Laboratory parameters between multisystem inflammatory syndrome in children and Kawasaki disease

Chunling Zhou1, Yan Zhao1, Xia Wang2

  • 1Department of Pediatrics, People's Hospital of Chongqing Banan District, Chongqing, China.

Pediatric Pulmonology
|September 28, 2021
PubMed

Insights

Multisystem inflammatory syndrome in children (MIS-C) and Kawasaki disease (KD) show distinct laboratory findings. MIS-C patients exhibit lower leukocytes, lymphocytes, and platelets but higher C-reactive protein and ferritin compared to KD.

Area of Science:

  • Pediatric rheumatology
  • Infectious diseases
  • Clinical immunology

Background:

  • Multisystem inflammatory syndrome in children (MIS-C) shares clinical similarities with Kawasaki disease (KD).
  • Distinguishing MIS-C from KD is crucial for appropriate patient management and understanding disease pathogenesis.
  • Laboratory parameters offer potential biomarkers to differentiate these conditions.

Purpose of the Study:

  • To systematically review and meta-analyze laboratory parameters in MIS-C.
  • To compare laboratory findings of MIS-C with those of KD and Kawasaki disease shock syndrome (KDSS).
  • To identify key laboratory differences aiding in the diagnosis and understanding of MIS-C.

Main Methods:

  • Systematic review and meta-analysis of published studies.
  • Searched databases for laboratory parameters (hematology, inflammatory, cardiac, biochemistry) of MIS-C.
  • Included twelve studies with 3073 participants (969 MIS-C patients).

Main Results:

  • MIS-C patients had lower leukocytes, lymphocyte count, and platelet count (PLT) than KD patients.
  • MIS-C patients showed higher C-reactive protein, D-dimer, and ferritin, but similar procalcitonin and erythrocyte sedimentation rate (ESR) compared to KD.
  • Differences in cardiac markers (higher CPK in MIS-C) and biochemistry (lower albumin, sodium; higher creatinine in MIS-C) were observed.

Conclusions:

  • Laboratory parameters significantly differ between MIS-C and KD.
  • Distinct hematological and inflammatory profiles may help differentiate MIS-C from KD and KDSS.
  • Further research into these laboratory markers can aid clinical evaluation and mechanistic studies of MIS-C.