Liang Xiao, Yang Gaohui, Shi Lingling, Liu Lianjin, Wei Zhenbin, Huang Yumei, Bai Jing, Liang Yi, Pan Lingyuan, Gan Zhaoping, Lin Yu, Yao Yibin, Tang Ying, Huang Huicheng, Zhou Xuemei, Lai Yongrong, Liu Rongrong
Department of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Heliyon. 2024 Sep 19;10(19):e38069. doi: 10.1016/j.heliyon.2024.e38069. eCollection 2024 Oct 15.
Research into the pulmonary function of patients with transfusion-dependent thalassemia (TDT) is limited, with existing studies presenting conflicting results. We carried out a retrospective study involving 140 patients with TDT. The mean patient age was 8.7 ± 3.2 years, with a median serum ferritin (SF) level of 3791.4 ng/ml (IQR: 2424.1-5733.3 ng/ml). Pulmonary function abnormalities were detected in 46.43 % (65 out of 140) of patients, primarily manifesting as diffusion dysfunction (26.43 %), followed by ventilatory dysfunction (5.0 %), and mixed pulmonary dysfunction (15.0 %). A serum ferritin level above 2500 ng/ml significantly correlated with the occurrence of these abnormalities(OR = 3.187, 95%CI:1.312-7.741, P = 0.010), while higher hemoglobin concentrations demonstrated a protective effect (OR = 0.966, 95%CI: 0.943-0.989, P = 0.004). Our study highlights diffusion dysfunction as the most prevalent type of pulmonary function abnormalities in TDT patients. Furthermore, it establishes a correlation between elevated serum ferritin levels and pulmonary dysfunction.
对依赖输血的地中海贫血(TDT)患者的肺功能研究有限,现有研究结果相互矛盾。我们进行了一项回顾性研究,涉及140例TDT患者。患者平均年龄为8.7±3.2岁,血清铁蛋白(SF)水平中位数为3791.4 ng/ml(四分位间距:2424.1 - 5733.3 ng/ml)。46.43%(140例中的65例)的患者检测到肺功能异常,主要表现为弥散功能障碍(26.43%),其次是通气功能障碍(5.0%)和混合性肺功能障碍(15.0%)。血清铁蛋白水平高于2500 ng/ml与这些异常的发生显著相关(OR = 3.187,95%CI:1.312 - 7.741,P = 0.010),而较高的血红蛋白浓度显示出保护作用(OR = 0.966,95%CI:0.943 - 0.989,P = 0.004)。我们的研究强调弥散功能障碍是TDT患者中最常见的肺功能异常类型。此外,它还确立了血清铁蛋白水平升高与肺功能障碍之间的相关性。