). No associations were observed between tumors and smoking (P = 0.24), alcohol consumption (P = 0.50), or body mass index (P = 0.21).

Discussion: Our results confirm previous findings suggesting a limited role for common lifestyle factors and a potential genetic contribution in DM tumor predisposition. Muscle Nerve 57: 316-320, 2018.

Keywords: cancer; lifestyle factors; myotonic dystrophy; risk factors; smoking; tumor.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Age Factors
  • Age of Onset
  • Aged
  • Female
  • Humans
  • Life Style
  • Male
  • Middle Aged
  • Myotonic Dystrophy / complications*
  • Myotonic Dystrophy / epidemiology*
  • Neoplasms / complications*
  • Neoplasms / epidemiology*
  • Registries
  • Risk Factors
  • Sex Factors
  • United Kingdom / epidemiology