AI Article Synopsis

  • IgG4-related disease is a newly identified condition characterized by high levels of IgG4 antibodies and infiltration of IgG4+ plasma cells, which responds well to glucocorticoid treatment.
  • Researchers analyzed data from 132 patients with this disease and 48 with other conditions to establish diagnostic cutoff values for serum IgG4 levels and cell ratios in tissues.
  • The study found specific thresholds for serum IgG4 and IgG4+/IgG+ plasma cell ratios that show high sensitivity and specificity for diagnosing IgG4-related disease, but acknowledged the need for further discussion on diagnostic criteria and potential issues in severely affected tissues.

Article Abstract

IgG4-related disease is a new disease classification established in Japan in the 21st century. Patients with IgG4-related disease display hyper-IgG4-gammaglobulinemia, massive infiltration of IgG4+ plasma cells into tissue, and good response to glucocorticoids. Since IgG4 overexpression is also observed in other disorders, it is necessary to diagnose IgG4-related disease carefully and correctly. We therefore sought to determine cutoff values for serum IgG4 and IgG4/IgG and for IgG4+/IgG+ plasma cells in tissue diagnostic of IgG4-related disease. Patients and Methods. We retrospectively analyzed serum IgG4 concentrations and IgG4/IgG ratio and IgG4+/IgG+ plasma cell ratio in tissues of 132 patients with IgG4-related disease and 48 patients with other disorders. Result. Serum IgG4 >135  mg/dl demonstrated a sensitivity of 97.0% and a specificity of 79.6% in diagnosing IgG4-related disease, and serum IgG4/IgG ratios >8% had a sensitivity and specificity of 95.5% and 87.5%, respectively. IgG4+cell/IgG+ cell ratio in tissues >40% had a sensitivity and specificity of 94.4% and 85.7%, respectively. However, the number of IgG4+ cells was reduced in severely fibrotic parts of tissues. Conclusion. Although a recent unanimous consensus of all relevant researchers in Japan recently established the diagnostic criteria for IgG4-related disease, findings such as ours indicate that further discussion is needed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357966PMC
http://dx.doi.org/10.1155/2012/580814DOI Listing

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