Xu Chenglin, Wen Song, Gong Min, Dong Meiyuan, Yuan Yue, Li Yanyan, Zhou Mingyue, Zhou Ligang
Department of Endocrinology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, 201399, People's Republic of China.
Fudan Zhangjiang Institute, Fudan University, Shanghai, 201203, People's Republic of China.
Diabetes Metab Syndr Obes. 2024 Jul 1;17:2639-2653. doi: 10.2147/DMSO.S465311. eCollection 2024.
To investigate the implications of elevated myoglobin (MYO) in acute diabetic conditions of diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic state (HHS).
This study integrates in-patient data from Shanghai Pudong Hospital from 2019 to 2023. Laboratory data were compared between stable T2D patients (without acute diabetic complications), DKA, and HHS patients. The multilinear regression explored variables relevant to the elevated MYO in DKA and HHS. The dynamics of MYO, the survival rate, and associated risk factors in HHS were determined.
Except for triglyceride, procalcitonin, low-density lipoprotein, islet cell autoimmune antibodies, N-terminal Pro-brain natriuretic peptide (NT-ProBNP), and brain natriuretic peptide (BNP), there were significant differences in age, gender distribution, duration of diabetes, type of diabetes, and other referred laboratory data (p<0.05). The age, gender, creatine kinase (CK), estimated glomerular filtration rate (eGFR), and free triiodothyronine (FT3) in DKA, whereas osmolar, uric acid (UA), and cardiac troponin I (cTNI) in the HHS, were significant determinants of elevated MYO, respectively (p<0.05). The dynamic of MYO in HHS was in line with the survival trend, where the percentage of death was 29.73%, and aging with higher procalcitonin levels was a key risk factor. Besides, the cumulative survival rates between patients with or without bone fracture or muscle injury were substantially different.
This real-world study demonstrated DKA and HHS potentially have unique causes for increased MYO. By utilizing the appropriate regression parameters, we could forecast the progression of increased MYO in groups of DKA and HHS, while based on risk factors of aging, severity of infection, and different MYO sources, we could predict the prognosis of HHS.
探讨肌红蛋白(MYO)升高在糖尿病酮症酸中毒(DKA)和高渗高血糖状态(HHS)等急性糖尿病病情中的意义。
本研究整合了上海浦东医院2019年至2023年的住院患者数据。对稳定的2型糖尿病患者(无急性糖尿病并发症)、DKA患者和HHS患者的实验室数据进行了比较。多线性回归分析了与DKA和HHS中MYO升高相关的变量。确定了HHS中MYO的动态变化、生存率及相关危险因素。
除甘油三酯、降钙素原、低密度脂蛋白、胰岛细胞自身抗体、N末端脑钠肽前体(NT-ProBNP)和脑钠肽(BNP)外,年龄、性别分布、糖尿病病程、糖尿病类型及其他相关实验室数据存在显著差异(p<0.05)。DKA中的年龄、性别、肌酸激酶(CK)、估算肾小球滤过率(eGFR)和游离三碘甲状腺原氨酸(FT3),以及HHS中的渗透压、尿酸(UA)和心肌肌钙蛋白I(cTNI)分别是MYO升高的显著决定因素(p<0.05)。HHS中MYO的动态变化与生存趋势一致,死亡率为29.73%,年龄增长和降钙素原水平升高是关键危险因素。此外,有或无骨折或肌肉损伤患者的累积生存率存在显著差异。
这项真实世界研究表明,DKA和HHS中MYO升高可能有独特原因。通过使用适当的回归参数,我们可以预测DKA和HHS组中MYO升高的进展,而基于年龄、感染严重程度和不同MYO来源的危险因素,我们可以预测HHS的预后。