Xiao Li, Xu Ximing, Zhang Zhiling, Dou Ying, Guan Xianmin, Guo Yuxia, Yu Jie
Department of Hematology and Oncology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Chongqing Key Laboratory of Pediatrics, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Big Data Center for Children's Medical Care, Children's Hospital of Chongqing Medical University, Chongqing, China.
Front Pediatr. 2023 Jan 9;10:1006817. doi: 10.3389/fped.2022.1006817. eCollection 2022.
Hemophagocytic lymphohistiocytosis (HLH) is a rapidly progressive and potentially life-threatening disorder. Identifying risk factors and timely adjustment of the given treatment regimens is critical to reducing the early mortality in HLH patients. Hypocholesterolemia has been reported to be associated with poor prognosis in a variety of critical illnesses. However, serum cholesterol is rarely studied in HLH patients, and its prognostic value is unclear.
We conducted a retrospective cohort study in National Clinical Research Center for Child Health and Disorders (Chongqing), identifying pediatric HLH patients (including genetically confirmed pHLH and not genetically confirmed pHLH) diagnosed with the HLH-2004 protocol and treated with immunochemotherapy between January 2008 and December 2020. The patients' blood lipid levels at initial diagnosis of HLH, including triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein-cholesterol (LDL-C), were reviewed based on electronic medical records. Both Cox and logistic regression models were used to estimate the effects of blood lipid indicators on early death (within 30 days after diagnosis).
A total of 353 patients were enrolled in the study, with a median age at diagnosis of 45 months. The observed 30-day mortality rate was 19.05% (64/336, 17 were lost to follow-up) and Kaplan-Meier-estimated 3-year survival rate was 61.67% (95% CI, 56.27%-67.59%). DNA-targeted sequencing of HLH-related genes was performed in 173 (49.0%, 173/353) patients (not all patients with suspected pHLH underwent genetic testing), and 29 patients were diagnosed with genetically confirmed pHLH. Lipid panel was performed in 349 patients: 91.98% (321/349) had TG ≥ 1.80 mmol/L, 62.75%(219/349) had TG ≥ 3.00 mmol/L, 92.84% (324/349) had HDL-C ≤ 1.04 mmol/L, 58.74% (205/349) had LDL-C ≤ 1.30 mmol/L and 24.64% (86/349) had TC ≤ 3.11 mmol/L. TC ≤ 3.11 mmol/L and BUN ≥ 7.14 mmol/L were the independent risk factors for 30-day mortality [HR(95%CI): 2.85(1.46, 5.57) and 2.90(1.48, 5.68), respectively]. The presence of one of these risk factors increased the 30-day mortality rate by 6-fold [HR = 6.24, 95%CI: (3.18, 12.22)] and the presence of two risk factors by nearly 10-fold [HR = 9.98, 95%CI: (4.23, 23.56)] compared with the patients with no risk factors.
Severe derangement of lipoproteins is common in children with HLH, and decreased TC is an independent risk factor for early death. Hypocholesterolemia should be included as a biomarker during the diagnosis and management of HLH patients.
噬血细胞性淋巴组织细胞增生症(HLH)是一种进展迅速且可能危及生命的疾病。识别风险因素并及时调整既定治疗方案对于降低HLH患者的早期死亡率至关重要。据报道,低胆固醇血症与多种危重症的不良预后相关。然而,HLH患者的血清胆固醇很少被研究,其预后价值尚不清楚。
我们在国家儿童健康与疾病临床医学研究中心(重庆)进行了一项回顾性队列研究,纳入2008年1月至2020年12月期间根据HLH - 2004方案诊断并接受免疫化疗的儿科HLH患者(包括基因确诊的pHLH和未基因确诊的pHLH)。根据电子病历回顾HLH初诊时患者的血脂水平,包括甘油三酯(TG)、总胆固醇(TC)、高密度脂蛋白胆固醇(HDL - C)、低密度脂蛋白胆固醇(LDL - C)。采用Cox和逻辑回归模型评估血脂指标对早期死亡(诊断后30天内)的影响。
共纳入353例患者,诊断时的中位年龄为45个月。观察到的30天死亡率为19.05%(64/336,17例失访),Kaplan - Meier估计的3年生存率为61.67%(95%CI,56.27% - 67.59%)。173例(49.0%,173/353)患者进行了HLH相关基因的DNA靶向测序(并非所有疑似pHLH患者都接受了基因检测),29例被诊断为基因确诊的pHLH。349例患者进行了血脂检测:91.98%(321/349)的TG≥1.80 mmol/L,62.75%(219/349)的TG≥3.00 mmol/L,92.84%(324/349)的HDL - C≤1.04 mmol/L,58.74%(205/349)的LDL - C≤1.30 mmol/L,24.64%(86/349)的TC≤3.11 mmol/L。TC≤3.11 mmol/L和BUN≥7.14 mmol/L是30天死亡率的独立危险因素[HR(95%CI):分别为2.85(1.46, 5.57)和2.90(1.48, 5.68)]。与无危险因素的患者相比,存在其中一个危险因素使30天死亡率增加6倍[HR = 6.24,95%CI:(3.18, 12.22)],存在两个危险因素使死亡率增加近10倍[HR = 9.98,95%CI:(4.23, 23.56)]。
HLH患儿中脂蛋白严重紊乱很常见,TC降低是早期死亡的独立危险因素。低胆固醇血症应作为HLH患者诊断和管理过程中的一个生物标志物。