Claus Jason, Schoof Lauritz, Mir Thomas S, Kammal Anna Lena, Schön Gerhard, Kutsche Kerstin, Behrendt Christian-Alexander, Kallenbach Klaus, Kölbel Tilo, Kubisch Christian, Demal Till Joscha, Petersen Johannes, Brickwedel Jens, Hübler Michael, Detter Christian, Kirchhof Paulus, Debus Eike Sebastian, Rybczynski Meike, von Kodolitsch Yskert
Division of Cardiology, Heart Surgery and Vascular Surgery, University Heart & Vascular Center Hamburg, All University Medical Center Eppendorf, Hamburg, Germany.
Division of Cardiology, Heart Surgery and Vascular Surgery, University Heart & Vascular Center Hamburg, All University Medical Center Eppendorf, Hamburg, Germany; Division of Cardiology, VASCERN-HTAD Affiliated Partner-Centre, Hamburg, Germany.
J Thorac Cardiovasc Surg. 2025 Apr;169(4):1201-1209.e33. doi: 10.1016/j.jtcvs.2024.09.016. Epub 2024 Sep 19.
Marfan syndrome (MFS) guidelines recommend optimal pharmacologic therapy (OPT) and replacement of the ascending aorta (RAA) at 5.0 cm in diameter to prevent acute type A aortic dissection (ATAAD) and death. The effect of early MFS diagnosis and initiation of therapy on outcomes is not known. Therefore, we sought to evaluate the effect of age at MFS diagnosis and therapy initiation on delayed RAA and death.
This retrospective observational cohort study with long-term follow-up included consecutive patients with MFS, pathogenic FBN1 variant, and regular visits to a European Reference Network Center. We considered MFS diagnosis at age ≥21 years late and OPT initiation at age <21 years early. Outcomes were delayed RAA with aneurysm diameter >5.0 cm or ATAAD and death from all causes. We used landmark design starting at age 21 years to determine associations with outcomes.
The study group consisted of 288 patients (45.1% male), including 169 patients with late diagnosis of MFS (58.7%) and 63 with early OPT (21.9%). During mean follow-up of 25 ± 14.7 years, 78 patients had delayed RAA, with 42 operations for ATAAD and 36 for aneurysms ≥5.0 cm. There were 33 deaths, including 11 deaths late after ATAAD. All deaths were cardiovascular. Late diagnosis, but not early OPT, showed univariate association with delayed RAA (P < .001) and death (P = .025). Multivariate Cox regression analysis confirmed late diagnosis as predictor of delayed RAA (hazard ratio, 8.01; 95% confidence interval, 2.52-25.45; P < .001) and death (hazard ratio, 4.68; 95% confidence interval, 1.17-18.80; P = .029).
Late diagnosis of MFS is associated with delayed surgery and death.
马凡综合征(MFS)指南推荐进行最佳药物治疗(OPT),并在升主动脉直径达到5.0厘米时进行升主动脉置换术(RAA),以预防A型主动脉夹层(ATAAD)急性发作和死亡。早期诊断MFS并开始治疗对预后的影响尚不清楚。因此,我们试图评估MFS诊断和开始治疗时的年龄对延迟性RAA和死亡的影响。
这项具有长期随访的回顾性观察队列研究纳入了连续的MFS患者、携带致病性FBN1变异且定期就诊于欧洲参考网络中心的患者。我们将≥21岁时诊断MFS视为诊断延迟,将<21岁时开始OPT视为早期开始治疗。结局指标为动脉瘤直径>5.0厘米的延迟性RAA或ATAAD以及全因死亡。我们采用从21岁开始的标志性设计来确定与结局的关联。
研究组包括288例患者(45.1%为男性),其中169例MFS诊断延迟(58.7%),63例早期开始OPT(21.9%)。在平均25±14.7年的随访期间,78例患者出现延迟性RAA,其中42例因ATAAD接受手术,36例因动脉瘤≥5.0厘米接受手术。有33例死亡,其中11例在ATAAD晚期死亡。所有死亡均为心血管原因导致。诊断延迟而非早期OPT显示与延迟性RAA(P<.001)和死亡(P=.025)存在单变量关联。多变量Cox回归分析证实诊断延迟是延迟性RAA(风险比,8.01;95%置信区间,2.52 - 25.45;P<.001)和死亡(风险比,4.68;95%置信区间,1.17 - 18.80;P=.029)的预测因素。
MFS诊断延迟与手术延迟和死亡相关。