Vascular endothelial injury assessed with functional techniques in systemic sclerosis patients with pulmonary arterial hypertension versus systemic sclerosis patients without pulmonary arterial hypertension: a systematic review and meta-analysis
Abstract Microvascular dysfunction is one of the hallmarks of systemic sclerosis (SSc). The presence of pulmonary-arterial-hypertension (PAH) in SSc-patients is associated with poor prognosis. This is a systematic review and meta-analysis of studies assessing microvascular and endothelial injury with functional techniques in SSc-patients with PAH (SSc–PAH) compared to those without PAH (SSc–non-PAH) (PROSPERO: CRD42021236212). Literature search involved PubMed, the-Cochrane-Library, Web-of-Science, Scopus and manual search of article references. Studies assessing microvascular function by all available functional methods were considered eligible. Preclinical studies and studies using structural nailfold-videocapillaroscopy or biomarkers were excluded. Newcastle–Ottawa-Scale (NOS) was applied to evaluate the quality of retrieved studies. From a total of 602 retrieved articles, four studies (n = 159 participants) were included in meta-analysis; three studies were of high quality (NOS ≥ 7). In pooled analysis, a marginally significant impaired microvascular function was observed in SSc–PAH compared to SSc–non-PAH patients [SMD − 0.71, 95% CI (− 1.53, 0.12)], with significant between-study heterogeneity (I2 = 80%, p = 0.002). Among the studies examining endothelium-dependent and -independent vasodilation with LDF-iontophoresis, SSc–PAH subjects had significantly impaired endothelium-dependent-vasodilation [Ach-stimulated %change WMD − 216.79, 95% CI (− 337.87, − 95.71), I2 = 0%, p = 0.40], but no significant differences in endothelium-independent-vasodilation [SNP-stimulated %change WMD 90.84, 95% CI (− 82.52, 264.19), I2 = 44%, p = 0.18] compared with SSc–non-PAH subjects. In sensitivity analysis including only studies where SSc–PAH patients were diagnosed by right-heart-catheterization, a borderline difference between the two groups was noted [SMD − 1.09, 95% CI (− 2.30, 0.13), I2 = 82%, p = 0.004]. SSc–PAH patients showed marginally impaired microvascular function in the pooled analysis, as well as impaired endothelium-dependent-vasodilation in subgroup analysis compared with SSc–non-PAH patients. Vascular endothelial dysfunction could be involved in high cardiovascular risk of patients with SSc and PAH..
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Artikel |
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Erscheinungsjahr: |
2021 |
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Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:41 |
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Enthalten in: |
Rheumatology international - 41(2021), 6 vom: 08. Apr., Seite 1045-1053 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Theodorakopoulou, Marieta P. [VerfasserIn] |
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Links: |
Volltext [lizenzpflichtig] |
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Themen: |
Endothelial dysfunction |
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Anmerkungen: |
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 |
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doi: |
10.1007/s00296-021-04850-2 |
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funding: |
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PPN (Katalog-ID): |
OLC212515112X |
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520 | |a Abstract Microvascular dysfunction is one of the hallmarks of systemic sclerosis (SSc). The presence of pulmonary-arterial-hypertension (PAH) in SSc-patients is associated with poor prognosis. This is a systematic review and meta-analysis of studies assessing microvascular and endothelial injury with functional techniques in SSc-patients with PAH (SSc–PAH) compared to those without PAH (SSc–non-PAH) (PROSPERO: CRD42021236212). Literature search involved PubMed, the-Cochrane-Library, Web-of-Science, Scopus and manual search of article references. Studies assessing microvascular function by all available functional methods were considered eligible. Preclinical studies and studies using structural nailfold-videocapillaroscopy or biomarkers were excluded. Newcastle–Ottawa-Scale (NOS) was applied to evaluate the quality of retrieved studies. From a total of 602 retrieved articles, four studies (n = 159 participants) were included in meta-analysis; three studies were of high quality (NOS ≥ 7). In pooled analysis, a marginally significant impaired microvascular function was observed in SSc–PAH compared to SSc–non-PAH patients [SMD − 0.71, 95% CI (− 1.53, 0.12)], with significant between-study heterogeneity (I2 = 80%, p = 0.002). Among the studies examining endothelium-dependent and -independent vasodilation with LDF-iontophoresis, SSc–PAH subjects had significantly impaired endothelium-dependent-vasodilation [Ach-stimulated %change WMD − 216.79, 95% CI (− 337.87, − 95.71), I2 = 0%, p = 0.40], but no significant differences in endothelium-independent-vasodilation [SNP-stimulated %change WMD 90.84, 95% CI (− 82.52, 264.19), I2 = 44%, p = 0.18] compared with SSc–non-PAH subjects. In sensitivity analysis including only studies where SSc–PAH patients were diagnosed by right-heart-catheterization, a borderline difference between the two groups was noted [SMD − 1.09, 95% CI (− 2.30, 0.13), I2 = 82%, p = 0.004]. SSc–PAH patients showed marginally impaired microvascular function in the pooled analysis, as well as impaired endothelium-dependent-vasodilation in subgroup analysis compared with SSc–non-PAH patients. Vascular endothelial dysfunction could be involved in high cardiovascular risk of patients with SSc and PAH. | ||
650 | 4 | |a Pulmonary arterial hypertension | |
650 | 4 | |a Systemic sclerosis | |
650 | 4 | |a Endothelial dysfunction | |
650 | 4 | |a Functional methods | |
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