Familial Cases of Legg–Calvé–Perthes Disease—Hemostatic and Molecular Markers

Legg-Calvé-Perthes disease (LCPD) is a rare disease caused by avascular necrosis of the femoral head. Although its etiology is still not fully understood, evidence suggests that heritable prothrombotic and inflammatory factors, as well as environmental factors, may be implicated in its onset and progress. The objective of this study is to describe the genetic, biochemical, and environmental factors that may be associated with the etiology of LCPD. This study was conducted in three families and included seven related patients with an LCPD diagnosis. We evaluated the following gene alterations using real-time PCR: <i>MTHFR</i>, <i>CBS</i>, <i>COL1A1</i>, <i>COL2A1</i>, <i>PT</i>, <i>FVL</i>, <i>FVIII</i>, <i>FIX</i>, <i>PAI-1</i>, <i>eNOS</i>, <i>IL-23R</i>, <i>TNF-α</i>, <i>RANNK</i>, <i>RANNK-L</i>, <i>OPG</i> and <i>IL-6</i>. Additionally, we assessed fourteen thrombophilia-associated biochemical markers, as well as environmental factors that may be associated with the etiology of LCPD in family cases. The results show different hemostatic alterations in every individual analyzed, presenting out-of-range values in one or more parameters. Concentrations of hemoglobin and fibrinogen and the FIX activity percentage showed statistically significant differences (<i>p</i> < 0.001) when compared with healthy controls. All patients presented at least one mutated allele for the <i>MTFHR</i> (rs1801133), IL-23R (rs1569922) and <i>OPG</i> (rs2073618) polymorphisms, as well as isolated cases with other genetic variants. Our results show environmental elements from every family, and hemostatic and inflammatory disorders, may be involved in the development of LCPD. Furthermore, genetic variants could contribute to the onset of the disease. This study highlights the multifactorial nature of this pathology, involving various environmental, genetic, inflammatory, and prothrombotic factors in three families that included seven patients diagnosed with LCPD.