Published online before print February 20, 2006, doi: 10.1161/01.HYP.0000208994.69007.3e
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(Hypertension. 2006;47:e16.)
© 2006 American Heart Association, Inc.
Letters to the Editor |
Uterine Artery Doppler and Changes in Endothelial Function Before Clinical Disease in Preeclamptic Women
Department of Obstetrics and Gynecology, Assistance Publique-Hôpitaux de Paris, France
An extract of the first 100% of the full text is provided, because this article has no abstract. |
To the Editor:
Khan et al1 screened women for increased risk of preeclampsia using uterine artery Doppler waveforms at 18 to 20 weeks gestation. However, at this gestational age a high proportion of the abnormal waveforms may still normalize. Bower et al showed that 16% of 2058 unselected women had abnormal flow velocity waveforms at 18 to 22 weeks gestation versus 5.1% at 24 weeks gestation,2 and the persistent-notching is strongly predictive of early onset preeclampsia.3 Although Khan et al did not perform this 2-stage Doppler screening, they stated that there were no significant differences in vascular responses to acetylcholine and sodium nitroprusside between women with normal and abnormal Doppler waveforms at any time point. Conversely, they observed that microvascular responses for acetylcholine and for sodium nitroprusside were augmented in women in whom preeclampsia subsequently developed compared with those in normotensive women. Actually, they compared preeclamptic women of whom 73% (11 of 15) had preterm preeclampsia with 18 to 20 weeks gestation notching and an unknown but probably high proportion of persistently abnormal Doppler waveforms3 to normal women with an unknown but probably low proportion of persistently abnormal Doppler waveforms.
The investigation of the potential sensitivity of the microcirculation to NO in these preeclamptic notched patients (which cannot really be extrapolated from this work) would have been of much interest because several studies reported the improvement of abnormal uterine artery impedance with NO donors in preeclamptic women and support the hypothesis of NO deficiency in these women.4,5
1. Khan F, Belch JJ, MacLeod M, Mires G. Changes in endothelial function precede the clinical disease in women in whom preeclampsia develops. Hypertension. 2005; 46: 1123–1128.
2. Bower S, Bewley S, Campbell S. Improved prediction of preeclampsia by two-stage screening of uterine arteries using the early diastolic notch and color Doppler imaging. Obstet Gynecol. 1993; 82: 78–83.[Medline] [Order article via Infotrieve]
3. Aardema MW, De Wolf BT, Saro MC, Oosterhof H, Fidler V, Aarnoudse JG. Quantification of the diastolic notch in Doppler ultrasound screening of uterine arteries. Ultrasound Obstet Gynecol. 2000; 16: 630–634.[Medline] [Order article via Infotrieve]
4. Thaler I, Amit A, Kamil D, Itskovitz-Eldor J. The effect of isosorbide dinitrate on placental blood flow and maternal blood pressure in women with pregnancy induced hypertension. Am J Hypertens. 1999; 12: 341–347.[Medline] [Order article via Infotrieve]
5. Nakatsuka M, Takata M, Tada K, Asagiri K, Habara T, Noguchi S, Kudo T. A long-term transdermal nitric oxide donor improves uteroplacental circulation in women with preeclampsia. J Ultrasound Med. 2002; 21: 831–836.
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  B. D. LaMarca, J. Gilbert, and J. P. Granger Recent Progress Toward the Understanding of the Pathophysiology of Hypertension During Preeclampsia Hypertension, April 1, 2008; 51(4): 982 - 988. [Full Text] [PDF]
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