Servicio de Medicina Interna, Hospital Universitario Son Llàtzer, Crta Manacor Km 4, 07198, Palma, Balearic Islands, Spain.
Balearic Research Group in Genetic Cardiopathies, Sudden Death and TTR Amyloidosis, Instituto de Investigación Sanitaria de las Islas Baleares (IdISBa), Palma, Balearic Islands, Spain.
Orphanet J Rare Dis. 2021 Jun 10;16(1):266. doi: 10.1186/s13023-021-01910-5.
Hereditary transthyretin (TTR) amyloidosis (ATTRv) is a heterogeneous disease with a clinical presentation that varies according to geographical area and TTR mutation. The symptoms of Val50Met-ATTRv are mainly neuropathic and progress to complete disability and death in most untreated patients within 10 to 15 years of diagnosis. The neurological effects may also be accompanied by gastrointestinal impairment, cardiomyopathy, nephropathy and/or ocular deposition. The disease is thus associated with a high degree of patient disability. Accordingly, we aimed to describe the psychosocial burden associated with ATTRv in a group of patients, asymptomatic Val50Met carriers, relatives and caregivers in the endemic focus of the disease in Majorca via a survey addressing various aspects related to psychosocial burden. We performed a an observational, descriptive, cross-sectional and multicentre study in order to analyze the prevalence of self-reported impact of ATTRv disease upon their daily life. In addition to the self-knowledge, fear and burden related to the disease. The survey was disseminated during the regular follow up at the outpatient clinic of the Hospital Universitario Son Llàtzer and during the meetings organized by the Andrade's Disease patients' advocacy group from the Balearic Islands. These meetings were attended also by subjects followed up by the Hospital Universitario Son Espases and their caregivers and relatives. Survey was self-administrated. No intervention was done by the investigators. 85 subjects completed the survey: 61 carrying the TTR-V50M variant and 24 caregivers or relatives.
Our study revealed that, although most of the population studied had had prior contact with ATTRv through affected relatives, there was still a lack of information regarding disease diagnosis. Fear of the genetic test result and psychological issues were common in our population. Moreover, the disease had a stronger impact on the daily life of our patients than that of our asymptomatic carriers. Autonomic symptoms were the main source of burden for relatives and caregivers.
Our survey results show high psychosocial burden associated with Val50Met-ATTRv in our area.
遗传性转甲状腺素蛋白(TTR)淀粉样变(ATTRv)是一种异质性疾病,其临床表现因地理位置和 TTR 突变而异。Val50Met-ATTRv 的症状主要为神经病变,并在未经治疗的患者中,大多数在诊断后 10 到 15 年内进展为完全残疾和死亡。神经影响还可能伴有胃肠道损伤、心肌病、肾病和/或眼部沉积。因此,该疾病与患者高度残疾有关。因此,我们旨在通过一项涉及与心理社会负担相关的各个方面的调查,描述在马略卡岛疾病流行地区的一组患者、无症状 Val50Met 携带者、亲属和照顾者中与 ATTRv 相关的心理社会负担。我们进行了一项观察性、描述性、横断面和多中心研究,以分析自我报告的 ATTRv 疾病对日常生活的影响的患病率。除了与疾病相关的自我认识、恐惧和负担。该调查是在 Son Llàtzer 大学医院的门诊随访期间以及在巴利阿里群岛的 Andrade 疾病患者倡导团体组织的会议期间分发的。Son Espases 大学医院及其照顾者和亲属也参加了这些会议。调查是自我管理的。研究人员没有进行任何干预。共有 85 名受试者完成了调查:61 名携带 TTR-V50M 变体,24 名照顾者或亲属。
我们的研究表明,尽管大多数研究人群通过受影响的亲属已经接触过 ATTRv,但他们仍然缺乏关于疾病诊断的信息。对基因检测结果的恐惧和心理问题在我们的人群中很常见。此外,该疾病对我们患者的日常生活的影响比我们的无症状携带者更为严重。自主症状是亲属和照顾者负担的主要来源。
我们的调查结果表明,我们地区与 Val50Met-ATTRv 相关的心理社会负担很高。