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在混合性结缔组织病患者中,甲襞微血管异常与肺动脉高压的较高患病率相关。

Nailfold microvascular abnormalities are associated with a higher prevalence of pulmonary arterial hypertension in patients with MCTD.

作者信息

Todoroki Yasuyuki, Kubo Satoshi, Nakano Kazuhisa, Miyazaki Yusuke, Ueno Masanobu, Satoh-Kanda Yurie, Kanda Ryuichiro, Miyagawa Ippei, Hanami Kentaro, Nakatsuka Keisuke, Saito Kazuyoshi, Nakayamada Shingo, Tanaka Yoshiya

机构信息

First Department of Internal Medicine, University of Occupational and Environmental Health, Japan.

Department of Internal Medicine, Kitakyushu General Hospital, Kitakyushu, Japan.

出版信息

Rheumatology (Oxford). 2022 Nov 28;61(12):4875-4884. doi: 10.1093/rheumatology/keac165.

Abstract

OBJECTIVE

MCTD manifests with microvasculopathy and overlapping clinical features of SLE, SSc and idiopathic inflammatory myopathies (IIM). The aim of this study was to investigate the clinical significance of microvasculopathy in patients with MCTD using nailfold videocapillaroscopy (NVC).

METHODS

Fifty patients with newly diagnosed and untreated MCTD were enrolled in this multicentre, prospective and observational study. Clinical features and NVC findings were assessed at baseline and after 1 year post-intervention, along with disease controls [SLE (n = 40), SSc (n = 70) and IIM (n = 50)].

RESULTS

All MCTD patients presented Raynaud's phenomenon and were positive for anti-U1 RNP antibodies, and 22.0% (11/50) had pulmonary arterial hypertension (PAH). The prevalence of NVC scleroderma patterns in MCTD was 38.0%, which was lower than SSc (88.6%) but higher than SLE (10.0%). In addition, when we divided MCTD patients into two groups by presence or absence of NVC scleroderma patterns, we found a higher prevalence of PAH in patients with NVC scleroderma patterns. Namely, NVC scleroderma patterns were observed in all MCTD patients with PAH, and in 21.0% of those without PAH. After intensive immunosuppressive therapy, NVC scleroderma patterns disappeared in half of the MCTD patients but were not changed in SSc patients.

CONCLUSIONS

MCTD differed from SLE, SSc and IIM in terms of the prevalence and responsiveness of NVC scleroderma patterns to immunosuppressive therapy. Detection of nailfold microvascular abnormalities in MCTD could contribute to predicting PAH and help us to understand further aspects of the pathogenesis of MCTD.

摘要

目的

混合性结缔组织病(MCTD)表现为微血管病变以及系统性红斑狼疮(SLE)、系统性硬化症(SSc)和特发性炎性肌病(IIM)的重叠临床特征。本研究旨在使用甲襞视频毛细血管显微镜检查(NVC)来研究微血管病变在MCTD患者中的临床意义。

方法

50例新诊断且未治疗的MCTD患者被纳入这项多中心、前瞻性观察研究。在基线和干预后1年评估临床特征和NVC检查结果,同时纳入疾病对照 [SLE(n = 40)、SSc(n = 70)和IIM(n = 50)]。

结果

所有MCTD患者均出现雷诺现象且抗U1 RNP抗体呈阳性,22.0%(11/50)患有肺动脉高压(PAH)。MCTD中NVC硬皮病样表现的患病率为38.0%,低于SSc(88.6%)但高于SLE(10.0%)。此外,当我们根据是否存在NVC硬皮病样表现将MCTD患者分为两组时,我们发现有NVC硬皮病样表现的患者中PAH患病率更高。具体而言,所有患有PAH的MCTD患者均观察到NVC硬皮病样表现,而在无PAH的患者中有21.0%观察到该表现。经过强化免疫抑制治疗后,一半的MCTD患者NVC硬皮病样表现消失,但SSc患者未发生变化。

结论

MCTD在NVC硬皮病样表现的患病率以及对免疫抑制治疗的反应性方面与SLE、SSc和IIM不同。检测MCTD中甲襞微血管异常有助于预测PAH,并有助于我们进一步了解MCTD的发病机制。

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