Diagnosis of insulin autoimmune syndrome using polyethylene glycol precipitation and gel filtration chromatography with ex vivo insulin exchange.

ContextInsulin-binding antibodies may produce severe dysglycaemia in insulin-naive patients ('insulin autoimmune syndrome' (IAS) or Hirata disease), while rendering routine insulin assays unreliable. ObjectiveTo assess the performance of clinically used insulin assays and an optimal analytical approach in the context of IAS. DesignObservational biochemical study of selected patients with hyperinsulinaemic hypoglycaemia. PatientsThree patients without diabetes with recurrent spontaneous hyperinsulinaemic hypoglycaemia and 'positive' insulin antibodies. MeasurementsA panel of clinically used insulin assays (Siemens ADVIA((R)) Centaur, Siemens Immulite((R)) 2000, DiaSorin LIAISON((R)) XL, PE AutoDELFIA((R)) and the Beckman Coulter Access((R)) 2) were used before and after plasma dilution or polyethylene glycol (PEG) precipitation. Anti-insulin IgG antibodies were measured by Isletest-IAA ELISA. Gel filtration chromatography (GFC) was undertaken with and without preincubation of plasma with exogenous insulin. ResultsDilution of IAS plasma with assay-specific buffer increased insulin recovery, supporting negative immunoassay interference by antibodies. PEG precipitation of IAS plasma decreased insulin recovery using all assays except the Immulite((R)) 2000. GFC discriminated high molecular weight and monomeric insulin, while ex vivo addition of exogenous insulin to plasma increased insulin bound to antibody, thereby improving the sensitivity of detection of insulin immunocomplexes. ConclusionsImmunoprecipitation with PEG must be used with caution in screening for insulin-antibody complexes as results are assay dependent. GFC with addition of exogenous insulin can identify significant insulin immunocomplexes with enhanced sensitivity, with attendant greater clinical utility and avoidance of radiolabelled reagents.