Goates J J, Morton K A, Whooten W W, Greenberg H E, Datz F L, Handy J E, Scuderi A J, Haakenstad A O, Lynch R E
Nuclear Medicine Service, VA Medical Center, Salt Lake City, Utah.
J Nucl Med. 1990 Apr;31(4):424-9.
True glomerular filtration rate (GFR) was measured in normal volunteers and in patients with normal and impaired renal function by the iothalamate clearance (IC) method of Sigman. Within 24 hr, GFR was also determined by two other methods: technetium-99m- (99mTc) DTPA scintigraphic analysis (SA) utilizing a modification of the Gates computer program, and by measuring disappearance of 99mTc-DTPA from whole plasma (WPC) and from protein-free ultrafiltered plasma (PFPC). Determinations of GFR by IC and by PFPC methods were virtually identical (mean absolute error 5.36 ml/min, r = 0.99, p greater than 0.05). GFRs measured in protein-free, ultrafiltered plasma differed significantly from those obtained from whole plasma only in sicker patients and in those taking multiple medications (in whom alterations in protein-binding of DTPA may be seen). The SA method correlated less well with the iodine-125-(125I) IC method than did either the protein-free or whole-plasma clearance methods (mean absolute error 32.36 ml/min, r = 0.74, p less than 0.05). However, the SA method provided useful information with respect to differential (split) renal function.
通过西格曼的碘肽酸盐清除率(IC)方法,对正常志愿者以及肾功能正常和受损的患者测量了真实肾小球滤过率(GFR)。在24小时内,还通过其他两种方法测定了GFR:利用盖茨计算机程序的改良版进行锝-99m(99mTc)二乙三胺五乙酸(DTPA)闪烁扫描分析(SA),以及测量99mTc-DTPA在全血浆(WPC)和无蛋白超滤血浆(PFPC)中的消失情况。通过IC方法和PFPC方法测定的GFR几乎相同(平均绝对误差为5.36 ml/分钟,r = 0.99,p大于0.05)。仅在病情较重的患者以及服用多种药物的患者(可能出现DTPA蛋白结合改变的患者)中,无蛋白超滤血浆中测量的GFR与全血浆中获得的GFR有显著差异。SA方法与碘-125(125I)IC方法的相关性不如无蛋白或全血浆清除率方法(平均绝对误差为32.36 ml/分钟,r = 0.74,p小于0.05)。然而,SA方法提供了关于分肾功能的有用信息。