Mazurek Marcin, Szudy-Szczyrek Aneta, Homa-Mlak Iwona, Hus Marek, Małecka-Massalska Teresa, Mlak Radosław
Department of Human Physiology of Chair of Preclinical Sciences, Medical University of Lublin, 20-080 Lublin, Poland.
Department of Haematooncology and Bone Marrow Transplantation, Medical University of Lublin, 20-080 Lublin, Poland.
Cancers (Basel). 2024 Mar 24;16(7):1263. doi: 10.3390/cancers16071263.
Multiple myeloma (MM) is a hematological neoplasm of the early precursor of B-cells. The most characteristic symptoms observed during MM include hypocalcemia, anemia, bacterial infections, and renal damage. Nutritional disorders, especially malnutrition, are noted in about 35-71% of MM patients. Interleukin 1 beta (IL-1β) is a proinflammatory cytokine responsible for muscle atrophy and lipolysis during malnutrition and cachexia. This study aimed to evaluate the usefulness of the single-nucleotide polymorphism (SNP) (rs1143634) and plasma concentration of IL-1β in the assessment of the risk of nutritional disorders and prognosis in patients with MM.
In our study, 93 patients with the de novo MM were enrolled. The real-time PCR with specific TaqMan probes method was used in genotyping. The IL-1β ELISA kit was used to determine IL-1β concentration in plasma samples.
Patients with the CC genotype, compared to the carriers of the other variants of the , demonstrated significantly higher concentrations of IL-1β in plasma (7.56 vs. 4.97 pg/mL), a significantly higher risk of cachexia (OR = 5.11), and a significantly higher risk of death (HR = 2.03). Moreover, high IL-1β plasma level was related to a significantly higher risk of cachexia (OR = 7.76); however, it was not significantly associated with progression-free survival (PFS) or overall survival (OS).
Determination of the SNP (rs1143634) and plasma concentration of IL-1β may be useful in the assessment of the risk of cachexia and prognosis in patients with MM.
多发性骨髓瘤(MM)是一种B细胞早期前体的血液肿瘤。MM患者最典型的症状包括低钙血症、贫血、细菌感染和肾损伤。约35%-71%的MM患者存在营养障碍,尤其是营养不良。白细胞介素1β(IL-1β)是一种促炎细胞因子,在营养不良和恶病质期间导致肌肉萎缩和脂肪分解。本研究旨在评估单核苷酸多态性(SNP)(rs1143634)和IL-1β血浆浓度在评估MM患者营养障碍风险和预后中的作用。
在我们的研究中,纳入了93例初发MM患者。采用特异性TaqMan探针的实时PCR方法进行基因分型。使用IL-1β ELISA试剂盒测定血浆样本中IL-1β的浓度。
与其他基因型携带者相比,CC基因型患者血浆中IL-1β浓度显著更高(7.56 vs. 4.97 pg/mL),恶病质风险显著更高(OR = 5.11),死亡风险显著更高(HR = 2.03)。此外,高IL-1β血浆水平与恶病质风险显著更高相关(OR = 7.76);然而,它与无进展生存期(PFS)或总生存期(OS)无显著关联。
测定SNP(rs1143634)和IL-1β血浆浓度可能有助于评估MM患者的恶病质风险和预后。