The Role of the GH Receptor Polymorphisms as a Prognostic Factor of Vertebral Fractures in Acromegalic Patients Resistant to First-generation SSAs and Treated with Pegvisomant or Pasireotide LAR.

Flavia Costanza, Sabrina Chiloiro, Antonella Giampietro, Flavia Angelini, Amato Infante, Alfredo Pontecorvi, Laura De Marinis, Antonio Bianchi
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Abstract

Background: Acromegaly is associated with skeletal fragility and increased prevalence of vertebral fractures (VF). Two isoforms of GH receptor (GHR) have been described, which differ in the presence or absence of a transcript of exon 3 of the GHR gene. Both isoforms produce a functional receptor, but the exon 3-deleted isoforms (d3-GHR) have greater sensitivity to endogenous and recombinant GH than the full-length isoform (fl-GHR).

Objective: We conducted a longitudinal, retrospective, observational, single-center study to investigate the role of GHR polymorphism as a prognostic factor of incidental VF (I-VF) in firstgeneration somatostatin analogs (fg-SSAs)-resistant acromegalic patients and treated with Pegvisomant or Pasireotide LAR.

Methods: Seventy-two patients with active acromegaly were included: 28 patients carried the d3-GHR isoform, and 44 patients carried the fl-GHR isoform. Forty-six patients were treated with Pegvisomant in combination with fg-SSAs, and 26 were treated with Pasireotide LAR. At the last follow-up, 58 patients achieved biochemical control of acromegaly. Eighteen patients carried prevalent VF (P-VFs), while 14 patients experienced the occurrence of I-VFs.

Results: From the group treated with Pegvisomant in combination with fg-SSAs, 32 patients carried the fl-GHR isoform, and 14 carried the d3-GHR isoform. From the group treated with Pasireotide LAR, 12 patients had the fl-GHR isoform, and 14 patients carried the d3-GHR isoform. I-VF occurred more frequently in patients with the fl-GHR isoform compared to d3-GHR (p =0.04); otherwise, I-VF occurred more frequently in patients with the d3-GHR isoform than fl-GHR (p =0.01).

Conclusion: The GHR polymorphisms could improve the therapeutic approach in acromegaly, tailored to the individual patient, in the context of personalized medicine.

GH受体多态性作为对第一代SSAs耐药并接受Pegvisomant或Pasireotide LAR治疗的肢端肥大症患者椎体骨折预后因素的作用。
背景:肢端肥大症与骨骼脆弱和脊椎骨折(VF)发病率增加有关。GH 受体(GHR)有两种异构体,它们因 GHR 基因第 3 号外显子转录本的存在与否而不同。这两种异构体都能产生功能性受体,但外显子 3 缺失的异构体(d3-GHR)比全长异构体(fl-GHR)对内源性和重组 GH 更敏感:我们进行了一项纵向、回顾性、观察性、单中心研究,以调查 GHR 多态性作为第一代体生长抑素类似物(fg-SSAs)耐受性肢端肥大症患者偶发性 VF(I-VF)预后因素的作用,该患者接受了 Pegvisomant 或 Pasireotide LAR 治疗:纳入72例活动性肢端肥大症患者:28名患者携带d3-GHR同工酶,44名患者携带fl-GHR同工酶。46名患者接受了佩吉维松与fg-SSAs联合治疗,26名患者接受了帕西洛肽LAR治疗。在最后一次随访中,58 名患者的肢端肥大症得到了生化控制。18名患者出现了流行性肢端肥大症(P-VFs),14名患者出现了I-VFs:结果:在接受培维索孟联合 fg-SSAs 治疗的一组患者中,有 32 名患者携带 fl-GHR 同工酶,14 名患者携带 d3-GHR 同工酶。在帕西洛肽 LAR 治疗组中,12 名患者携带 fl-GHR 同工酶,14 名患者携带 d3-GHR 同工酶。与d3-GHR相比,fl-GHR异构体患者的I-VF发生率更高(P =0.04);此外,d3-GHR异构体患者的I-VF发生率也高于fl-GHR(P =0.01):结论:GHR多态性可在个性化医疗的背景下,改善针对个体患者的肢端肥大症治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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