病例报告:重组生长激素治疗女童Loeys-Dietz综合征的疗效和安全性。

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Frontiers in Cardiovascular Medicine Pub Date : 2025-01-03 eCollection Date: 2024-01-01 DOI:10.3389/fcvm.2024.1377510
Kamil Dyrka, Aleksander Jamsheer, Michal Bartecki, Waldemar Bobkowski, Malgorzata Pawelec-Wojtalik, Justyna Rajewska-Tabor, Andzelika Tomaszewska, Justyna Balcerzak, Zuzanna Aniol, Marek Niedziela, Monika Obara-Moszynska
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引用次数: 0

摘要

背景:Loeys-Dietz综合征(LDS)是一种临床和遗传异质性的常染色体显性主动脉瘤综合征,具有广泛的全身累及。我们报告了一例16.5岁女孩的LDS2型(LDS2),由转化生长因子- β受体2型(TGFBR2)基因的杂合致病变异c.1582C>T (p.Arg528Cys)引起,由于共存的生长激素缺乏症(GHD),她接受了重组生长激素(rGH)治疗。本病例报告(观察性研究)介绍了rGH治疗的疗效和这种治疗的安全性,包括主动脉成像随访(超声心动图,ECHO)。据我们所知,这是第一次研究长期rGH治疗对LDS患者主动脉尺寸的影响。病例总结:患者在出生后2年被确认为LDS。3岁后,观察到生长减速。6岁时发现GHD[刺激后最大GH 7.2 ng/ml;胰岛素样生长因子-1 (IGF-1), 35 ng/ml;N: 84 - 447)。在6.5岁时,rGH开始(身高标准差评分,htSDS -2.4),持续到14.25年(htSDS-1.4)。她16.5岁时的身高是155厘米。rGH剂量为0.025 ~ 0.028 mg/kg/d。16个月后,通过超声心动图观察主动脉根部增宽。在近16岁时,由于主动脉根部扩张(Z评分+5.95),女孩接受了主动脉整形手术,获得了满意的结果。患者目前病情稳定,但由于LDS患者存在许多合并症,需要多学科合作进行管理。结论:虽然大多数LDS患者发生主动脉扩张,但生长激素治疗对主动脉大小的可能影响必须考虑。然而,生长激素活性的主要生化标志物IGF-1是否与主动脉直径增加独立相关尚未确定。除了促进生长的作用,生长激素对人体、代谢状态和肌肉力量的广泛影响也是显著的。本例患者在rGH治疗前极低的IGF-1水平以及在rGH给药期间严格监测IGF1/IGFBP3比值似乎是安全且有利于治疗的。
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Case Report: Efficacy and safety of recombinant growth hormone therapy in a girl with Loeys-Dietz syndrome.

Background: Loeys-Dietz syndrome (LDS) is a clinically and genetically heterogeneous, autosomal dominant aortic aneurysm syndrome with widespread systemic involvement. We present the case of a 16.5-year-old girl with LDS type 2 (LDS2) caused by a heterozygous pathogenic variant, c.1582C>T (p.Arg528Cys), in the transforming growth factor-beta receptor type 2 (TGFBR2) gene who was treated with recombinant growth hormone (rGH) due to coexisting GH deficiency (GHD). This case report (observational study) presents the efficacy of rGH therapy and the safety aspects of this treatment, including aortal imaging follow-up (echocardiography, ECHO). To our knowledge, this is the first investigation of the effects of long-term rGH treatment on aortic dimensions in an LDS patient.

Case summary: LDS was recognized in the patient in the 2nd year of life. After the 3rd year of life, growth deceleration was observed. At age 6, GHD was recognized [the maximum GH after stimulation 7.2 ng/ml; insulin-like growth factor-1 (IGF-1), 35 ng/ml; N: 84-447]. At age 6.5 years, rGH was initiated (height standard deviation score, htSDS -2.4), which continued for up to 14.25 years (htSDS-1.4). Her height at 16.5 years was 155 cm. The dose of rGH was 0.025-0.028 mg/kg/day. After the age of 16 months, widening of the aortic root was observed via echocardiography. At nearly 16 years, due to dilated aortic root (Z score +5.95), the girl underwent a plastic operation on the aorta, which had a satisfactory outcome. The patient's current status is stable, but the management of patients with LDS requires multidisciplinary cooperation due to the many coexisting comorbidities.

Conclusions: Although aortic dilatation occurs in most LDS patients, the possible influence of GH therapy on aortic size must be considered. However, whether IGF-1, the main biochemical marker of GH activity, can be independently associated with increased aortic diameter has not been determined. In addition to its growth-promoting effect, the wide influence of GH on the human body, metabolic status, and muscle strength is also significant. The extremely low IGF-1 level before rGH therapy in the present patient and the strict monitoring of the IGF1/IGFBP3 ratio during rGH administration seem to be safe and beneficial for therapy.

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来源期刊
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.80
自引率
11.10%
发文量
3529
审稿时长
14 weeks
期刊介绍: Frontiers? Which frontiers? Where exactly are the frontiers of cardiovascular medicine? And who should be defining these frontiers? At Frontiers in Cardiovascular Medicine we believe it is worth being curious to foresee and explore beyond the current frontiers. In other words, we would like, through the articles published by our community journal Frontiers in Cardiovascular Medicine, to anticipate the future of cardiovascular medicine, and thus better prevent cardiovascular disorders and improve therapeutic options and outcomes of our patients.
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