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Was Antiphospholipid Syndrome a Risk Factor of Stroke? A Systemic Review and Meta-Analysis of Cohort Studies
Insights
Antiphospholipid syndrome (APS) significantly increases stroke risk. This risk is particularly high for APS patients who also have other autoimmune diseases, highlighting a critical connection.
Area of Science:
- Medical Science
- Clinical Research
- Epidemiology
Background:
- Antiphospholipid syndrome (APS) is a condition primarily defined by recurrent thrombotic events.
- The potential link between APS and an increased risk of stroke requires further investigation.
Purpose of the Study:
- To systematically review and meta-analyze existing cohort studies to verify if APS is associated with a higher risk of stroke.
- To quantify the risk of stroke in patients diagnosed with Antiphospholipid syndrome.
Main Methods:
- A comprehensive literature search was conducted across PubMed, Embase, and Cochrane databases.
- Seventeen high-quality cohort studies were included, with quality assessed using the Newcastle-Ottawa Quality Assessment Scale.
- Random-effects modeling was employed for meta-analysis, with heterogeneity assessed using I-squared statistics and publication bias evaluated via funnel plots.
Main Results:
- The pooled hazard ratio for stroke occurrence in APS patients was 1.76 (95% CI: 1.39-2.21), indicating a significantly increased risk.
- Low heterogeneity and stable results from sensitivity analyses support the robustness of the findings.
- Subgroup analysis revealed a pooled risk ratio of 14.70 (95% CI: 7.56-28.56) for stroke in APS patients with co-existing autoimmune diseases, compared to 1.75 (95% CI: 0.99-3.09) for those with only positive antibodies.
Conclusions:
- Antiphospholipid syndrome is identified as a potential risk factor for stroke.
- The risk of stroke is substantially elevated in APS patients, especially when accompanied by other autoimmune conditions.
Abstract:
Antiphospholipid syndrome (APS) is characterized by thrombosis. This systemic review and meta-analysis was to verify the hypothesis that APS might increase the risk of stroke. Studies were identified after literature searching of PubMed, Embase, and Cochrane. Newcastle-Ottawa Quality Assessment Scale Cohort Studies (NOQAS-C) was used to assess the quality of studies. The pooled effect with 95% confidence interval (95% CI) was calculated by random-effect model. I-square (I 2) was used to test heterogeneity. Funnel plot was used to evaluate publication bias. A total of 17 cohort studies with overall high quality were included. There was no publication bias. Pooled hazard ratio of stroke occurrence in APS patients was 1.76 (1.39-2.21) with low heterogenicity and stable result from sensitivity analysis. In the analysis of subgroups, pooled risk ratios of stroke occurrence in patients with only positive antibodies of APS diagnosis were 1.75 (0.99-3.09), which for the APS patients with other autoimmune diseases were 14.70 (7.56-28.56). APS might be a risk factor of stroke, especially in patients with other autoimmune diseases.
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