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Diagnostic accuracy of alternative biomarkers for acute aortic syndrome: a systematic review
Joshua Wren1, Steve Goodacre2, Abdullah Pandor3
1Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Insights
Current guidelines recommend D-dimer for acute aortic syndrome (AAS). This review found few alternative biomarkers with consistent accuracy, indicating they are not yet ready for clinical use in AAS diagnosis.
Area of Science:
- Emergency Medicine
- Cardiovascular Diagnostics
- Biomarker Research
Background:
- D-dimer is the sole recommended biomarker for diagnosing acute aortic syndrome (AAS).
- This systematic review aimed to identify and evaluate alternative biomarkers for AAS diagnosis.
- Investigating novel diagnostic markers is crucial for improving patient outcomes.
Approach:
- Systematic review of electronic databases (MEDLINE, EMBASE, Cochrane Library) up to February 2024.
- Included diagnostic cohort studies examining biomarkers other than D-dimer for AAS.
- Excluded case-control studies due to high risk of bias; assessed quality using QUADAS-2 tool.
Key Points:
- 13 cohort studies were included, with variable methodological quality and risk of bias.
- Only two studies reported biomarkers with sensitivity and specificity comparable to D-dimer.
- Soluble ST2 and neutrophil count showed potential but lacked consistent validation across studies.
Conclusions:
- Numerous potential alternative biomarkers for AAS exist.
- Few have been evaluated in multiple studies, and study designs are often weak.
- Current alternative biomarkers are not sufficiently accurate or consistent for routine clinical use in AAS diagnosis.
Background:
D-dimer is the only biomarker currently recommended in guidelines for the diagnosis of acute aortic syndrome (AAS). We undertook a systematic review to determine whether any alternative biomarkers could be useful in AAS diagnosis.
Methods:
We searched electronic databases (including MEDLINE, EMBASE and the Cochrane Library) from inception to February 2024. Diagnostic studies were eligible if they examined biomarkers other than D-dimer for diagnosing AAS compared with a reference standard test in people presenting to the ED with symptoms of AAS. Case-control studies were identified but excluded due to high risk of bias. Selection of studies, data extraction and risk of bias assessments using the Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2) tool were undertaken independently by at least two reviewers. We used narrative synthesis to summarise the findings.
Results:
We identified 2017 citations, included 13 cohort studies (n=76-999), and excluded 38 case-control studies. Methodological quality was variable, with most included studies having unclear or high risk of bias and applicability concerns in at least one item of the QUADAS-2 tool. Only two studies reported biomarkers with sensitivity and specificity comparable to D-dimer (ie, >90% and >50%, respectively). Wang et al reported 99.1% sensitivity and 84.9% specificity for soluble ST2; however, these findings conflicted with estimates of 58% sensitivity and 70.8% specificity reported in another study. Chun and Siu reported 95.6% sensitivity and 56.1% specificity for neutrophil count, but this has not been confirmed elsewhere.
Conclusion:
There are many potential alternative biomarkers for AAS but few have been evaluated in more than one study, study designs are often weak and reported biomarker accuracy is modest or inconsistent between studies. Alternative biomarkers to D-dimer are not ready for routine clinical use.
Prospero Registration Number:
CRD42022252121.
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