Literature DB >> 31105274

Estimating prevalence for limb-girdle muscular dystrophy based on public sequencing databases.

Sander Pajusalu1,2,3, Nicole J Lake1,4, Wei Liu5, Geyu Zhou5, Nilah Ioannidis6,7, Plavi Mittal6,8, Nicholas E Johnson9, Conrad C Weihl10, Bradley A Williams6, Douglas E Albrecht6, Laura E Rufibach6, Monkol Lek11.   

Abstract

PURPOSE: Limb-girdle muscular dystrophies (LGMD) are a genetically heterogeneous category of autosomal inherited muscle diseases. Many genes causing LGMD have been identified, and clinical trials are beginning for treatment of some genetic subtypes. However, even with the gene-level mechanisms known, it is still difficult to get a robust and generalizable prevalence estimation for each subtype due to the limited amount of epidemiology data and the low incidence of LGMDs.
METHODS: Taking advantage of recently published exome and genome sequencing data from the general population, we used a Bayesian method to develop a robust disease prevalence estimator.
RESULTS: This method was applied to nine recessive LGMD subtypes. The estimated disease prevalence calculated by this method was largely comparable with published estimates from epidemiological studies; however, it highlighted instances of possible underdiagnosis for LGMD2B and 2L.
CONCLUSION: The increasing size of aggregated population variant databases will allow for robust and reproducible prevalence estimates of recessive disease, which is critical for the strategic design and prioritization of clinical trials.

Entities:  

Keywords:  disease prevalence; limb-girdle muscular dystrophy; rare disease

Mesh:

Year:  2019        PMID: 31105274     DOI: 10.1038/s41436-019-0544-8

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  14 in total

1.  Genetic Profile of Patients with Limb-Girdle Muscle Weakness in the Chilean Population.

Authors:  Mathieu Cerino; Patricio González-Hormazábal; Mario Abaji; Sebastien Courrier; Francesca Puppo; Yves Mathieu; Alejandra Trangulao; Nicholas Earle; Claudia Castiglioni; Jorge Díaz; Mario Campero; Ricardo Hughes; Carmen Vargas; Rocío Cortés; Karin Kleinsteuber; Ignacio Acosta; J Andoni Urtizberea; Nicolas Lévy; Marc Bartoli; Martin Krahn; Lilian Jara; Pablo Caviedes; Svetlana Gorokhova; Jorge A Bevilacqua
Journal:  Genes (Basel)       Date:  2022-06-16       Impact factor: 4.141

2.  Comprehensive analysis of ADA2 genetic variants and estimation of carrier frequency driven by a function-based approach.

Authors:  Hyuk Jee; Zhengping Huang; Samantha Baxter; Yuelong Huang; Maria L Taylor; Lauren A Henderson; Sofia Rosenzweig; Aman Sharma; Eugene P Chambers; Michael S Hershfield; Qing Zhou; Fatma Dedeoglu; Ivona Aksentijevich; Peter A Nigrovic; Anne O'Donnell-Luria; Pui Y Lee
Journal:  J Allergy Clin Immunol       Date:  2021-05-15       Impact factor: 10.793

3.  Duchenne muscular dystrophy-like phenotype in an LGMD2I patient with novel FKRP gene variants.

Authors:  Tetsuya Okazaki; Kaori Matsuura; Noriko Kasagi; Kaori Adachi; Masachika Kai; Mariko Okubo; Ichizo Nishino; Eiji Nanba; Yoshihiro Maegaki
Journal:  Hum Genome Var       Date:  2020-04-20

4.  Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect.

Authors:  Marzieh Mojbafan; Reza Bahmani; Samira Dabbagh Bagheri; Zohreh Sharifi; Sirous Zeinali
Journal:  Orphanet J Rare Dis       Date:  2020-01-14       Impact factor: 4.123

5.  The prevalence of hereditary neuromuscular disorders in Northern Norway.

Authors:  Kai Ivar Müller; Marijke Van Ghelue; Irene Lund; Christoffer Jonsrud; Kjell Arne Arntzen
Journal:  Brain Behav       Date:  2020-11-13       Impact factor: 2.708

6.  The global carrier frequency and genetic prevalence of Upshaw-Schulman syndrome.

Authors:  Ting Zhao; Shanghua Fan; Liu Sun
Journal:  BMC Genom Data       Date:  2021-11-17

Review 7.  A Journey with LGMD: From Protein Abnormalities to Patient Impact.

Authors:  Dimitra G Georganopoulou; Vasilis G Moisiadis; Firhan A Malik; Ali Mohajer; Tanya M Dashevsky; Shirley T Wuu; Chih-Kao Hu
Journal:  Protein J       Date:  2021-06-10       Impact factor: 2.371

8.  A Small-Molecule Approach to Restore a Slow-Oxidative Phenotype and Defective CaMKIIβ Signaling in Limb Girdle Muscular Dystrophy.

Authors:  Jian Liu; Jesus Campagna; Varghese John; Robert Damoiseaux; Ekaterina Mokhonova; Diana Becerra; Huan Meng; Elizabeth M McNally; April D Pyle; Irina Kramerova; Melissa J Spencer
Journal:  Cell Rep Med       Date:  2020-10-20

9.  Base editing repairs an SGCA mutation in human primary muscle stem cells.

Authors:  Helena Escobar; Anne Krause; Sandra Keiper; Janine Kieshauer; Stefanie Müthel; Manuel García de Paredes; Eric Metzler; Ralf Kühn; Florian Heyd; Simone Spuler
Journal:  JCI Insight       Date:  2021-05-24

10.  Case report: 'AARS2 leukodystrophy'.

Authors:  Tobias Melton Axelsen; Tzvetelina Lubenova Vammen; Mads Bak; Nelsan Pourhadi; Christian Midtgaard Stenør; Sabine Grønborg
Journal:  Mol Genet Metab Rep       Date:  2021-07-13
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