Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1998 Apr;35(4):305–308. doi: 10.1136/jmg.35.4.305

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

M C Speer 1, J M Gilchrist 1, J M Stajich 1, P C Gaskell 1, C A Westbrook 1, S K Horrigan 1, L Bartoloni 1, L H Yamaoka 1, W K Scott 1, M A Pericak-Vance 1
PMCID: PMC1051279  PMID: 9598725

Abstract

Anticipation, an increase in severity or decrease in age of onset (AO) inherent in the transmission of the disease gene from affected parent to affected child, has been increasingly described in human disease. To assess anticipation in a large kindred in which autosomal dominant limb-girdle muscular dystrophy (LGMD1A) is segregating, age of disease onset was collected from patient interviews of affected family members. A total of 25 parent-offspring pairs, in which the parents are three (3R), four (4R), or five (5R) generations removed from a common founding ancestor, were available for analysis. Life table analyses showed significant decreases in age at first reported symptoms in the offspring of the 3R (chi2=5.55, p=0.02) and 4R (chi2=7.81, p=0.005) parents. Pairwise analyses confirmed this decrease with a median decrease of 13 years in transmission to offspring from 3R parents and 18 years in transmission to offspring from 4R parents. The finding of anticipation in this pedigree suggests that the mutation in LGMD1A may be the result of the expansion of an unstable trinucleotide repeat.

Full text

PDF
308

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chutkow J. G., Heffner R. R., Jr, Kramer A. A., Edwards J. A. Adult-onset autosomal dominant limb-girdle muscular dystrophy. Ann Neurol. 1986 Aug;20(2):240–248. doi: 10.1002/ana.410200210. [DOI] [PubMed] [Google Scholar]
  2. Gilchrist J. M., Pericak-Vance M., Silverman L., Roses A. D. Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy. Neurology. 1988 Jan;38(1):5–9. doi: 10.1212/wnl.38.1.5. [DOI] [PubMed] [Google Scholar]
  3. Harper P. S., Harley H. G., Reardon W., Shaw D. J. Anticipation in myotonic dystrophy: new light on an old problem. Am J Hum Genet. 1992 Jul;51(1):10–16. [PMC free article] [PubMed] [Google Scholar]
  4. Kawaguchi Y., Okamoto T., Taniwaki M., Aizawa M., Inoue M., Katayama S., Kawakami H., Nakamura S., Nishimura M., Akiguchi I. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet. 1994 Nov;8(3):221–228. doi: 10.1038/ng1194-221. [DOI] [PubMed] [Google Scholar]
  5. Lathrop G. M., Lalouel J. M., Julier C., Ott J. Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3443–3446. doi: 10.1073/pnas.81.11.3443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Mahadevan M., Tsilfidis C., Sabourin L., Shutler G., Amemiya C., Jansen G., Neville C., Narang M., Barceló J., O'Hoy K. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. Science. 1992 Mar 6;255(5049):1253–1255. doi: 10.1126/science.1546325. [DOI] [PubMed] [Google Scholar]
  7. McInnis M. G., McMahon F. J., Chase G. A., Simpson S. G., Ross C. A., DePaulo J. R., Jr Anticipation in bipolar affective disorder. Am J Hum Genet. 1993 Aug;53(2):385–390. [PMC free article] [PubMed] [Google Scholar]
  8. Speer M. C., Yamaoka L. H., Gilchrist J. H., Gaskell C. P., Stajich J. M., Vance J. M., Kazantsev A., Lastra A. A., Haynes C. S., Beckmann J. S. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q. Am J Hum Genet. 1992 Jun;50(6):1211–1217. [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES