Evidence map›Paper›PMID 40626678›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2025

Cancer and benign tumors in myotonic dystrophy, facioscapulohumeral muscular dystrophy, and oculopharyngeal muscular dystrophy: a 23-year, single-center, retrospective study.

Naman Bareja, Brinda Desai, Michal Vytopil, Jayashri Srinivasan, Mehdi Ghasemi

Abstract read
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Naman BarejaDepartment of Neurology, Tufts Medical Center, Boston, MA, USA.
Brinda DesaiDepartment of Neurology, Lahey Hospital and Medical Center, Burlington, MA, USA.
Michal VytopilDepartment of Neurology, Lahey Hospital and Medical Center, Burlington, MA, USA.
Jayashri SrinivasanDepartment of Neurology, Lahey Hospital and Medical Center, Burlington, MA, USA.
Mehdi GhasemiDepartment of Neurology, Lahey Hospital and Medical Center, Burlington, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Some muscular dystrophies, such as myotonic dystrophy type 1 and 2 (DM1 and DM2), facioscapulohumeral muscular dystrophy (FSHD), and oculopharyngeal muscular dystrophy (OPMD), are caused by genetic mutations that may affect the expression and function of various cancer-related genes. We assessed the frequency and type of cancers and benign tumors in patients with DM1, DM2, FSHD, and OPMD. Methods: We conducted a single-center, retrospective, cross-sectional study on patients with DM1, DM2, FSHD, and OPMD at our institution from January 2000 to September 2023. Results: Seventy seven (46 female) DM1, 20 (15 female) DM2, 40 (18 female) FSHD, and 46 (22 female) OPMD patients were included, among which 22 (28.57%), 9 (45%), 7 (17.5%), and 15 (32.61%) patients had at least one cancer, respectively. Median age (range) of patients where presence or absence of cancer was ascertained was 65 (18-87), 63.5 (45-86), 61 (27-83), and 71.5 (40-82) years, respectively (P < 0.0001). Overall, non-sex-related cancers were more frequent than sex-related cancers among all patients together. Independent to sex and age, DM1 patients had an increased risk of non-sex-related cancers compared to non-DM cases. Melanoma (P < 0.01) and testicular (P < 0.05) cancers were significantly more frequent in DM2 and OMPD patients, respectively. DM patients had also increased risk of non-sex related benign tumors (including skin and thyroid benign tumors) compared to non-DM patients. Conclusions: Our study highlights the differences in the prevalence of cancers and benign tumors among patients with DM1, DM2, FSHD, and OPMD, underscoring the potential need for regular screening for specific cancers.

Indexed as

Muscular Dystrophy, FacioscapulohumeralMuscular Dystrophy, OculopharyngealMyotonic DystrophyNeoplasmsAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesYoung Adultcancerfacioscapulohumeral muscular dystrophy (FSHD)melanomaMyotonic dystrophyoculopharyngeal muscular dystrophy (OPMD)thyroid tumor

Identifiers

PMID40626678
PMCPMC12250585

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.