Predictive ability of inflammatory markers and laboratory parameters in Legg-Calvé-Perthes disease: A single-center

Kenichi Mishima1, Yasunari Kamiya, Masaki Matsushita

  • 1Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan,Department of Orthopaedic Surgery, Aichi Children's Health and Medical Center, 7-426 Morioka-Cho, Obu, Aichi, Japan.

Medicine
|March 31, 2022
PubMed

Insights

Inflammatory markers like neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII) do not reliably predict Legg-Calvé-Perthes disease (LCPD) severity. Alkaline phosphatase levels may offer some insight, but overall, early disease markers are insufficient for prognosis.

Area of Science:

  • Orthopedics
  • Pediatric Orthopedics
  • Inflammatory Markers

Background:

  • Legg-Calvé-Perthes disease (LCPD) involves chronic inflammation and synovitis.
  • Currently, no definitive blood marker exists to assess LCPD severity or prognosis.
  • Neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII) indicate subclinical inflammation.

Purpose of the Study:

  • To evaluate the predictive capacity of NLR, SII, and standard laboratory tests for LCPD severity.
  • To compare these markers in LCPD patients versus age-matched controls.

Main Methods:

  • Retrospective analysis of pre-operative laboratory findings in unilateral LCPD patients undergoing Salter osteotomy and age-matched controls.
  • Data collected at osteotomy and implant removal stages.
  • Inclusion of 26-38 LCPD patients and 20 control patients.

Main Results:

  • LCPD patients showed higher mean NLR and SII, and lower alkaline phosphatase compared to controls at osteotomy.
  • Lower alkaline phosphatase levels were associated with modified lateral pillar (LP) group-A hips.
  • No significant differences in markers were found between favorable (LP-A, -B) and unfavorable (LP-B|C border, -C) hip groups.

Conclusions:

  • Early-stage inflammatory markers (NLR, SII) and common lab parameters are insufficient for predicting LCPD prognosis.
  • Alkaline phosphatase may show some correlation with LCPD hip classification.
  • Further research is needed for reliable prognostic markers in LCPD.

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