Diagnostic and Treatment of Cryoglobulinemiс Vasculitis: What is Important for Real Clinical Practice?

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І. Ю. Головач
Є. Д. Єгудіна

Abstract

Cryoglobulinemia is a condition in which circulating cryoprecipitate immune complexes are detected in serum. The cryoglobulin concentration above 50 mg/l is considered diagnostically significant for the statement of cryoglobulinemia. The production of cryoglobulins, as a rule, is a consequence of the underlying disease, which requires etiological evaluation. The diagnosis of cryoglobulinemic vasculitis (CV) is based on laboratory detection of serum cryoglobulinemia in combination with characteristic clinical signs and symptoms. The main clinical manifestations include common symptoms (severe fatigue, unexplained fever with or without weight loss), skin lesions (orthostatic palpable purpura, necrotic ulcers), joints (arthritis, arthralgia), peripheral nervous system (mononeuritis, polyneuritis) and kidney (membranoproliferative glomerulonephritis). Given the many signs and symptoms, a patient with CV rarely turns primarily to a rheumatologist. First contact doctors are often family doctors or dermatologists, along with the fact that the awareness of doctors of other specialties about this pathology is insufficient. The article presents modern data on the etiological factors, CV types and variants of the clinical course and treatment. CV classification criteria are highly informative and available to practitioners. Treatment of CV remains a challenge due to serious specific target organ damage and sometimes life-threatening manifestations. In secondary cryoglobulinemia, treatment of the underlying disease is crucial. In case of CV on the background of mixed cryoglobulinemia, the treatment strategy is based on antiviral, anti-inflammatory and immunosuppressive therapy. The therapy goals for CV include reducing the immunoglobulin level and removing the antigen. The first goal can be achieved with immunosuppressants, while the second goal depends on whether the antigen is known or not. With CV associated with HCV, antiviral therapy reduces the number of antigens. However, in autoimmune diseases, the potential antigen is usually not recognized, and only non-specific immunosuppressants are used.

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How to Cite
Головач, І. Ю., & Єгудіна, Є. Д. (2019). Diagnostic and Treatment of Cryoglobulinemiс Vasculitis: What is Important for Real Clinical Practice?. Family Medicine, (4), 20–29. https://doi.org/10.30841/2307-5112.4.2019.184366
Section
Topical issues
Author Biographies

І. Ю. Головач, Feofaniya Clinical Hospital of State Management of Affairs of Ukraine

Iryna Yu. Golovach,

Head of the Center of Reumatology

Є. Д. Єгудіна, State Establishment «Dnipropetrovsk Medical Academy of Health Ministry of Ukraine»

Yelizaveta D. Yehudina,

Department of Internal Medicine 3

References

Anis S, Abbas K, Mubarak M, Ahmed E, Bhatti S, Muzaffar R. Vasculitis with renal involvement in essential mixed cryoglobulinemia: Case report and mini-review. World J Clin Cases. 2014; 2(5):160–166. doi: 10.12998/wjcc.v2.i5.160

Artishevskaia NI, Rayeuneva TG, Savtshenco MA, et al. Сryoglobulinemic vasculitis in clinic of internal disease. Medical journal. 2018;3:4-9.

Befort P, Corne P, Filleron T, et al. Prognosis and ICU outcome of systemic vasculitis. BMC Anesthesiol. 2013;13: 27. doi: 10.1186/1471-2253-13-27

Brito-Zerón P, Baldini C, Bootsma H, et al. Sjögren syndrome. Nat. Rev. Dis. Primers. 2016;7(2):16047. doi: 10.1038/nrdp.2016.47

Cacoub P, Comarmond C, Domont F, Savey L, Saadoun D. Cryoglobulinemia Vasculitis. Am J Med. 2015;128(9):950 http://dx.doi.org/10.1016/j. amjmed.2015.02.017

De Sanjose S, Benavente Y, Vajdic CM, et al. Hepatitis C and non- Hodgkin lymphoma among 4784 cases and 6269 controls from the International Lymphoma Epidemiology Consortium. Clin. Gastroenterol. Hepatol. 2008;6(4):451–458. doi: 10.1016/j.cgh.2008.02.011

De Vita S, Soldano F, Isola M, et al. Preliminary classification criteria for the cryoglobulinaemic vasculitis. Ann. Rheum. Dis. 2011;70:1183–1190 doi: 10.1136/ard.2011.150755.

Desbois AC, Cacoub P, Saadoun D. Cryoglobulinemia: An update in 2019. Joint Bone Spine, 2019;4:S1297-319X. doi: 10.1016/j.jbspin.2019.01.01

Feldman L, Dhamne M, Li Y. Neurologic manifestations associated with cryoglobulinemia: A single center experience. J Neurol Sci. 2019; 398:121-127. doi: 10.1016/j.jns.2019.01.041.

Ferri C, Antonelli A, Mascia MT, et al. B cells and mixed cryoglobulinemia. Autoimmun. Rev. 2007; 7(2):114–120. DOI:10.1016/j.autrev.2007.02.019

Ferri C, Sebastiani M, Giuggioli D, et al. Hepatitis C virus syndrome: a constellation of organ- and non- organ specific autoimmune disorders, B cell non- Hodgkin’s lymphoma, and cancer. World J. Hepatol. 2015; 7(3): 327–343 doi: 10.4254/wjh.v7.i3.327.

Ferri C, Ramos-Casals M, Zignego AL, et al. International diagnostic guidelines for patients with HCV- related extrahepatic manifestations. A multidisciplinary expert statement. Autoimmun. Rev. 2016; 15(12): 1145–1160. doi: 10.1016/j.autrev.2016.09.006.

Galli M, Oreni L, Saccardo F, et al. HCVunrelated cryoglobulinaemic vasculitis: the results of a prospective observational study by the Italian Group for the Study of Cryoglobulinaemias (GISC). Clin. Exp. Rheumatol. 2017; 35 (Suppl. 1):67–76.

Hiramatsu R, Hoshino J, Suwabe T, et al. Membranoproliferative glomerulonephritis and circulating cryoglobulins. Clin Exp Nephrol. 2014;18(1):88-94. doi: 10.1007/s10157-013-0810-z.

Ignatova TM, Kozlovskaya LV, Gordovskaya NB, et al. Hepatitis C virusassociated cryoglobulinemic vasculitis: A 20-year experience with treatment. Ter Arkh. 2017;89(5):46-52. doi: 10.17116/terarkh201789546-52.

Jennette J, Falk RJ, Bacon PA, et al. 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum. 2013;65(1):1–11 doi:10.1002/art.37715

Karimifar M, Pourajam S, Tahmasebi A, Mottaghi P. Serum cryoglobulins and disease activity in systematic lupus erythematosus. J Res Med Sci, 2013;18(3): 234–238

Khaled H, Abu-Taleb F, Haggag R. Hepatitis C virus and non-Hodgkin’s lymphomas: A minireview. J Adv Res. 2017;8(2): 131–137. doi: 10.1016/j.jare.2016.11.005

Mahale P, Engels EA, Li R. The effect of sustained virological response on the risk of extrahepatic manifestations of hepatitis C virus infection. Gut. 2018; 67:553–561. doi: 10.1136/gutjnl-2017-313983

Mazzaro C, Dal Maso L, Urraro T, et al. Hepatitis B virus related cryoglobulinemic vasculitis: A multicentre open label study from the Gruppo Italiano di Studio delle Crioglobulinemie - GISC. Dig Liver Dis, 2016;48(7):780-4. doi: 10.1016/j.dld.2016.03.018

Mazzaro C, Maso LD, Mauro E, et al. Survival and Prognostic Factors in Mixed Cryoglobulinemia: Data from 246 Cases.Diseases. 2018;6(2): 35. doi: 10.3390/diseases6020035.

Minopetrou M, Hadziyannis E, Deutsch M, et al. Hepatitis C Virus (HCV)-Related Cryoglobulinemia: Cryoglobulin Type and Anti-HCV Profile. Clin Vaccine Immunol. 2013;20(5):698–703. doi: 10.1128/CVI.00720-12

Monti G, Saccardo F, Castelnovo L, et al. Prevalence of mixed cryoglobulinaemia syndrome and circulating cryoglobulins in a population- based survey: the Origgio study. Autoimmun. Rev. 2014; 13(6): 609–614. doi: 10.1016/j.autrev.2013.11.005

Néel A, Perrin F, Decaux O, et al. Long- term outcome of monoclonal (type 1) cryoglobulinemia. Am. J. Hematol. 2014;89(2);156–161. doi: 10.1002/ajh.23608

Quartuccio L, Isola M, Corazza L, et al. Validation of the classification criteria for cryoglobulinaemic vasculitis. Rheumatology. 2014;53(12):2209–2213. doi: 10.1093/rheumatology/keu271

Quartuccio L, Zuliani F, Corazza L, et al. Retreatment regimen of rituximab monotherapy given at the relapse of severe HCV-related cryoglobulinemic vasculitis: long- term follow up data of a randomized controlled multicentre study. J. Autoimmun., 2015; 63:88–93. doi: 10.1016/j.jaut.2015.07.012.

Ramos-Casals M, Stone JH, Cid, MC, et al. The cryoglobulinaemias. Lancet. 2012;379(9813):348–360. doi: 10.1016/S0140-6736(11)60242-0

Retamozo S, Díaz-Lagares C, Bosch X, et al. Life-Threatening Cryoglobulinemic Patients With Hepatitis C: Clinical Description and Outcome of 279 Patients. Medicine (Baltimore). 2013; 92(5):273-284. doi: 10.1097/MD.0b013e3182a5cf71.

Retamozo S, Brito- Zerón P, Bosch X, Stone JH, Ramos-Casals M. Cryoglobulinemic disease. Oncology (Williston Park). 2013; 27:1098–1105, 1110–1116.

Retamozo S, Gheitasi H, Quartuccio L, et al. Cryoglobulinaemic vasculitis at diagnosis predicts mortality in primary Sjögren syndrome: analysis of 515 patients. Rheumatology (Oxford). 2016; 55(8):1443–1451 doi: 10.1093/rheumatology/kew194

Retamozo S, Brito-Zerón P, Quartuccio L, De Vita S, Ramos-Casals M. Introducing treat-to-target strategies of autoimmune extrahepatic manifestations of chronic hepatitis C virus infection. Expert Rev. Clin. Pharmacol. 2017; 10:1085–1101 doi: 10.1080/17512433.2017.1357466

Roccatello D, Sciascia S, Rossi D, et al. The challenge of treating hepatitis C virus- associated cryoglobulinemic vasculitis in the era of anti-CD20 monoclonal antibodies and direct antiviral agents. Oncotarget, 2017; 8 (25): 41764–41777 doi: 10.18632/oncotarget.16986

Roccatello D, Saadoun D, Ramos-Casals M, et al. Cryoglobulinaemia. Nature reviews. 2018; 4(1):11. https://doi.org/10.1038/s41572-018-0009-4

Rogalska-Płońska M, Lapinski TW, Grzeszczuk A, Parfieniuk-Kowerda A, Flisiak R. Influence of HCV and HIV on development of cryoglobulinemia. Viral Immunol. 2015; 28(3):145-52. doi: 10.1089/vim.2014.0114

Saadoun D, Thibault V, Si Ahmed SN, et al. Sofosbuvir plus ribavirin for hepatitis C virus-associated cryoglobulinaemia vasculitis: VASCUVALDIC study. Ann Rheum Dis. 2016; 75(10):1777-82. doi: 10.1136/annrheumdis-2015-208339

Shi XH, Ma J, Li C, et al. Clinical features of 30 patients with cryoglobulinemia. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2014;36(6):639-44. doi: 10.3881/j.issn.1000-503X.2014.06.015.

Sidana S, Rajkumar SV, Dispenzieri A, et al. Clinical presentation and monoclonal cryoglobulinemia. Am J Hematol. 2017;92: 668–73, http://dx.doi.org/10.1002/ajh.24745.

Soyyigita S, Sozenera ZC, Atillab E, Heperc AO, Kaygusuzc G, Sina BA. Cold Urticaria: A Rare Manifestation of Lymphoma. Journal of Medical Cases. 2015; 6(1): 40-42. doi: http://dx.doi.org/10.14740/jmc1803w

Strait RT, Posgai MT, Mahler A, et al. IgG1 protects against mouse model of cryoglobulinaemia. Nature. 2015; 517:501–4, http://dx.doi.org/10.1038/nature13868

Terrier B, Karras A, Cluzel P, et al. Presentation and prognosis of cardiac involvement in hepatitis C virus-related vasculitis. Am J Cardiol. 2013; 111(2): 265-72. doi: 10.1016/j.amjcard.2012.09.028.

Terrier B, Marie I, Launay D, et al. Predictors of early relapse in patients with noninfectious mixed cryoglobulinemia vasculitis: results from the French nationwide CryoVas survey. Autoimmun. Rev. 2014; 13(6): 630–634. doi: 10.1016/j.autrev.2013.11.006.

Terrier B, Marie I, Lacraz A, et al. Non HCV-related infectious cryoglobulinemia vasculitis: results from the French nationwide CryoVas survey and systematic review of the literature. J. Autoimmun. 2015; 65: 74–81. doi: 10.1016/j.jaut.2015.08.008

Toriu N, Sawa N, Oguro M, et al. Renallimited Cryoglobulinemic Vasculitis: Two Case Reports. Intern Med., 2018; 57(13): 1879–1886. doi: 10.2169/internalmedicine.0131-17

Trejo O, Ramos-Casals M, García-Carrasco M, et al. Cryoglobulinemia: study of etiologic factors and clinical and immunologic features in 443 patients from a. single center. Medicine (Baltimore). 2001; 80: 252–262 DOI: 10.1097/00005792-200107000-00004

Zhao LJ, Chen F, Li JG, et al. Hepatitis C virus-related mixed cryoglobulinemic endocapillary proliferative glomerulonephritis and B-cell non-Hodgkin lymphoma: A case report and literature review. Eur Rev Med Pharmacol Sci. 2015;19: 3050–3055