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哥伦比亚系统性硬化症患者肺动脉高压的相关危险因素:文献综述

Risk factors associated with pulmonary arterial hypertension in Colombian patients with systemic sclerosis: review of the literature.

作者信息

Coral-Alvarado Paola, Rojas-Villarraga Adriana, Latorre María C, Mantilla Ruben D, Restrepo José F, Pardo Aryce L, Chalem Philippe, Rondón Federico, Jáuregui Edwin, Rueda Juan C, Cañas Carlos, Hincapie María E, Pineda-Tamayo Ricardo, Alvarez Fausto, Iglesias-Gamarra Antonio, Diaz Francisco J, Anaya Juan-Manuel

机构信息

Rheumatology Unit, Universidad Nacional de Colombia, Bogota, Colombia.

出版信息

J Rheumatol. 2008 Feb;35(2):244-50. Epub 2008 Jan 15.

Abstract

OBJECTIVE

Considering the significant morbidity and mortality of pulmonary arterial hypertension (PAH) in patients with systemic sclerosis (SSc) and the lack of precise information on disease in Latin America, we investigated the clinical and laboratory characteristics associated with PAH in Colombian patients with SSc and review the literature.

METHODS

This multicenter study included patients followed at 5 rheumatology units that were systematically assessed using a pretested questionnaire on clinical and immunological variables, focusing on PAH. Conditional logistic regression was employed to assess association between PAH and specific clinical characteristics. A systematic review of the literature was performed through electronic databases.

RESULTS

Of a total of 349 patients with SSc, 61 (17%) met the criteria for PAH. Pulmonary fibrosis [adjusted odds ratio (AOR) 7.37, 95% CI 3.67-14.81, p < 0.0001], microstomia (AOR 3.3, 95% CI 1.70-6.28, p < 0.0001), gastroesophageal reflux (AOR 2.41, 95% CI 1.31-4.43, p = 0.005), dysphagia (AOR 2.7, 95% CI 1.49-4.77, p = 0.001), hyperpigmentation (AOR 2.15, 95% CI 1.11-4.16, p = 0.02), and hypopigmentation (AOR 2.4, 95% CI 1.26-4.64, p = 0.008) were the most prevalent clinical characteristics associated with PAH, while anemia (AOR 5.4, 95% CI 1.98-14.93, p = 0.001) was observed as the unique laboratory risk factor. Association between subtypes of SSc and PAH was not observed. Significant differences in both clinical and laboratory data were observed among different series.

CONCLUSION

PAH may be a frequent complication of SSc in the Colombian population regardless of disease subtype. The identified clinical and laboratory risk factors might assist earlier diagnosis and guide decisions on therapeutic interventions on this critical complication of SSc. The reasons underlying the reported divergences among patients from different ethnicities are not fully understood, but it is most likely that both genetic and environmental factors are responsible for them.

摘要

目的

鉴于系统性硬化症(SSc)患者中肺动脉高压(PAH)的高发病率和死亡率,以及拉丁美洲缺乏关于该疾病的确切信息,我们调查了哥伦比亚SSc患者中与PAH相关的临床和实验室特征,并对文献进行了综述。

方法

这项多中心研究纳入了在5个风湿病科接受随访的患者,使用一份经过预测试的关于临床和免疫变量的问卷进行系统评估,重点关注PAH。采用条件逻辑回归评估PAH与特定临床特征之间的关联。通过电子数据库对文献进行系统综述。

结果

在总共349例SSc患者中,61例(17%)符合PAH标准。肺纤维化[调整优势比(AOR)7.37,95%置信区间(CI)3.67 - 14.81,p < 0.0001]、小口症(AOR 3.3,95% CI 1.70 - 6.28,p < 0.0001)、胃食管反流(AOR 2.41,95% CI 1.31 - 4.43,p = 0.005)、吞咽困难(AOR 2.7,95% CI 1.49 - 4.77,p = 0.001)、色素沉着过度(AOR 2.15,95% CI 1.11 - 4.16,p = 0.02)和色素沉着不足(AOR 2.4,95% CI 1.26 - 4.64,p = 0.008)是与PAH相关的最常见临床特征,而贫血(AOR 5.4,95% CI 1.98 - 14.93,p = 0.001)是唯一观察到的实验室风险因素。未观察到SSc亚型与PAH之间的关联。不同系列之间在临床和实验室数据方面均观察到显著差异。

结论

在哥伦比亚人群中,无论疾病亚型如何,PAH可能是SSc的常见并发症。所确定的临床和实验室风险因素可能有助于早期诊断,并指导对SSc这一关键并发症的治疗干预决策。不同种族患者之间报告的差异背后的原因尚未完全理解,但很可能是遗传和环境因素共同导致的。

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