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Published on: January 18, 2020
Cryoglobulins: an important but neglected clinical test
1Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA. zshihabi@wfubmc.edu
Insights
Cryoglobulin (CR) testing is underutilized despite its importance in managing vasculitis. Low CR levels, often missed, can indicate severe conditions, necessitating faster, reliable detection methods.
Area of Science:
- Immunology
- Clinical Chemistry
Background:
- Cryoglobulins (CR) are immunoglobulins precipitating below 37°C, crucial in diagnosing autoimmune and infectious disorders like Hepatitis C Virus (HCV).
- CR measurement is vital for managing vasculitis, though often neglected in routine practice due to complex analysis and underappreciation of low-level CR significance.
Observation:
- CRs are heterogeneous immune complexes, presenting with varied symptoms from purpura to severe nephropathy and neuropathy.
- A study of 194 positive CR samples revealed the majority had low concentrations (Type II mean 372 mg/L, Type III mean 216 mg/L; reference range 0-60 mg/L).
Findings:
- Low CR concentrations, frequently observed, are associated with significant clinical manifestations, including severe conditions.
- Current CR testing methods are time-consuming and may fail to detect clinically relevant low-level CR.
Implications:
- There is a critical need for improved, rapid, and reliable methods for quantifying and phenotyping low serum CR concentrations.
- Enhanced CR detection and characterization can improve patient management, particularly in HCV-associated vasculitis and autoimmune diseases.
Abstract:
Cryoglobulin (CR) denotes a serum immunoglobulin that precipitates at temperatures below 37 degrees C and dissolves on re-warming. CRs are heterogeneous in chemical composition and behave differently in vivo and in vitro. The majority are mixed antigen-antibody complexes that occur with high incidence in autoimmune and infectious disorders. Their measurement is important in the management of patients with vasculitis. CRs elicit variable symptoms in patients, mostly purpura, weakness, and arthralgias, and they require various methods of treatment. Sometimes CRs are not associated with any symptoms; but they can be associated with very severe conditions such as nephropathy and neuropathy. Treatment depends on the symptoms and causes, and on the phenotyping of the CR. Considering the high incidence of CR in diseases such as hepatitis C virus (HCV) infection, together with the high worldwide prevalence of this disease, it is clear that testing for CR is underutilized in clinical practice. CR testing has been neglected in routine clinical laboratories and by clinicians due to several factors, such as the lengthy time for serum CR analysis and failure to appreciate that low levels of CR can be associated with severe symptoms. In a series of 194 serum samples that gave positive tests for CR at our institution, the majority contained low CR concentrations (65% of the samples were type II with a mean of 372 mg/L and 39% of type III with a mean of 216 mg/L; reference range 0-60 mg/L). Case studies are presented to illustrate the importance of such low levels of CR. There is a need for more rapid and more reliable methods for quantification and phenotyping of low concentrations of serum CR. Based on our experience in the routine analysis, quantification, and phenotyping of serum CR, some practical solutions to these problems are presented.
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