Suppr超能文献

用于鉴别遗传性转甲状腺素蛋白淀粉样多神经病与特发性轴索性多神经病的危险信号和调整后的可疑指数。

Red flags and adjusted suspicion index for distinguishing hereditary transthyretin amyloid polyneuropathy from idiopathic axonal polyneuropathy.

机构信息

Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, 3584 CX, Utrecht, The Netherlands.

Department of Genetics, University Medical Center Utrecht, 3584 CX, Utrecht, The Netherlands.

出版信息

Neurol Sci. 2023 Oct;44(10):3679-3685. doi: 10.1007/s10072-023-06859-w. Epub 2023 Jun 2.

Abstract

BACKGROUND

Early diagnosis of hereditary ATTR polyneuropathy (ATTRv-PN) is important since treatment options have become available, which are most effective early in the disease course. ATTRv-PN is likely underdiagnosed as patients might be misdiagnosed with idiopathic polyneuropathy. It is uncertain if it is useful to test for TTR gene mutations in patients with a typical presentation for chronic idiopathic axonal polyneuropathy (CIAP) and which are the distinguishing clinical features.

METHODS

We carried out a retrospective cohort study to assess the yield of TTR gene sequencing in patients with polyneuropathy and assessed if the identified patients with ATTRv-PN had a clinical presentation typical of CIAP. Additionally, we assessed which clinical features, including previously defined red flag symptoms, can differentiate between patients with CIAP and ATTRv-PN and assessed the performance of the TTR suspicion index.

RESULTS

Out of 338 patients with polyneuropathy, 10 patients had a pathogenic TTR gene mutation (all p.Val50Met) and none had a clinical presentation typical of CIAP. Patients with ATTRv-PN more often had bilateral CTS, motor involvement of arms, cardiac involvement, family history suggestive of hATTRv, and autonomic symptoms than patients with CIAP. All patients with ATTRv-PN as well as 70% of patients with CIAP fulfilled the suspicion index.

CONCLUSION

Routine TTR gene sequencing in patients with a typical presentation for CIAP is not useful. However, red flag symptoms can differentiate patients with ATTRv-PN from patients with CIAP. We propose an adjusted version of the TTR suspicion index to increase diagnostic yield.

摘要

背景

由于治疗方法已经出现,遗传性转甲状腺素蛋白淀粉样变性多发性神经病(ATTRv-PN)的早期诊断非常重要,因为这些治疗方法在疾病早期最有效。由于患者可能被误诊为特发性多发性神经病,因此ATTRv-PN 可能被漏诊。对于表现为慢性特发性轴索性多发性神经病(CIAP)且具有独特临床特征的患者,检测 TTR 基因突变是否有用尚不确定。

方法

我们进行了一项回顾性队列研究,以评估在多发性神经病患者中进行 TTR 基因测序的效果,并评估确定的 ATTRv-PN 患者是否具有 CIAP 的典型表现。此外,我们评估了哪些临床特征(包括先前定义的红色预警症状)可以区分 CIAP 和 ATTRv-PN 患者,并评估了 TTR 可疑指数的性能。

结果

在 338 名患有多发性神经病的患者中,有 10 名患者存在致病性 TTR 基因突变(均为 p.Val50Met),且没有一名患者具有 CIAP 的典型表现。与 CIAP 患者相比,ATTRv-PN 患者更常出现双侧 CTS、手臂运动受累、心脏受累、提示 hATTRv 的家族史和自主神经症状。所有 ATTRv-PN 患者以及 70%的 CIAP 患者均符合可疑指数。

结论

对于表现为 CIAP 典型表现的患者,常规进行 TTR 基因测序没有用。但是,红色预警症状可以区分 ATTRv-PN 患者和 CIAP 患者。我们提出了 TTR 可疑指数的调整版本,以提高诊断效果。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验