Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Nov;10(11):2074-2091.
doi: 10.1002/acn3.51895. Epub 2023 Sep 10.

Evidence-based consensus guidelines for ALS genetic testing and counseling

Collaborators, Affiliations

Evidence-based consensus guidelines for ALS genetic testing and counseling

Jennifer Roggenbuck et al. Ann Clin Transl Neurol. 2023 Nov.

Abstract

Objective: Advances in amyotrophic lateral sclerosis (ALS) gene discovery, ongoing gene therapy trials, and patient demand have driven increased use of ALS genetic testing. Despite this progress, the offer of genetic testing to persons with ALS is not yet "standard of care." Our primary goal is to develop clinical ALS genetic counseling and testing guidelines to improve and standardize genetic counseling and testing practice among neurologists, genetic counselors or any provider caring for persons with ALS.

Methods: Core clinical questions were identified and a rapid review performed according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA-P) 2015 method. Guideline recommendations were drafted and the strength of evidence for each recommendation was assessed by combining two systems: the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) System and the Evaluation of Genomic Applications in Practice and Prevention (EGAPP). A modified Delphi approach was used to reach consensus among a group of content experts for each guideline statement.

Results: A total of 35 guideline statements were developed. In summary, all persons with ALS should be offered single-step genetic testing, consisting of a C9orf72 assay, along with sequencing of SOD1, FUS, and TARDBP, at a minimum. The key education and genetic risk assessments that should be provided before and after testing are delineated. Specific guidance regarding testing methods and reporting for C9orf72 and other genes is provided for commercial laboratories.

Interpretation: These evidence-based, consensus guidelines will support all stakeholders in the ALS community in navigating benefits and challenges of genetic testing.

PubMed Disclaimer

Conflict of interest statement

JR has served as a consultant for Biogen, Ionis, and Uniqure. MH has served as a consultant for Biogen, Amylyx, Invitae, Guidepoint Global, and MDA. BE, JW, and SK have no conflicts to declare.

Figures

Figure 1
Figure 1
Summary of methods for guidelines development. GRADE; Grading of Recommendations, Assessment, Development and Evaluation; EGAPP, Evaluation of Genomic Applications in Practice and Prevention.
Figure 2
Figure 2
PRISMA‐P flow diagram of the identified studies (263 articles were included in the rapid review).
Figure 3
Figure 3
Modified Delphi methodology and results.
Figure 4
Figure 4
Summary of clinical testing guidelines. ClinGen, Clinical Genome Resource, https://clinicalgenome.org/affiliation/40096/.
Figure 5
Figure 5
Summary of genetic counseling recommendations.
Figure 6
Figure 6
Summary of laboratory recommendations. PCR, polymerase chain reaction; WGS, whole‐genome sequencing.

Similar articles

Cited by

References

    1. Arthur KC, Doyle C, Chiò A, Traynor BJ. Use of genetic testing in amyotrophic lateral sclerosis by neurologists. JAMA Neurol. 2017;74(1):125‐126. - PMC - PubMed
    1. Byrne S, Elamin M, Bede P, Hardiman O. Absence of consensus in diagnostic criteria for familial neurodegenerative diseases. J Neurol Neurosurg Psychiatry. 2012;83(4):365‐367. - PubMed
    1. Chia R, Chiò A, Traynor BJ. Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications. Lancet Neurol. 2018;17(1):94‐102. - PMC - PubMed
    1. Klepek H, Nagaraja H, Goutman SA, Quick A, Kolb SJ, Roggenbuck J. Lack of consensus in ALS genetic testing practices and divergent views between ALS clinicians and patients. Amyotroph Lateral Scler Front Degener. 2019;20(3–4):216‐221. - PMC - PubMed
    1. Vajda A, McLaughlin RL, Heverin M, et al. Genetic testing in ALS: a survey of current practices. Neurology. 2017;88(10):991‐999. - PMC - PubMed

MeSH terms

Substances