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
. 2002 Apr;70(4):985-93.
doi: 10.1086/339815. Epub 2002 Mar 1.

Age at onset in two common neurodegenerative diseases is genetically controlled

Affiliations

Age at onset in two common neurodegenerative diseases is genetically controlled

Yi-Ju Li et al. Am J Hum Genet. 2002 Apr.

Abstract

To identify genes influencing age at onset (AAO) in two common neurodegenerative diseases, a genomic screen was performed for AAO in families with Alzheimer disease (AD; n=449) and Parkinson disease (PD; n=174). Heritabilities between 40%--60% were found in both the AD and PD data sets. For PD, significant evidence for linkage to AAO was found on chromosome 1p (LOD = 3.41). For AD, the AAO effect of APOE (LOD = 3.28) was confirmed. In addition, evidence for AAO linkage on chromosomes 6 and 10 was identified independently in both the AD and PD data sets. Subsequent unified analyses of these regions identified a single peak on chromosome 10q between D10S1239 and D10S1237, with a maximum LOD score of 2.62. These data suggest that a common gene affects AAO in these two common complex neurodegenerative diseases.

PubMed Disclaimer

Figures

Figure  1
Figure 1
Results of chromosome 10 multipoint linkage analyses. Marker distances were based on sex-averaged Kosambi centimorgans according to Map-O-Mat.
Figure  2
Figure 2
Map positions of reported linkage results for the risk and AAO genes on chromosome 10q.

References

Electronic-Database Information

    1. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/ (for AD [MIM 104300] and PD [MIM 168600])
    1. Map-O-Mat, http://compgen.rutgers.edu/mapomat/

References

    1. Abbas N, Lucking CB, Ricard S, Durr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Brousolle E, Brefel-Courbon C, Harhangi S, Oostra B, Fabrizio E, Bohme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A, The French Parkinson's Disease Study Group, The European Consortium on Genetic Susceptibility in Parknson's Disease (1999) A wide variety of mutations in the Parkin gene are responsible for autosomal recessive parkinsonism in Europe. Hum Mol Genet 8:567–574 - PubMed
    1. Almasy L, Blangero J (1998) Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 62:1198–1211 - PMC - PubMed
    1. Amos CI (1994) Robust variance-components approach for assessing genetic linkage in pedigrees. Am J Hum Genet 54:535–543 - PMC - PubMed
    1. Bertram L, Blacker D, Mullin K, Keeney D, Jones J, Basu S, Yhu S, McInnis M, Go RCP, Vekrellis K, Selkoe DJ, Saunders A, Tanzi R (2000) Evidence for genetic linkage of Alzheimer's disease to chromosome 10q. Science 290:2302–2305 - PubMed
    1. Blangero J, Almasy L (1997) Multipoint oligogenic linkage analysis of quantitative traits. Genet Epidemiol 14:959–964 - PubMed

Publication types

Substances

Associated data