共 26 条
Celiprolol Treatment in Patients with Vascular Ehlers-Danlos Synurome
被引:40
作者:

Baderkhan, Hassan
论文数: 0 引用数: 0
h-index: 0
机构:
Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden

Wanhainen, Anders
论文数: 0 引用数: 0
h-index: 0
机构:
Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden

Stenborg, Anna
论文数: 0 引用数: 0
h-index: 0
机构:
Uppsala Univ, Dept Med Sci, Uppsala, Sweden Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden

Stattin, Eva-Lena
论文数: 0 引用数: 0
h-index: 0
机构:
Uppsala Univ, Dept Clin Genet, Uppsala, Sweden Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden

Bjorck, Martin
论文数: 0 引用数: 0
h-index: 0
机构:
Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden
机构:
[1] Uppsala Univ, Vasc Surg, Dept Surg Sci, Uppsala, Sweden
[2] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[3] Uppsala Univ, Dept Clin Genet, Uppsala, Sweden
关键词:
Celiprolol;
COL3A1;
Drug therapy;
Ehlers-Danlos syndrome;
Pathogenic sequence variants;
Vascular type;
SYNDROME TYPE-IV;
PULSE PRESSURE;
MANAGEMENT;
COMPLICATIONS;
HYPERTROPHY;
PROGRESSION;
DISEASE;
D O I:
10.1016/j.ejvs.2020.10.020
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Objecti_ Vascular Ehlers-Danlos syndrome (vEDS) is a rare monogenetic disease caused by pathogenic variants in procollagen 3A1. Arterial rupture is the most serious clinical manifestation. A randomised controlled trial, the Beta-Blockers in Ehlers-Danlos Syndrome Treatment (BBEST) trial, reported a significant protective effect of the beta blocker celiprolol. The aim was to study the outcome of celiprolol treatment in a cohort of Swedish patients with vEDS. Methods: Uppsala is a national referral centre for patients with vEDS. They are assessed by vascular surgeons, angiologists, and clinical geneticists. Family history, previous and future clinical events, medication, and side effects are registered. Celiprolol was administered twice daily and titrated up to a maximum dose of 400 mg daily. Logistic regression was used to analyse predictors of vascular events. Results: Forty patients with pathogenic sequence variants in COL3A1 were offered treatment with celiprolol in the period 2011-2019. The median follow up was 22 months (range 1-98 months); total follow up was 106 patient years. In two patients, uptitration of the dose is ongoing. Of the remaining 38, 26 (65%) patients reached the target dose of 400 mg daily. Dose uptitration was unsuccessful in six patients because of side effects; one died before reaching the maximum dose, and five terminated the treatment. Five major vascular events occurred; four were fatal (ruptured ascending aorta; aortic rupture after type B dissection; ruptured cerebral aneurysm; and ruptured pulmonary artery). One bled from a branch of the internal iliac artery, which was successfully coiled endovascularly. The annual risk of a major vascular event was 4.7% (n = 5/106), similar to the treatment arm of the BBEST trial (5%) and lower than in the control arm of the same trial (12%). No significant predictor of vascular events was identified. Conclusion: Treatment with celiprolol is tolerated in most patients with vEDS. Despite fatal vascular events, these observations suggest that celiprolol may have a protective effect in vEDS.
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页码:326 / 331
页数:6
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