Thrombosis risk with haemoglobin C trait and haemoglobin C disease: A systematic review

Author:

Jacobs Jeremy W.1ORCID,Sharma Deva23ORCID,Stephens Laura D.4ORCID,Figueroa Villalba Cristina A.5,Rinder Henry M.56ORCID,Woo Jennifer S.7,Wheeler Allison P.89ORCID,Gerberi Dana10,Goel Ruchika111213ORCID,Tormey Christopher A.5ORCID,Booth Garrett S.2ORCID,Bloch Evan M.13ORCID,Adkins Brian D.14ORCID

Affiliation:

1. Special Coagulation Laboratory, Division of Hematopathology, Department of Laboratory Medicine and Pathology Mayo Clinic Rochester Minnesota USA

2. Division of Transfusion Medicine, Department of Pathology, Microbiology, and Immunology Vanderbilt University Medical Center Nashville Tennessee USA

3. Division of Hematology/Oncology, Department of Medicine, Vanderbilt‐Meharry Center for Excellence in Sickle Cell Disease Vanderbilt University Medical Center Nashville Tennessee USA

4. Department of Pathology University of California San Diego La Jolla California USA

5. Department of Laboratory Medicine Yale School of Medicine New Haven Connecticut USA

6. Department of Hematology Yale School of Medicine New Haven Connecticut USA

7. Department of Pathology City of Hope National Medical Center Irvine California USA

8. Division of Coagulation Medicine, Department of Pathology, Microbiology, and Immunology Vanderbilt University Medical Center Nashville Tennessee USA

9. Division of Hematology/Oncology, Department of Pediatrics Vanderbilt University Medical Center Nashville Tennessee USA

10. Mayo Clinic Libraries, Mayo Clinic Rochester Minnesota USA

11. Department of Internal Medicine Simmons Cancer Institute, Southern Illinois University School of Medicine Springfield Illinois USA

12. Vitalant, Corporate Medical Affairs Scottsdale Arizona USA

13. Department of Pathology Johns Hopkins University School of Medicine Baltimore Maryland USA

14. Department of Pathology University of Texas Southwestern Medical Center Dallas Texas USA

Abstract

SummaryThe thrombotic risk with haemoglobin C trait (HbAC) or haemoglobin C disease (HbCC) is unclear. However, individuals with HbCC have demonstrated chronic haemolysis, higher blood viscosity and altered rheology when compared to individuals with wild‐type haemoglobin (HbAA). These physiological alterations may theoretically translate to increased risk of thrombosis; therefore, a systematic literature review was performed to investigate the possible association between HbAC and/or HbCC and thrombosis. Twenty‐two studies met inclusion criteria representing 782 individuals with HbAC (n = 694) or HbCC (n = 88). Fifteen studies described the presence/absence of venous thromboembolism (VTE) in patients with HbAC (n = 685) or HbCC (n = 79), while seven studies described patients with HbAC (n = 9) or HbCC (n = 9) and arterial thrombosis. Most (n = 20) studies were case reports or case series; however, two studies suggested a potential increased VTE risk with HbAC compared to HbAA in (i) all patients (OR 2.2, 95% CI: 0.9–5.5) and in (ii) pregnant individuals (RR 3.7, 95% CI 0.9–16). This review is the largest assessment of patients with HbC trait or disease and thrombosis to date; despite its limitations, the findings suggest HbC may be a predisposing risk factor to thrombosis. Prospective cohort studies are warranted to definitively elucidate the risk of thrombosis in this population.

Publisher

Wiley

Subject

Hematology

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