Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisited

Abstract

Current hemophagocytic lymphohistiocytosis 2004 (HLH-2004)-based diagnostic criteria for familial hemophagocytic lymphohistiocytosis (FHL) are based on expert opinion. Here, we performed a case-control study to test and possibly improve these criteria. We also developed 2 complementary expert opinion-based diagnostic strategies for FHL in patients with signs/symptoms suggestive of HLH, based on genetic and cellular cytotoxicity assays. The cases (N = 366) were children aged <16 years with verified familial and/or genetic FHL (n = 341) or Griscelli syndrome type 2 (n = 25); 276 from the HLH-94/HLH-2004 databases and 90 from the Italian HLH Registry. All fulfilled the HLH-94/HLH-2004 patient inclusion criteria. Controls were 374 children with systemic-onset juvenile idiopathic arthritis (sJIA) and 329 + 361 children in 2 cohorts with febrile infections that could be confused with HLH and sepsis, respectively. To provide complete data sets, multiple imputations were performed. The optimal model, based on 17 variables studied, revealed almost similar diagnostic thresholds as the existing criteria, with accuracy 99.1% (sensitivity 97.1%; specificity 99.5%); the original HLH-2004 criteria had accuracy 97.4% (sensitivity 99.0%; specificity 97.1%). Because cellular cytotoxicity assays here constitute a separate diagnostic strategy, HLH-2004 criteria without natural killer (NK)-cell function was also studied, which showed accuracy 99.0% (sensitivity, 96.2%; specificity, 99.5%). Thus, we conclude that the HLH-2004 criteria (without NK-cell function) have significant validity in their current form when tested against severe infections or sJIA. It is important to exclude underlying malignancies and atypical infections. In addition, complementary cellular and genetic diagnostic guidelines can facilitate necessary confirmation of clinical diagnosis.

Graphical abstract

Figure 1.

Presentation of all original continuous variables evaluated in cases and controls. Beeswarm panels of all original continuous variables evaluated in cases (N = 366) and the 3 control groups: hemoglobin, absolute neutrophil count, platelet count, triglycerides, fibrinogen, ferritin, sCD25, ALT, AST, LDH, bilirubin, albumin, and creatinine. These analyzed values presented do not include any imputed values. “Infection-1” includes 329 children with systemic infections that could be confused with MAS-HLH. “Infection-2” includes 361 children with severe sepsis treated at a pediatric ICU. “Rheuma” includes 374 children with systemic juvenile idiopathic arthritis, all without MAS-HLH.

Figure 1.

Presentation of all original continuous variables evaluated in cases and controls. Beeswarm panels of all original continuous variables evaluated in cases (N = 366) and the 3 control groups: hemoglobin, absolute neutrophil count, platelet count, triglycerides, fibrinogen, ferritin, sCD25, ALT, AST, LDH, bilirubin, albumin, and creatinine. These analyzed values presented do not include any imputed values. “Infection-1” includes 329 children with systemic infections that could be confused with MAS-HLH. “Infection-2” includes 361 children with severe sepsis treated at a pediatric ICU. “Rheuma” includes 374 children with systemic juvenile idiopathic arthritis, all without MAS-HLH.