Hall Glen H, Atkin Stephen L, Turnbull Lindsay W
Department of Radiology, Centre for Magnetic Resonance Investigations, Department of Diabetes and Endocrinology, Michael White Diabetes Centre, Hull Royal Infirmary, University of Hull, Hull, U.K.
J Reprod Med. 2002 Feb;47(2):107-14.
To assess the ability of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to measure functional vascular pharmacokinetic parameters of normal human ovaries in vivo using an open linear two-compartment pharmacokinetic model.
Twenty-one women with no ovarian disease underwent DCE-MRI. Sequential images were acquired during injection of a contrast bolus. Ovarian volumes were calculated and pharmacokinetic data analyzed using a pharmacokinetic model. Ovarian tissue was compared with skeletal muscle to demonstrate the pharmacokinetic parameters.
Normal ovarian tissue was found to enhance rapidly and dramatically. When compared with skeletal muscle as a control, ovarian tissue was seen to demonstrate a significantly higher maximum enhancement factor and amplitude of the upslope, although there was no significant difference in the exchange rate. Sample size precluded conclusions about differences due to menstrual cycle or menopausal status.
The results reflect the vascular physiology of the normal ovary. Definition of the pharmacokinetic properties of normal ovaries will allow DCE-MRI to be applied prospectively to conduct noninvasive, in vivo studies of ovarian angiogenic function, including response to drugs, contraceptive research, assessment of polycystic ovary syndrome, ovarian hyperstimulation syndrome, diagnosis of malignancy and prediction of response to antiangiogenic chemotherapy.
使用开放线性双室药代动力学模型,评估动态对比增强磁共振成像(DCE-MRI)在体内测量正常人类卵巢功能血管药代动力学参数的能力。
21名无卵巢疾病的女性接受了DCE-MRI检查。在注射对比剂团注期间采集序列图像。计算卵巢体积,并使用药代动力学模型分析药代动力学数据。将卵巢组织与骨骼肌进行比较以展示药代动力学参数。
发现正常卵巢组织增强迅速且显著。与作为对照的骨骼肌相比,卵巢组织显示出明显更高的最大增强因子和上升斜率幅度,尽管交换率没有显著差异。样本量排除了关于月经周期或绝经状态差异的结论。
结果反映了正常卵巢的血管生理学。正常卵巢药代动力学特性的定义将使DCE-MRI能够前瞻性地应用于进行卵巢血管生成功能的非侵入性体内研究,包括对药物的反应、避孕研究、多囊卵巢综合征评估、卵巢过度刺激综合征、恶性肿瘤诊断以及抗血管生成化疗反应预测。