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本文引用的文献

1
Growth differentiation factor 15 contributes to marrow adipocyte remodeling in response to the growth of leukemic cells.生长分化因子 15 有助于骨髓脂肪细胞重塑以响应白血病细胞的生长。
J Exp Clin Cancer Res. 2018 Mar 22;37(1):66. doi: 10.1186/s13046-018-0738-y.
2
Interpretation of clinical endpoints in trials of acute myeloid leukemia.急性髓系白血病试验中临床终点的解读
Leuk Res. 2018 May;68:32-39. doi: 10.1016/j.leukres.2018.02.002. Epub 2018 Feb 7.
3
Growth Differentiation Factor-15 Is a Predictor of Mortality in Critically Ill Patients with Sepsis.生长分化因子 15 是脓毒症危重症患者死亡率的预测因子。
Dis Markers. 2017;2017:5271203. doi: 10.1155/2017/5271203. Epub 2017 Oct 18.
4
Growth differentiation factor (GDF-15) concentration combined with Ca125 levels in serum is superior to commonly used cancer biomarkers in differentiation of pancreatic mass.生长分化因子 15(GDF-15)浓度联合血清 CA125 水平在胰腺肿块鉴别诊断中优于常用的肿瘤标志物。
Cancer Biomark. 2018 Feb 14;21(3):505-511. doi: 10.3233/CBM-170203.
5
Stromal Growth Differentiation Factor 15 and Its Association with Ovarian Cancer.基质生长分化因子15及其与卵巢癌的关联。
Gynecol Obstet Invest. 2018;83(1):35-39. doi: 10.1159/000473891. Epub 2017 May 12.
6
Growth differentiation factor 15 contributes to cancer-associated fibroblasts-mediated chemo-protection of AML cells.生长分化因子15有助于癌症相关成纤维细胞介导的急性髓系白血病细胞的化学保护作用。
J Exp Clin Cancer Res. 2016 Sep 19;35(1):147. doi: 10.1186/s13046-016-0405-0.
7
Growth differentiation factor 15 is a promising diagnostic and prognostic biomarker in colorectal cancer.生长分化因子15是结直肠癌中一种很有前景的诊断和预后生物标志物。
J Cell Mol Med. 2016 Aug;20(8):1420-6. doi: 10.1111/jcmm.12830. Epub 2016 Mar 15.
8
Acute Myeloid Leukemia: A Concise Review.急性髓系白血病:简要综述
J Clin Med. 2016 Mar 5;5(3):33. doi: 10.3390/jcm5030033.
9
Plasma growth differentiation factor 15 is associated with weight loss and mortality in cancer patients.血浆生长分化因子15与癌症患者的体重减轻和死亡率相关。
J Cachexia Sarcopenia Muscle. 2015 Dec;6(4):317-24. doi: 10.1002/jcsm.12033. Epub 2015 Apr 30.
10
Diabetes mellitus related biomarker: The predictive role of growth-differentiation factor-15.糖尿病相关生物标志物:生长分化因子-15的预测作用
Diabetes Metab Syndr. 2016 Jan-Mar;10(1 Suppl 1):S154-7. doi: 10.1016/j.dsx.2015.09.016. Epub 2015 Oct 9.

血清生长分化因子15水平对急性髓系白血病患者的预后影响

Prognostic Impact of Serum Growth Differentiation Factor 15 Level in Acute Myeloid Leukemia Patients.

作者信息

Hegab Hany Mohamed, El-Ghammaz Amro Mohamed Sedky, El-Razzaz Mostafa Kamal, Helal Reham Ali Ali

机构信息

Clinical Hematology and Bone Marrow Transplantation Unit, Internal Medicine Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

Department of Internal Medicine, Rabigh Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

出版信息

Indian J Hematol Blood Transfus. 2021 Jan;37(1):37-44. doi: 10.1007/s12288-020-01315-7. Epub 2020 Jun 30.

DOI:10.1007/s12288-020-01315-7
PMID:33707833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7900335/
Abstract

Growth differentiation factor 15 (GDF15) plays an important role in cancer pathophysiology and prognosis. However, limited studies analyzed its level and prognostic value in acute myeloid leukemia (AML) patients. This study included 56 adult AML patients. Serum GDF15 level was measured at diagnosis in all patients by enzyme-linked immunosorbent assay. Remission and survival statuses were assessed at 90 days following treatment. GDF15 level was significantly higher in patients than in controls ( < 0.001). GDF15 level correlated positively with age ( < 0.001), hemoglobin level ( = 0.027), and platelet count ( = 0.024). High GDF15 above the median level was associated with inferior OS ( = 0.044) together with high platelet count ( = 0.006) and high bone marrow blast percent ( = 0.038). There was no statistically significant difference between patients with GDF15 above and below the median level regarding DFS (P = 0.881). On multivariate analysis for OS, GDF15 level was an independent risk factor ( = 0.047). In conclusion, serum GDF15 level is significantly elevated in AML patients and high GDF15 level is associated with inferior OS.

摘要

生长分化因子15(GDF15)在癌症病理生理学和预后中发挥重要作用。然而,分析其在急性髓系白血病(AML)患者中的水平和预后价值的研究有限。本研究纳入了56例成年AML患者。所有患者在诊断时通过酶联免疫吸附测定法测量血清GDF15水平。在治疗后90天评估缓解和生存状态。患者的GDF15水平显著高于对照组(<0.001)。GDF15水平与年龄(<0.001)、血红蛋白水平(=0.027)和血小板计数(=0.024)呈正相关。高于中位数水平的高GDF15与较差的总生存期(OS)(=0.044)以及高血小板计数(=0.006)和高骨髓原始细胞百分比(=0.038)相关。GDF15高于和低于中位数水平的患者之间的无病生存期(DFS)无统计学显著差异(P=0.881)。在OS的多因素分析中,GDF15水平是一个独立危险因素(=0.047)。总之,AML患者的血清GDF15水平显著升高,高GDF15水平与较差的OS相关。