Circulating plasma microRNAs in systemic sclerosis-associated pulmonary arterial hypertension

被引:15
作者
Wuttge, Dirk M. [1 ,2 ]
Carlsen, Anting L. [3 ]
Teku, Gabriel [4 ]
Wildt, Marie [1 ,2 ]
Radegran, Goran [5 ,6 ]
Vihinen, Mauno [4 ]
Heegaard, Niels H. H. [3 ,7 ,8 ]
Hesselstrand, Roger [1 ,2 ]
机构
[1] Lund Univ, Dept Clin Sci Lund, Rheumatol, SE-22185 Lund, Sweden
[2] Skane Univ Hosp, SE-22185 Lund, Sweden
[3] Statens Serum Inst, Dept Autoimmunol & Biomarkers, Copenhagen S, Denmark
[4] Lund Univ, Dept Expt Med Sci, Prot Struct Bioinformat, Lund, Sweden
[5] Lund Univ, Dept Clin Sci Lund, Cardiol, Lund, Sweden
[6] Skane Univ Hosp, Hemodynam Lab, Sect Heart Failure & Valvular Dis VO Heart & Lung, Lund, Sweden
[7] Odense Univ Hosp, Dept Clin Biochem & Pharmacol, Odense, Denmark
[8] Univ Southern Denmark, Inst Clin Res, Clin Biochem, Odense, Denmark
关键词
systemic sclerosis; pulmonary arterial hypertension; microRNA; NT-pro-Brain Natriuretic Protein; BRAIN NATRIURETIC PEPTIDE; EXPRESSION; DIAGNOSIS; CLASSIFICATION; GUIDELINES; PROFILES; SURVIVAL; HYPOXIA; CLUSTER; IMPACT;
D O I
10.1093/rheumatology/keab300
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives SSc-associated pulmonary arterial hypertension (SSc-APAH) is a late but devastating complication of SSc. Early identification of SSc-APAH may improve survival. We examined the role of circulating miRNAs in SSc-APAH. Methods Using quantitative RT-PCR the abundance of mature miRNAs in plasma was determined in 85 female patients with ACA-positive lcSSc. Twenty-two of the patients had SSc-APAH. Sixty-three SSc controls without PAH were matched for disease duration. Forty-six selected miRNA plasma levels were correlated with clinical data. Longitudinal samples were analysed from 14 SSc-APAH and 27 SSc patients. Results The disease duration was 12 years for the SSc-APAH patients and 12.7 years for the SSc controls. Plasma expression levels of 11 miRNAs were lower in patients with SSc-APAH. Four miRNAs displayed higher plasma levels in SSc-APAH patients compared with SSc controls. There was significant difference between groups for miR-20a-5p and miR-203a-3p when correcting for multiple comparisons (P = 0.002 for both). Receiver operating characteristics curve showed AUC = 0.69-0.83 for miR-21-5p and miR-20a-5p or their combination. miR-20a-5p and miR-203a-3p correlated inversely with NT-pro-Brain Natriuretic Protein levels (r = -0.42 and -0.47). Mixed effect model analysis could not identify any miRNAs as predictor of PAH development. However, miR-20a-5p plasma levels were lower in the longitudinal samples of SSc-APAH patients than in the SSc controls. Conclusions Our study links expression levels of the circulating plasma miRNAs, especially miR-20a-5p and miR-203a-3p, to the occurrence of SSc-APAH in female patients with ACA-positive lcSSc.
引用
收藏
页码:309 / 318
页数:10
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