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高密度脂蛋白(HDL)对骨髓瘤的预后有影响:HDL水平较低与无进展生存期较差相关。

High-density lipoprotein (HDL) has an impact on myeloma outcome: Lower HDL associates with worse progression-free survival.

作者信息

Erdoğan Özünal Işıl, Kılıçaslan Emrah, Elibol Tayfun, Öztürk Erman

机构信息

Division of Hematology, Department of Internal Medicine, Istanbul Medeniyet University, Prof. Dr. Süleyman Yalçın Göztepe City Hospital, Eğitim Mah., Kadıköy, 34722, Istanbul, Turkey.

Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Turkey.

出版信息

Wien Klin Wochenschr. 2024 Jul;136(13-14):398-404. doi: 10.1007/s00508-023-02239-8. Epub 2023 Jul 4.

Abstract

BACKGROUND

Multiple myeloma (MM) staging is based on beta‑2 MG, albumin, LDH levels, and the presence of chromosomal abnormalities. We aimed to evaluate the impact of high-density lipoprotein (HDL) on myeloma outcomes.

MATERIALS AND METHODS

This study included 148 individuals; 68 patients diagnosed with MM and 80 age, sex, comorbidity-matched controls. The relationship between HDL and myeloma stage and the association between HDL and progression-free survival (PFS) were analyzed.

RESULTS

Sixty-five percent of patients were male in each group. Mean HDL level was higher in the control group than myeloma group (52.6 ± 15.02 mg/dl versus 33.79 ± 12.71) (p < 0.001). According to ISS, 39 patients (57%) had advanced stage (ISS-III) disease. To assess the optimal cut-point for HDL that makes a difference in PFS, the X‑tile software program was used and in line with the created plots, the myeloma cohort was divided into two groups as HDL < 28 and ≥ 28 mg/dl. Twenty-two patients (32.4%) were in HDL < 28 group. According to the ISS, HDL < 28 group had more advanced disease than the HDL ≥ 28 group (p = 0.008). Twenty-nine patients (42.6%) progressed or died during the follow-up and 15 of these were in the HDL < 28 group. Time to progression was shorter in patients who were in the HDL < 28 group (median, 22 versus 40 months, p = 0.03). There was no statistically significant difference between these groups in terms of overall survival (p = 0.708).

CONCLUSION

Myeloma patients have lower HDL than controls and HDL < 28 mg/dl associates with advanced-stage disease and shorter PFS. Therefore, HDL can be a surrogate prognostic marker in myeloma.

摘要

背景

多发性骨髓瘤(MM)分期基于β2微球蛋白、白蛋白、乳酸脱氢酶水平以及染色体异常情况。我们旨在评估高密度脂蛋白(HDL)对骨髓瘤预后的影响。

材料与方法

本研究纳入148名个体;68例确诊为MM的患者以及80名年龄、性别、合并症相匹配的对照者。分析HDL与骨髓瘤分期之间的关系以及HDL与无进展生存期(PFS)之间的关联。

结果

每组中65%的患者为男性。对照组的平均HDL水平高于骨髓瘤组(52.6±15.02mg/dl对33.79±12.71)(p<0.001)。根据国际分期系统(ISS),39例患者(57%)患有晚期(ISS-III期)疾病。为评估对PFS有影响的HDL最佳切点,使用X-tile软件程序,并根据生成的图表,将骨髓瘤队列分为HDL<28mg/dl和≥28mg/dl两组。22例患者(32.4%)在HDL<28mg/dl组。根据ISS,HDL<28mg/dl组的疾病比HDL≥28mg/dl组更晚期(p=0.008)。29例患者(42.6%)在随访期间病情进展或死亡,其中15例在HDL<28mg/dl组。HDL<28mg/dl组患者的疾病进展时间较短(中位数,22个月对40个月,p=0.03)。两组在总生存期方面无统计学显著差异(p=0.708)。

结论

骨髓瘤患者的HDL低于对照组,HDL<28mg/dl与晚期疾病和较短的PFS相关。因此,HDL可作为骨髓瘤的替代预后标志物。

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