From the Department of Molecular Medicine and Surgery, Center for Molecular Medicine (C.M.G., G.T., F.T., A.S.N., A.N.), Unit of Epidemiology, Institute of Environmental Medicine (G.T.), and Department of Women's and Children's Health (T.S.), Karolinska Institutet; Department of Clinical Genetics and Genomics (F.T., A.N.), Department of Radiology (A.S.N.), and Department of Child Neurology, Astrid Lindgren Children's Hospital (T.S.), Karolinska University Hospital, Stockholm; Department of Clinical Genetics and Genomics (A.N.), Sahlgrenska University Hospital, Gothenburg; and Institute of Biomedicine, Department of Laboratory Medicine (A.N.), University of Gothenburg, Sweden.
Neurology. 2024 Oct 22;103(8):e209883. doi: 10.1212/WNL.0000000000209883. Epub 2024 Sep 19.
Muscular dystrophies and myotonic disorders are genetic disorders characterized by progressive skeletal muscle degeneration and weakness. Epidemiologic studies have found an increased cancer risk in myotonic dystrophy, although the cancer risk spectrum is poorly characterized. In patients with muscular dystrophy, the cancer risk is uncertain. We aimed to determine the overall cancer risk and cancer risk spectrum in patients with muscular dystrophy and myotonic dystrophy using data from the Swedish National registers.
We performed a matched cohort study in all patients with muscular dystrophy or myotonic dystrophy born in Sweden 1950-2017 and 50 matched comparisons by sex, year of birth, and birth county per individual. The association with cancer overall and specific malignancies was estimated using stratified Cox proportional hazard models.
We identified 2,355 and 1,968 individuals with muscular dystrophy and myotonic dystrophy, respectively. No increased overall cancer risk was found in muscular dystrophy. However, we observed an increased risk of astrocytomas and other gliomas during childhood (hazard ratio [HR] 8.70, 95% CI 3.57-21.20) and nonthyroid endocrine cancer (HR 2.35, 95% CI 1.03-5.34) and pancreatic cancer (HR 4.33, 95% CI 1.55-12.11) in adulthood. In myotonic dystrophy, we found an increased risk of pediatric brain tumors (HR 3.23, 95% CI 1.16-9.01) and an increased overall cancer risk in adults (HR 2.26, CI 1.92.2.66), specifically brain tumors (HR 10.44, 95% CI 7.30-14.95), thyroid (HR 3.92, 95% CI 1.70-9.03), and nonthyroid endocrine cancer (HR 7.49, 95% CI 4.47-12.56), endometrial (HR 8.32, 95% CI 4.22-16.40), ovarian (HR 4.00, 95% CI 1.60-10.01), and nonmelanoma skin cancer (HR 3.27, 95% CI 1.32-8.13).
Here, we analyze the cancer risk spectrum of patients with muscular dystrophy and myotonic dystrophy. To the best of our knowledge, this is the first report of an increased risk for CNS tumors in childhood and adult nonthyroid endocrine and pancreatic cancer in muscular dystrophy. Furthermore, for myotonic dystrophy, we confirmed previously reported associations with cancer and expanded the cancer spectrum, finding an unreported increased risk for nonthyroid endocrine cancer. Additional studies confirming the cancer risk and delineating the cancer spectrum in different genetic subtypes of muscular dystrophies are warranted before considering altered cancer screening recommendations than for the general population.
肌营养不良症和强直性肌营养不良症是具有进行性骨骼肌退化和无力特征的遗传疾病。流行病学研究发现强直性肌营养不良患者癌症风险增加,尽管癌症风险谱描述不佳。在肌营养不良症患者中,癌症风险不确定。我们旨在使用瑞典国家登记处的数据,确定肌营养不良症和强直性肌营养不良症患者的总体癌症风险和癌症风险谱。
我们对 1950 年至 2017 年在瑞典出生的所有肌营养不良症或强直性肌营养不良症患者进行了匹配队列研究,并按性别、出生年份和每个个体的出生县对 50 个匹配对照进行了研究。使用分层 Cox 比例风险模型估计总体癌症和特定恶性肿瘤的关联。
我们确定了 2355 名肌营养不良症患者和 1968 名强直性肌营养不良症患者。肌营养不良症患者的总体癌症风险没有增加。然而,我们观察到儿童时期星形细胞瘤和其他神经胶质瘤(危险比 [HR] 8.70,95%CI 3.57-21.20)、非甲状腺内分泌癌(HR 2.35,95%CI 1.03-5.34)和胰腺癌(HR 4.33,95%CI 1.55-12.11)的风险增加,以及成年期的胰腺癌症。在强直性肌营养不良症中,我们发现儿童期脑肿瘤(HR 3.23,95%CI 1.16-9.01)和成年期总体癌症风险增加(HR 2.26,CI 1.92.2.66),特别是脑肿瘤(HR 10.44,95%CI 7.30-14.95)、甲状腺(HR 3.92,95%CI 1.70-9.03)和非甲状腺内分泌癌(HR 7.49,95%CI 4.47-12.56)、子宫内膜癌(HR 8.32,95%CI 4.22-16.40)、卵巢癌(HR 4.00,95%CI 1.60-10.01)和非黑色素瘤皮肤癌(HR 3.27,95%CI 1.32-8.13)。
在这里,我们分析了肌营养不良症和强直性肌营养不良症患者的癌症风险谱。据我们所知,这是首次报告儿童时期中枢神经系统肿瘤和成年非甲状腺内分泌和胰腺癌风险增加的报告。此外,对于强直性肌营养不良症,我们证实了先前报道的与癌症的关联,并扩展了癌症谱,发现了以前未报告的非甲状腺内分泌癌风险增加。在考虑改变癌症筛查建议以适应一般人群之前,需要进一步研究以确认癌症风险并描绘不同肌营养不良症遗传亚型的癌症谱。