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DOI: 10.1055/a-2784-5163
Impact of Diurnal Variation on Umbilical Artery Doppler Measurements in Pregnancies Complicated by Hypertensive Disorders
Authors
Abstract
Objective
The study aims to determine whether the time of day influences these parameters compared to normotensive pregnancies.
Materials and Methods
This prospective, single-center study included 60 pregnant women diagnosed with hypertensive disorders (gestational hypertension, chronic hypertension, or preeclampsia) and 60 normotensive controls, all between 30 and 37 weeks of gestation. Umbilical artery Doppler measurements were performed twice daily, between 08:00–10:00 and 20:00–22:00, by the same experienced operator. Measurements were taken at both the fetal and placental ends of the umbilical artery, recording systolic/diastolic ratios, pulsatility index, and resistance index values.
Results
In Doppler measurements, the morning and evening evaluations revealed that S/D, PI, and RI values near the fetus and placenta were significantly higher in the study group compared to the control group. Notably, in the preeclampsia subgroup, the morning S/D values (3.3±1.1 vs. 2.3±0.5, p<0.001) were found to reach the highest levels. Regarding neonatal outcomes, the study group demonstrated significantly higher rates of cesarean delivery (71.7% vs. 33.3%, p<0.001) and neonatal intensive care unit admission (36.7% vs. 6.7%, p<0.001), while birth weight was significantly lower (2724.9±759.1 g vs. 3241.1±422.7 g, p<0.001).
Conclusion
This study demonstrates that hypertensive disorders during pregnancy have a significant adverse effect on umbilical artery Doppler measurements and neonatal outcomes. These findings underscore the importance of early diagnosis and meticulous monitoring.
Keywords
Hypertensive disorders - umbilical artery - doppler - preeclampsia - diurnal circadian rhythm - perinatal outcomesPublication History
Received: 10 July 2025
Accepted after revision: 08 January 2026
Article published online:
03 February 2026
© 2026. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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References
- 1 Wu P, Green M, Myers JE. Hypertensive disorders of pregnancy. BMJ 2023; 381: e071653
- 2 Mecacci F, Romani E, Clemenza S. et al. Early fetal growth restriction with or without hypertensive disorders: a clinical overview. Reprod Sci 2024; 31: 591-602
- 3 Roberge S, Bujold E, Nicolaides KH. Meta-analysis on the effect of aspirin use for prevention of preeclampsia on placental abruption and antepartum hemorrhage. Am J Obstet Gynecol 2018; 218: 483-489
- 4 Rocha AS, Andrade ARA, Moleiro ML. et al. Doppler ultrasound of the umbilical artery: clinical application. Rev Bras Ginecol Obstet 2022; 44: 519-531
- 5 Mahajan KS, Dewani D, Duragkar S. Umbilical artery Doppler Indices in hypertensive disorders of pregnancy: Impact on fetal outcomes. Cureus 2023; 15: e50876
- 6 Arakaki T, Hasegawa J, Takita H. et al. Can umbilical artery Doppler findings at 36 weeks' gestation predict maternal hypertension at later gestation?. J Matern Fetal Neonatal Med 2017; 30: 177-180
- 7 Lal H, Verma SK, Wang Y. et al. Circadian rhythms in cardiovascular metabolism. Circ Res 2024; 134: 635-658
- 8 Karabulut S, Oria L. The effects of circadian rhythm on reproductive functions. Zygote 2025; 33: 203-209
- 9 Méndez N, Corvalan F, Halabi D. et al. From gestational chronodisruption to noncommunicable diseases: Pathophysiological mechanisms of programming of adult diseases, and the potential therapeutic role of melatonin. J Pineal Res 2023; 75: e12908
- 10 Waddell BJ, Wharfe MD, Crew RC. et al. A rhythmic placenta? Circadian variation, clock genes and placental function. Placenta 2012; 33: 533-539
- 11 Mark PJ, Crew RC, Wharfe MD. et al. Rhythmic three-part harmony: The complex interaction of maternal, placental and fetal circadian systems. J Biol Rhythms 2017; 32: 534-549
- 12 Chuffa LGA, Lupi LA, Cucielo MS. et al. Melatonin promotes uterine and placental health: potential molecular mechanisms. Int J Mol Sci 2019; 21: 300
- 13 Staboulidou I, Wüstemann M, Schmidt P. et al. Influence of circadian rhythm on fetal and maternal Doppler parameters. Z Geburtshilfe Neonatol 2008; 212: 47-52
- 14 14 Avitan T, Sanders A, Brain U. et al. Variations from morning to afternoon of middle cerebral and umbilical artery blood flow, and fetal heart rate variability, and fetal characteristics in the normally developing fetus. J Clin Ultrasound 2018; 46: 235-240
- 15 Maulik D, Yarlagadda AP, Youngblood JP. et al. Components of variability of umbilical arterial Doppler velocimetry. Am J Obstet Gynecol 1989; 160: 1406-1412
- 16 Bhide A, Badade A, Khatal K. The effect of sampling site on the variability of umbilical artery PI. Eur J Obstet Gynecol Reprod Biol 2019; 235: 102-105
- 17 Rühle W, Gnirs J, Schmidt W. et al. Fetal heart rate and Doppler flow parameters in fetal blood vessels. Z Geburtshilfe Perinatol 1993; 197: 90-94
- 18 Yarlagadda P, Willoughby L, Maulik D. Effect of fetal heart rate on umbilical arterial Doppler indices. J Ultrasound Med 1989; 8: 215-218
- 19 Chiba Y, Utsu M, Kanzaki T. et al. Changes in venous flow and intratracheal flow in fetal breathing movements. Ultrasound Med Biol 1985; 11: 43-49
- 20 Mulders LG, Muijsers GJ, Jongsma HW. et al. The umbilical artery blood flow velocity waveform in relation to fetal breathing movements, fetal heart rate and fetal behavioural states in normal pregnancy at 37 to 39 weeks. Early Hum Dev 1986; 14: 283-293
- 21 Tekin S, Öcal A. Diurnal variation of fetomaternal Doppler and fetal cardiac function parameters in the hospitalized pregnancies: A cross-sectional study. Istanb Med J 2024; 25: 116-120
