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Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study

Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study
Objective: To obtain penetrance data for Huntington’s disease when DNA results are in the range of 36–39 CAG repeats and assess the consistency of reporting the upper allele from two reference centres.
Method: Data were collected anonymously on age of onset or age last known to be unaffected from a cohort of individuals with results in this range. DNA samples were re-analysed in two reference centres. Kaplan-Meier analysis was used to construct an age of onset curve and penetrance figures.
Results: Clinical data and concordant DNA results from both reference centres were available for 176 samples; penetrance figures (and 95% confidence intervals) for this cohort, at age 65 and 75 years, were 63.9% (55.5% to 73.2%) and 74.2% (64.2% to 84.2%), respectively. Inclusion of 28 additional subjects for whom repeat DNA results were unavailable, obtained from only one reference centre, or discrepant by one repeat within this range, gave penetrance data (including 95% confidence intervals) at ages 65 and 75 years of 62.4% (54.4% to 70.4%) and 72.7.% (63.3% to 82.1%), respectively. 238 duplicate results were available from the reference centres; 10 (4.2%) differed by one CAG repeat in the reporting of the upper allele and in two (0.84%) of these cases the discrepancy was between 39 and 40 repeats.
Conclusion: When DNA results are in this range, a conservative approach is to say that there is at least a 40% chance the person will be asymptomatic at age 65 years and at least a 30% chance the person will be asymptomatic at age 75 years.
london, trinucleotide repeat, confidence intervals, disease, chromosomes, alleles, age of onset, children, england, scotland, ireland, australia, netherlands, dna, prediction, time, onset
0022-2593
e68-[6pp]
Quarrell, Oliver W.J.
f28de12d-fa22-4eba-a8e6-c0dfeaa9bf16
Rigby, Alan S.
5e99bc17-6d8a-4ac6-9a3c-7266119c185f
Barron, L.
ee0cdb9d-7225-45bd-ba5f-aa7f564e492e
Crow, Y.
60599f78-39e1-4ce0-a5e4-fcdd225dacd4
Dalton, A.
9815a72b-7cd1-4a71-bb47-295028dab99b
Dennis, N.
154aa617-52e2-4711-98ef-89fef8610de7
Fryer, A.E.
c517fa13-acf2-491a-801d-1bf3e752451a
Heydon, F.
dd590531-3238-492a-81a3-e0622463b202
Kinning, E.
f44f67d2-8635-4a63-86a6-27009896ed54
Lashwood, A.
408c6104-1768-482c-b0ab-f8a06df817b6
Losekoot, M.
55aa6212-25b0-4ee4-905c-f9dd3e2201dd
Margerison, L.
df590bc5-f0e0-4477-9f0f-4e93883e565d
McDonnell, S.
2c0479ae-cc2f-4334-a0cc-919349982ac9
Morrison, P.J.
cdcdba90-397b-4345-b409-7e2d1e1282d4
Norman, A.
880800e2-eabd-4e44-847f-ca6f4321c5aa
Peterson, M.
692fc059-3987-4815-984e-d51eeff6a0c8
Raymond, F.L.
c6247c75-486e-4534-b202-7727933c96cd
Simpson, S.
a4621e58-7bbb-4cd3-bd0b-218886ab2b4e
Thompson, E.
fee77a63-09fc-4dca-b1d3-777f368ebe3e
Warner, J.
a7bcf9ec-794a-4cc5-8498-7d13d8b5927d
Quarrell, Oliver W.J.
f28de12d-fa22-4eba-a8e6-c0dfeaa9bf16
Rigby, Alan S.
5e99bc17-6d8a-4ac6-9a3c-7266119c185f
Barron, L.
ee0cdb9d-7225-45bd-ba5f-aa7f564e492e
Crow, Y.
60599f78-39e1-4ce0-a5e4-fcdd225dacd4
Dalton, A.
9815a72b-7cd1-4a71-bb47-295028dab99b
Dennis, N.
154aa617-52e2-4711-98ef-89fef8610de7
Fryer, A.E.
c517fa13-acf2-491a-801d-1bf3e752451a
Heydon, F.
dd590531-3238-492a-81a3-e0622463b202
Kinning, E.
f44f67d2-8635-4a63-86a6-27009896ed54
Lashwood, A.
408c6104-1768-482c-b0ab-f8a06df817b6
Losekoot, M.
55aa6212-25b0-4ee4-905c-f9dd3e2201dd
Margerison, L.
df590bc5-f0e0-4477-9f0f-4e93883e565d
McDonnell, S.
2c0479ae-cc2f-4334-a0cc-919349982ac9
Morrison, P.J.
cdcdba90-397b-4345-b409-7e2d1e1282d4
Norman, A.
880800e2-eabd-4e44-847f-ca6f4321c5aa
Peterson, M.
692fc059-3987-4815-984e-d51eeff6a0c8
Raymond, F.L.
c6247c75-486e-4534-b202-7727933c96cd
Simpson, S.
a4621e58-7bbb-4cd3-bd0b-218886ab2b4e
Thompson, E.
fee77a63-09fc-4dca-b1d3-777f368ebe3e
Warner, J.
a7bcf9ec-794a-4cc5-8498-7d13d8b5927d

Quarrell, Oliver W.J., Rigby, Alan S., Barron, L., Crow, Y., Dalton, A., Dennis, N., Fryer, A.E., Heydon, F., Kinning, E., Lashwood, A., Losekoot, M., Margerison, L., McDonnell, S., Morrison, P.J., Norman, A., Peterson, M., Raymond, F.L., Simpson, S., Thompson, E. and Warner, J. (2007) Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study. Journal of Medical Genetics, 44 (3), e68-[6pp]. (doi:10.1136/jmg.2006.045120).

Record type: Article

Abstract

Objective: To obtain penetrance data for Huntington’s disease when DNA results are in the range of 36–39 CAG repeats and assess the consistency of reporting the upper allele from two reference centres.
Method: Data were collected anonymously on age of onset or age last known to be unaffected from a cohort of individuals with results in this range. DNA samples were re-analysed in two reference centres. Kaplan-Meier analysis was used to construct an age of onset curve and penetrance figures.
Results: Clinical data and concordant DNA results from both reference centres were available for 176 samples; penetrance figures (and 95% confidence intervals) for this cohort, at age 65 and 75 years, were 63.9% (55.5% to 73.2%) and 74.2% (64.2% to 84.2%), respectively. Inclusion of 28 additional subjects for whom repeat DNA results were unavailable, obtained from only one reference centre, or discrepant by one repeat within this range, gave penetrance data (including 95% confidence intervals) at ages 65 and 75 years of 62.4% (54.4% to 70.4%) and 72.7.% (63.3% to 82.1%), respectively. 238 duplicate results were available from the reference centres; 10 (4.2%) differed by one CAG repeat in the reporting of the upper allele and in two (0.84%) of these cases the discrepancy was between 39 and 40 repeats.
Conclusion: When DNA results are in this range, a conservative approach is to say that there is at least a 40% chance the person will be asymptomatic at age 65 years and at least a 30% chance the person will be asymptomatic at age 75 years.

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Published date: 2007
Keywords: london, trinucleotide repeat, confidence intervals, disease, chromosomes, alleles, age of onset, children, england, scotland, ireland, australia, netherlands, dna, prediction, time, onset

Identifiers

Local EPrints ID: 60139
URI: http://eprints.soton.ac.uk/id/eprint/60139
ISSN: 0022-2593
PURE UUID: 1d750206-045f-4ba3-8267-8e1cfd3ce692

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Date deposited: 08 Sep 2008
Last modified: 15 Mar 2024 11:19

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Contributors

Author: Oliver W.J. Quarrell
Author: Alan S. Rigby
Author: L. Barron
Author: Y. Crow
Author: A. Dalton
Author: N. Dennis
Author: A.E. Fryer
Author: F. Heydon
Author: E. Kinning
Author: A. Lashwood
Author: M. Losekoot
Author: L. Margerison
Author: S. McDonnell
Author: P.J. Morrison
Author: A. Norman
Author: M. Peterson
Author: F.L. Raymond
Author: S. Simpson
Author: E. Thompson
Author: J. Warner

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