Absence of linkage of familial intracranial aneurysms to 7q11 in highly aggregated Japanese families

被引:31
作者
Yamada, S
Utsunomiya, M
Inoue, K
Nozaki, K
Miyamoto, S
Hashimoto, N
Takenaka, K
Yoshinaga, T
Koizumi, A [1 ]
机构
[1] Kyoto Univ, Dept Hlth & Environm Sci, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Dept Neurosurg, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
[3] Takayama Red Cross Hosp, Dept Neurosurg, Gifu, Japan
关键词
aneurysm; intracranial; elastin; genetics;
D O I
10.1161/01.STR.0000062887.71400.B4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-We sought to test the linkage of familial intracranial aneurysms (FIAs) to the ELN (elastin) locus in chromosome 7q11 reported previously. Methods-Intracranial aneurysm (IA) probands were searched from patient records or neurosurgeons' recalls in collaborating hospitals. Members of the participating probands' families who had unknown affection status were screened by MR angiography and diagnosed by digital subtraction angiography. Inclusion criteria of families for genetic analyses were as follows: at least 3 alive affected members or 2 alive affected members with at least 1 unaffected member (greater than or equal to60 years). Linkage to the ELN locus was tested with the use of GENEHUNTER by parametric and nonparametric methods. To exclude false-negatives in the linkage analysis, the lowest 5% limits of logarithms of the odds (LOD) and nonparametric LOD (NPL) scores for individual families and for the total set of families were simulated on assumption that the ELN locus is linked to FIAs. Results-Questionnaires were sent to 885 patients, and 563 responded. Seventy-nine probands were positive for family history. One hundred thirty-four family members of unknown affection status were screened. A total of 14 families with 64 members met the criteria. Linkage to the ELN locus was discarded in 11 families and was inconclusive for 3 families. The total LOD and total NPL scores for 14 families were -8.04 and -0.643, respectively. Our conclusion did not change even when the values of penetrance were changed or only affected members were analyzed. Conclusions-The majority of aggregated IA Japanese families may not have a genetic linkage to chromosome 7q11.
引用
收藏
页码:892 / 900
页数:9
相关论文
共 35 条
[1]   ARE CEREBRAL ANEURYSMS ATHEROSCLEROTIC [J].
ADAMSON, J ;
HUMPHRIES, SE ;
OSTERGAARD, JR ;
VOLDBY, B ;
RICHARDS, P ;
POWELL, JT .
STROKE, 1994, 25 (05) :963-966
[2]   Heterogeneity for multiple disease loci in linkage analysis [J].
Bhat, A ;
Heath, SC ;
Ott, J .
HUMAN HEREDITY, 1999, 49 (04) :229-231
[3]   Genotypic variations of type III collagen in patients with cerebral aneurysms [J].
Brega, KE ;
Seltzer, WK ;
Munro, LG ;
Breeze, RE .
SURGICAL NEUROLOGY, 1996, 46 (03) :253-256
[4]   OUTCOME IN FAMILIAL SUBARACHNOID HEMORRHAGE [J].
BROMBERG, JEC ;
RINKEL, GJE ;
ALGRA, A ;
LIMBURG, M ;
VANGIJN, J .
STROKE, 1995, 26 (06) :961-963
[5]   Influence of smoking, hypertension, and sex on the phenotypic expression of familial intracranial aneurysms in siblings [J].
Connolly, ES ;
Choudhri, TF ;
Mack, WJ ;
Mocco, J ;
Spinks, TJ ;
Slosberg, J ;
Lin, T ;
Huang, J ;
Solomon, RA .
NEUROSURGERY, 2001, 48 (01) :64-68
[6]   Trends in incidence and case fatality rates of aneurysmal subarachnoid hemorrhage in Izumo City, Japan, between 1980-1989 and 1990-1998 [J].
Inagawa, T .
STROKE, 2001, 32 (07) :1499-1507
[7]   Prevalence of intracranial saccular aneurysms in a Japanese community based on a consecutive autopsy series during a 30-year observation period - The Hisayama study [J].
Iwamoto, H ;
Kiyohara, Y ;
Fujishima, M ;
Kato, I ;
Nakayama, K ;
Sueishi, K ;
Tsuneyoshi, M .
STROKE, 1999, 30 (07) :1390-1395
[8]   Factors affecting formation and growth of intracranial aneurysms - A long-term follow-up study [J].
Juvela, S ;
Poussa, K ;
Porras, M .
STROKE, 2001, 32 (02) :485-491
[9]   Clinical features of intracranial aneurysms in siblings [J].
Kasuya, H ;
Onda, H ;
Takeshita, M ;
Hori, T ;
Takakura, K .
NEUROSURGERY, 2000, 46 (06) :1301-1305
[10]   The ACE I allele is associated with increased risk for ruptured intracranial aneurysms [J].
Keramatipour, M ;
McConnell, RS ;
Kirkpatrick, P ;
Tebbs, S ;
Furlong, RA ;
Rubinsztein, DC .
JOURNAL OF MEDICAL GENETICS, 2000, 37 (07) :498-500