Urinary protein patterns and preeclampsia.

F J Kaltenbach, W H Boesken, C Wilhelm, J Ziupa, M N Toussaint, L Quaas
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引用次数: 10

Abstract

A retrospective study of urinary protein patterns, as determined by SDS-PAA-disc-electrophoresis was performed in 107 patients in third trimester of pregnancy because of preeclampsia. The aim was to determine whether the protein patterns allow a differentiation between nephropathies associated with genuine toxaemia of pregnancy and those in which toxaemia was superimposed on preexisting renal glomerular or tubular disease. The magnitude and type of proteinuria was related to the mean arterial pressure (MAP). 47% of all patients showed a mixed protein pattern independent of the MAP-severity. This form of proteinuria is probably associated with a genuine toxaemia of pregnancy. It was not possible to determine if pure glomerulopathies whose frequency rose with MAP, had already been present before pregnancy. In a third of the 22 patients followed-up post-partum pathological protein patterns or increased protein excretion was detected. This implies that 35% of the nephropathies were present before pregnancy. However, differentiation between preexisting and toxaemia associated nephropathy was not always possible. SDS-PAA-analysis of urinary protein should be carried out in earlier stages of pregnancy in cases of increasing MAP and proteinuria.

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尿蛋白模式和先兆子痫。
对107例因先兆子痫导致的妊娠晚期患者进行了sds - paa盘电泳测定尿蛋白模式的回顾性研究。目的是确定蛋白质模式是否允许区分与妊娠真实毒血症相关的肾病和那些毒血症叠加于先前存在的肾小球或肾小管疾病的肾病。蛋白尿的大小和类型与平均动脉压(MAP)有关。47%的患者表现出与map严重程度无关的混合蛋白模式。这种形式的蛋白尿可能与真正的妊娠毒血症有关。单纯肾小球病变(其频率随MAP升高)在妊娠前是否已经存在是不可能确定的。在22名患者中,有三分之一的患者在产后随访中检测到病理蛋白模式或蛋白质排泄增加。这意味着35%的肾病在怀孕前就存在了。然而,区分已存在的和毒血症相关性肾病并不总是可能的。在妊娠早期MAP和蛋白尿增加的情况下,应进行sds - paa尿蛋白分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Pre-eclampsia in a second pregnancy. A clinical follow-up study of 260 women with hypertension in pregnancy. Beta blocker therapy in 125 cases of hypertension during pregnancy. Disposition of the adrenergic blocker metoprolol in the late pregnant women, the amniotic fluid, the cord blood and the neonate. Maternal-fetal immunity: presence of specific cellular hyporesponsiveness and humoral suppressor activity in normal pregnancy and their absence in preeclampsia.
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