Aneurysm syndromes caused by mutations in the TGF-β receptor

被引:1165
作者
Loeys, Bart L.
Schwarze, Ulrike
Holm, Tammy
Callewaert, Bert L.
Thomas, George H.
Pannu, Hariyadarshi
De Backer, Julie F.
Oswald, Gretchen L.
Symoens, Sofie
Manouvrier, Sylvie
Roberts, Amy E.
Faravelli, Francesca
Greco, M. Alba
Pyeritz, Reed E.
Milewicz, Dianna M.
Coucke, Paul J.
Cameron, Duke E.
Braverman, Alan C.
Byers, Peter H.
De Paepe, Anne M.
Dietz, Harry C.
机构
[1] State Univ Ghent Hosp, Ctr Genet Med, B-9000 Ghent, Belgium
[2] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Surg, Baltimore, MD 21205 USA
[4] Kennedy Krieger Inst, Baltimore, MD USA
[5] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[6] Univ Washington, Dept Med, Seattle, WA USA
[7] Univ Texas, Dept Med, Houston, TX USA
[8] Univ Hosp, Dept Clin Genet, Lille, France
[9] Harvard Univ, Sch Med, Dept Clin Genet, Boston, MA USA
[10] Osped Galliera, Dept Human Genet, Genoa, Italy
[11] NYU, Sch Med, Dept Pathol, New York, NY USA
[12] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[13] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[14] Howard Hughes Med Inst, Chevy Chase, MD USA
关键词
D O I
10.1056/NEJMoa055695
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The Loeys-Dietz syndrome is a recently described autosomal dominant aortic-aneurysm syndrome with widespread systemic involvement. The disease is characterized by the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate and is caused by heterozygous mutations in the genes encoding transforming growth factor (beta) receptors 1 and 2 (TGFBR1 and TGFBR2, respectively). Methods: We undertook the clinical and molecular characterization of 52 affected families. Forty probands presented with typical manifestations of the Loeys-Dietz syndrome. In view of the phenotypic overlap between this syndrome and vascular Ehlers-Danlos syndrome, we screened an additional cohort of 40 patients who had vascular Ehlers-Danlos syndrome without the characteristic type III collagen abnormalities or the craniofacial features of the Loeys-Dietz syndrome. Results: We found a mutation in TGFBR1 or TGFBR2 in all probands with typical Loeys-Dietz syndrome (type I) and in 12 probands presenting with vascular Ehlers-Danlos syndrome (Loeys-Dietz syndrome type II). The natural history of both types was characterized by aggressive arterial aneurysms (mean age at death, 26.0 years) and a high incidence of pregnancy-related complications (in 6 of 12 women). Patients with Loeys-Dietz syndrome type I, as compared with those with type II, underwent cardiovascular surgery earlier (mean age, 16.9 years vs. 26.9 years) and died earlier (22.6 years vs. 31.8 years). There were 59 vascular surgeries in the cohort, with one death during the procedure. This low rate of intraoperative mortality distinguishes the Loeys-Dietz syndrome from vascular Ehlers-Danlos syndrome. Conclusions: Mutations in either TGFBR1 or TGFBR2 predispose patients to aggressive and widespread vascular disease. The severity of the clinical presentation is predictive of the outcome. Genotyping of patients presenting with symptoms like those of vascular Ehlers-Danlos syndrome may be used to guide therapy, including the use and timing of prophylactic vascular surgery.
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收藏
页码:788 / 798
页数:11
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