Dokuz Eylül University, Izmir, Turkey.
Division of Metabolism, Endocrine & Diabetes and Brehm Center for Diabetes Research, Department of Internal Medicine, Michigan Medicine, University of Michigan, Ann Arbor, Michigan.
J Clin Endocrinol Metab. 2019 Nov 1;104(11):5120-5135. doi: 10.1210/jc.2018-02730.
Limited natural history data are available in patients with non-HIV-related lipodystrophy syndromes who never received disease-specific therapies, making interpretation of benefits of therapies in lipodystrophy syndromes challenging.
We assessed the natural history of non-HIV-related generalized lipodystrophy (GL) and partial lipodystrophy (PL) in patients who have never received leptin or other lipodystrophy-specific therapies.
DESIGN/SETTING/PATIENTS: We conducted an international chart review of 230 patients with confirmed GL or PL at five treatment centers who never received leptin or other lipodystrophy-specific therapies. Patients were observed from birth to loss to follow-up, death, or date of chart abstraction.
Lifetime prevalence of diabetes/insulin resistance and select organ abnormalities, time to diabetes/insulin resistance, first organ abnormality, disease progression, and mortality were described.
Diabetes/insulin resistance was identified in 58.3% of patients. Liver abnormalities were the most common organ abnormality (71.7%), followed by kidney (40.4%), heart (30.4%), and pancreatitis (13.0%). Kaplan-Meier estimates of mean (SE) time to first organ abnormality were 7.7 years (0.9) in GL and 16.1 years (1.5) in PL (P < 0.001). Mean time to diabetes/insulin resistance was 12.7 years (1.2) in GL and 19.1 years (1.7) in PL (P = 0.131). Mean time to disease progression was 7.6 years (0.8) and comparable between GL and PL subgroups (P = 0.393). Mean time to death was 51.2 years (3.5) in GL and 66.6 years (1.0) in PL (P < 0.001).
This large-scale study provides comprehensive, long-term data across multiple countries on the natural history of non-HIV-related lipodystrophy.
在从未接受过疾病特异性治疗的非 HIV 相关脂肪代谢障碍综合征患者中,可用的自然病史数据有限,这使得脂肪代谢障碍综合征中治疗益处的解释具有挑战性。
我们评估了从未接受过瘦素或其他脂肪代谢障碍特异性治疗的非 HIV 相关全身性脂肪营养不良 (GL) 和部分脂肪营养不良 (PL) 患者的自然病史。
设计/设置/患者:我们对五个治疗中心的 230 名经证实的 GL 或 PL 患者进行了国际图表回顾,这些患者从未接受过瘦素或其他脂肪代谢障碍特异性治疗。患者从出生开始接受观察,直至随访丢失、死亡或图表摘录日期。
描述了终生糖尿病/胰岛素抵抗和选定器官异常的患病率、糖尿病/胰岛素抵抗的发生时间、首次器官异常、疾病进展和死亡率。
这项大规模研究提供了关于非 HIV 相关脂肪代谢障碍的多国家、长期的自然病史综合数据。