Back to Search Start Over

Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families.

Authors :
Janin N
Andrieu N
Ossian K
Laugé A
Croquette MF
Griscelli C
Debré M
Bressac-de-Paillerets B
Aurias A
Stoppa-Lyonnet D
Source :
British journal of cancer [Br J Cancer] 1999 Jun; Vol. 80 (7), pp. 1042-5.
Publication Year :
1999

Abstract

Epidemiological studies in ataxia telangiectasia (AT) families have suggested that AT heterozygotes could have an increased cancer risk, especially breast cancer (BC) in women. It has also been suggested that an increased sensibility of AT heterozygotes to the effect of ionizing radiation could be responsible for the increased BC risk. BC relative risk (RR) estimation in AT heterozygotes within families ascertained through AT children is presented here. Family data collected included demographic characteristics, occurrence of cancers, past radiation exposures and blood samples. DNA samples were studied using seven ATM linked microsatellites markers allowing AT haplotypes reconstitution. The relative risk of BC was assessed using French estimated incidence rates. A significant increase risk of BC is found among obligate ATM heterozygotes with a point estimate of 3.32 (P = 0.002). BC relative risk calculated according to age is significantly increased among the obligate ATM heterozygotes female relatives with an age < or = 44 years (RR = 4.55, P = 0.005). The BC relative risk is statistically borderline among the obligate ATM heterozygote female relatives with an age > or = 45 years (RR = 2.48, P = 0.08). The estimated BC relative risk among ATM heterozygotes is consistent with previously published data. However, the increased risk is only a little higher than classical reproductive risk factors and similar to the risk associated with a first-degree relative affected by BC.

Details

Language :
English
ISSN :
0007-0920
Volume :
80
Issue :
7
Database :
MEDLINE
Journal :
British journal of cancer
Publication Type :
Academic Journal
Accession number :
10362113
Full Text :
https://doi.org/10.1038/sj.bjc.6690460