Diagnostic value of the myocardial performance index and doppler parameters in detecting fetal growth restriction in pregnancies complicated by hypertensive disorders
Original Article

Diagnostic value of the myocardial performance index and doppler parameters in detecting fetal growth restriction in pregnancies complicated by hypertensive disorders

Yao Peng1,2#, Wei Feng1#, Sitong Yue1#, Yang He2, Xue Liao2, Zixian Wei1, Ling Gan1,2, Jiaqi Zhang1,2 ORCID logo

1Hubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Department of Ultrasound, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, China; 2Department of Ultrasound Imaging, Postgraduate Union Training Base of Xiangyang No. 1 People’s Hospital, School of Medicine, Wuhan University of Science and Technology, Xiangyang, China

Contributions: (I) Conception and design: J Zhang, L Gan; (II) Administrative support: J Zhang, L Gan; (III) Provision of study materials or patients: Y Peng, W Feng; (IV) Collection and assembly of data: Y Peng, W Feng; (V) Data analysis and interpretation: S Yue, Y He, X Liao, Z Wei; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

#These authors contributed equally to this work.

Correspondence to: Dr. Ling Gan, MS; Dr. Jiaqi Zhang, MD. Department of Ultrasound Imaging, Postgraduate Union Training Base of Xiangyang No. 1 People’s Hospital, School of Medicine, Wuhan University of Science and Technology, No. 15 Jiefang Road, Xiangyang 441000, China; Hubei Provincial Clinical Research Center for Accurate Fetus Malformation Diagnosis, Department of Ultrasound, Xiangyang No. 1 People’s Hospital, Hubei University of Medicine, Xiangyang, China. Email: xyyycsgl@163.com; 347235272@qq.com.

Background: Hypertensive disorders in pregnancy (HDP) are conditions that may affect fetal growth and development. This study aimed to assess the diagnostic value of the myocardial performance index (MPI) and Doppler parameters in identifying fetal growth restriction (FGR) in HDP. Further, this study also sought to analyze the correlation between fetal echocardiographic parameters and pregnancy outcomes.

Methods: A total of 202 pregnant women at Xiangyang No. 1 People’s Hospital were recruited for this prospective study and allocated to three groups: the healthy control group (n=95), HDP without FGR group (n=75), and HDP with FGR group (n=32). Fetal cardiac assessments included measurements of the MPI, umbilical artery pulsatility index (UA-PI), and middle cerebral artery pulsatility index (MCA-PI), with additional fetal and maternal clinical data collected. Statistical analyses were performed to compare these parameters among groups, and correlation analyses were performed to examine the relationships between birth weight and Doppler, clinical, and cardiac parameters.

Results: The HDP with FGR group exhibited a significantly higher MPI (0.48±0.08 vs. 0.42±0.05, P<0.001) and UA-PI (1.23±0.20 vs. 0.89±0.14, P<0.001) compared to the control group. Significant negative correlations were observed between birth weight and the MPI (r=–0.405, P=0.036), as well as between birth weight and the UA-PI (r=–0.317, P=0.039). In the receiver operating characteristic (ROC) curve analysis distinguishing HDP with FGR from HDP with normal fetal growth, estimated fetal weight (EFW) and the UA-PI demonstrated the highest discriminative power [area under the curve (AUC) =0.86 for both], followed by the MPI [AUC =0.78, 95% confidence interval (CI): 62.0–94.4%].

Conclusions: HDP with FGR was found to be associated with significant fetal cardiac dysfunction and increased placental resistance. The MPI and UA-PI could serve as effective quantitative markers for detecting FGR in hypertensive pregnancies. The significant correlation between these parameters and birth weight supports their clinical utility for early detection and targeted monitoring in high-risk pregnancies.

Keywords: Fetal growth restriction (FGR); hypertensive disorders in pregnancy (HDP); myocardial performance index (MPI); Doppler parameters


Submitted Sep 24, 2025. Accepted for publication Feb 21, 2026. Published online Apr 09, 2026.

doi: 10.21037/qims-2025-2056


Introduction

Hypertensive disorders in pregnancy (HDP), such as gestational hypertension and preeclampsia, are among the most common complications affecting maternal and fetal health, occurring in approximately 5–10% of pregnancies worldwide (1). These conditions are associated with significant maternal and perinatal morbidity and mortality, primarily due to their adverse effects on placental function, leading to impaired fetal growth (2-4). One of the most concerning outcomes of hypertensive disorders is fetal growth restriction (FGR), a condition where the fetus fails to achieve its expected growth potential in utero (5,6). FGR is closely linked to perinatal complications, including preterm birth, stillbirth, and long-term neurodevelopmental and cardiovascular consequences for the offspring (7,8).

Hypertensive disorders disrupt placental blood flow, reducing oxygen and nutrient delivery to the fetus, which can impair fetal development and compromise organ function, including the heart (9,10). Previous research has demonstrated that fetuses with FGR often exhibit cardiac remodeling and dysfunction, with altered ventricular geometry and impaired systolic and diastolic performance (11,12). These changes may increase the risk of perinatal morbidity and even influence cardiovascular health later in life (13,14). However, there is still much to learn about the early detection of fetal cardiac dysfunction in pregnancies complicated by hypertensive disorders.

In recent years, fetal echocardiography has become a critical tool for evaluating fetal cardiac function, allowing clinicians to assess systolic and diastolic performance non-invasively. The myocardial performance index (MPI), also known as the Tei index, is an echocardiographic parameter that provides a comprehensive assessment of both systolic and diastolic function by measuring the ratio of isovolumetric contraction and relaxation times to the ejection time (ET) (15,16). The MPI is widely used due to its simplicity, reproducibility, and ability to detect subtle changes in cardiac function, even in the absence of overt structural abnormalities (17,18). Studies suggest that the MPI may be a valuable marker for identifying fetal cardiac dysfunction in pregnancies affected by FGR (19,20).

Additionally, studies report that other fetal blood flow spectral indices, including the umbilical artery pulsatility index (UA-PI), middle cerebral artery pulsatility index (MCA-PI), and ductus venosus pulsatility index (DV-PI), are valuable for assessing placental blood flow and fetal oxygenation status. The UA-PI reflects changes in placental vascular resistance, typically increasing in cases of FGR. The MCA-PI assesses cerebral blood flow, with a decrease often indicating “brain-sparing” due to fetal hypoxia (21). The DV-PI provides insights into fetal right heart function and venous return, with abnormal DV-PI suggesting potential risks of chronic hypoxia or heart failure (22). Therefore, the combined use of MPI with these spectral Doppler indices allows clinicians to more comprehensively assess fetal cardiac function and placental hemodynamics, offering a basis for timely intervention.

In summary, this study aimed to evaluate the diagnostic value of the MPI, in combination with the early (E) to late (A) diastolic filling (E/A) ratios of the mitral and tricuspid valves, and Doppler parameters of the umbilical artery, middle cerebral artery, and ductus venosus, in detecting FGR in pregnancies complicated by hypertensive disorders. By exploring the relationship between maternal hypertension, fetal cardiac function, and growth outcomes, we aimed to enhance early detection and improve management strategies for at-risk pregnancies. We present this article in accordance with the STROBE reporting checklist (available at https://qims.amegroups.com/article/view/10.21037/qims-2025-2056/rc).


Methods

Study population

A total of 284 pregnant women were recruited from the Department of Ultrasound Imaging at the Postgraduate Union Training Base of Xiangyang No. 1 People’s Hospital between April 2023 and October 2024. After applying the exclusion criteria, 202 participants were included in the study. Of the 202 participants, 95 were assigned to the control group, 75 to the HDP without FGR group, and 32 to the HDP with FGR group. Data collection included fetal biological indicators, Doppler blood flow indices, and clinical data, along with a comprehensive evaluation of fetal cardiac function. Statistical analyses were performed accordingly (Figure 1).

Figure 1 Study recruitment flowchart. FGR, fetal growth restriction; HDP, hypertensive disorders of pregnancy.

HDP was diagnosed according to the International Society for the Study of Hypertension in Pregnancy (ISSHP) (23) criteria for pregnancies with elevated blood pressure, defined as a systolic blood pressure ≥140 mmHg and/or a diastolic blood pressure ≥90 mmHg. FGR was diagnosed using the following criteria: an estimated fetal weight (EFW) below the 3rd percentile, or an EFW below the 10th percentile with accompanying Doppler evidence of placental dysfunction. This Doppler evidence included an UA-PI exceeding the 95th percentile, the absence of umbilical artery end-diastolic flow (UAEDF), reverse UAEDF, or a cerebroplacental ratio (CPR) below the 5th percentile (Figure 2). The exclusion criteria included chronic systemic diseases, multiple gestations, chronic drug use, fetal congenital and chromosomal abnormalities, and coexisting pregnancy complications such as gestational diabetes mellitus, preeclampsia, chorioamnionitis, and premature rupture of membranes, and/or refusal to participate in the study.

Figure 2 Doppler assessment of umbilical artery blood flow. The figure shows Doppler measurements of the umbilical artery. The prefix Umb- denotes parameters pertaining to the umbilical artery. Key parameters include: Umb-PS, Umb-ED, Umb-S/D, Umb-PI, Umb-RI, Umb-MD, Umb-TAMax, Umb-HR, Umb-VTI. ED, end-diastolic velocity; HR, fetal heart rate; MD, minimum diastolic velocity; PI, pulsatility index; PS, peak systolic velocity; RI, resistance index; S/D, systolic/diastolic ratio; TAMax, time-averaged maximum velocity; VTI, velocity-time integral.

All demographic data were collected from medical records. Maternal characteristics, including maternal age (MA) at recruitment, gestational age (GA) at recruitment, and body mass index (BMI), were documented. Obstetric characteristics, such as EFW and GA at delivery, were recorded. The neonatal characteristics included the neonatal weight percentile and birth weight.

GA was calculated from the last menstrual period and verified with first-trimester ultrasound measurements. Ultrasound evaluations were conducted using VOLUSON E10 ultrasound machines with the RM6C or C5-1 transducer (GE Healthcare, Chicago, IL, USA) by a single investigator with 10 years of obstetric experience. Following fetal anatomical assessment, fetal biometric parameters, EFW, and Doppler parameters were measured, including the DV-PI, UA-PI, MCA-PI, and MPI, with additional parameters recorded for the isovolumic relaxation time (IRT), isovolumic contraction time (ICT), ET, mitral valve early (E) to late (A) diastolic filling velocity ratio (MV-E/A ratio), tricuspid valve early (E) to late (A) diastolic filling velocity ratio (TV-E/A ratio), and CPR, calculated by dividing the MCA-PI by the UA-PI.

The study was conducted in accordance with the Declaration of Helsinki and its subsequent amendments. The study was approved by the Ethics Committee of Xiangyang No. 1 People’s Hospital, School of Medicine, Wuhan University of Science and Technology (No. 2021KYLX02). All participants provided written informed consent for fetal ultrasonography and were briefed on both the reliability and limitations of the procedure.

Measurement of fetal cardiac function

Initially, the apical four-chamber view of the fetal heart was obtained in a transverse section of the fetal thorax. From this view, the five-chamber perspective was achieved by cranially angulating the transducer. Once the aortic valve (AV) and mitral valve (MV) were clearly visible, a pulse Doppler sample gate was set to approximately 3–4 mm, ensuring it captured both the lateral wall of the ascending aorta and the internal leaflet of the MV. The angle of insonation was kept as low as possible, ideally aligned close to 0 degrees to the direction of blood flow, to minimize potential overestimation of the time intervals used for the MPI calculation. A high wall motion filter was calibrated to 300 Hz, and the Doppler gain was adjusted to minimize artifacts while clearly detecting valve clicks. Doppler waveforms representing the opening and closing of the MV and AV were recorded, with the Doppler sweep velocity set at 5 cm/s. The E wave (early ventricular filling) and A wave (active atrial filling) were identified, along with the flow pattern of the AV. The time cursor was placed at the onset of the clicks.

Three key intervals in the cardiac cycle were defined: the ICT, IRT, and ET. The ICT was measured from the beginning of MV closure to the end of AV opening, while the IRT was measured from MV opening to AV closure. The ET was defined as the time from AV opening to closure. The MPI was then calculated using the following formula: MPI = (ICT + IRT)/ET. To ensure reproducibility, each measurement was repeated three times, and the average value was used for analysis (Figure 3).

Figure 3 Measurement of MPI by Doppler ultrasound. The image shows the Doppler echocardiographic assessment of left ventricular function using the MPI. The MPI was calculated using time intervals derived from Doppler waveforms. LVOT-ICT: isovolumetric contraction time; LVOT-IRT: isovolumetric relaxation time; LVOT-Eject Time: left ventricular ejection time; LVOT-TEI (ICT, IRT): The Tei Index or MPI, calculated as the sum of ICT and IRT divided by the ejection time, yielding a value of 0.60. LVOT, left ventricular outflow tract; MPI, myocardial performance index.

Statistical analysis

The statistical analyses were conducted using SPSS version 26.0. Continuous variables were presented as the mean ± standard deviation (SD). The Kolmogorov-Smirnov test was used to evaluate the relevance of the data to normal distribution. The Mann-Whitney U-test was used to compare the statistical significance between two independent groups according to the distribution ranges. Spearman correlation tests were performed to assess the association of quantitative variables based on the distribution ratios. Receiver operating characteristic (ROC) curve analysis was used to determine the predictive accuracy for FGR and HDP. A P value less than 0.05 was considered statistically significant.


Results

Participant selection and final study cohort

In this study, 284 pregnant women initially volunteered to participate. Based on the exclusion criteria, 17 were excluded for chronic systemic diseases, 13 for multiple gestations, 15 for chronic drug use, 12 for fetal congenital or chromosomal abnormalities, 17 for coexisting pregnancy complications other than HDP, and eight for refusal to participate. Ultimately, 202 women were included in the final analysis; 95 were assigned to the control group, 75 to the HDP without FGR group, and 32 to the HDP with FGR group (Figure 1).

Comparison of maternal characteristics and neonatal outcomes

There were no statistically significant differences in BMI among the control, HDP without FGR, and HDP with FGR groups (P>0.05). However, significant differences were observed in MA at recruitment, GA at recruitment, EFW, GA at delivery, neonatal weight percentile, and birth weight across the groups (P<0.05). Specifically, MA and GA at recruitment were significantly higher in the HDP without FGR group than in the control and HDP with FGR groups (P<0.05). Additionally, EFW and GA at delivery were significantly lower in the HDP with FGR group than in both the control and HDP without FGR groups (P<0.05). The neonatal weight percentile and birth weight were also significantly reduced in the HDP with FGR group compared to both other groups (P<0.05) (Table 1).

Table 1

Maternal, obstetric, and neonatal characteristics

Variable Control (N=95) HDP without FGR (N=75) HDP with FGR (N=32) P value
Maternal characteristics
   MA at recruitment (years) 29.5±3.5 30.6±3.1a 28.7±3.8b 0.02
   GA at recruitment (weeks) 32.5±4.9 34.7±3.5a 31.4±4.2b <0.001
   BMI (kg/m2) 26.0±4.4 27.0±4.7 27.6±5.3 0.17
Obstetric characteristics
   EFW (grams) 2,263±605 2,279±683 1,347±512ab <0.001
   GA at delivery (weeks) 39.7±1.6 38.1±2.2a 33.1±3.6ab <0.001
Neonatal characteristics
   Neonatal weight percentile 48±19 53±28 5±3ab <0.001
   Birth weight (grams) 3,273±421 3,228±413 2,249±397ab <0.001

Data presented as the mean ± standard deviation. a, compared with the control group, P<0.05; b, compared with the HDP without FGR group, P<0.05. BMI, body mass index; EFW, estimated fetal weight; FGR, fetal growth restriction; GA, gestational age; HDP, hypertensive disorders of pregnancy; MA, maternal age.

Comparison of fetal cardiac function

Comparison of fetal cardiac function findings among the three groups (control, HDP without FGR, and HDP with FGR) demonstrated statistically significant differences in several parameters (P<0.05). Specifically, the MPI, MV-E/A ratio, TV-E/A ratio, UA-PI, MCA-PI, DV-PI, and CPR values varied significantly across the groups. In particular, the MPI, MV-E/A ratio, TV-E/A ratio, UA-PI, and DV-PI values were higher in the HDP groups compared to the control group (P<0.05), while the CPR values were lower. Further, the HDP with FGR group showed significantly lower CPR values but higher MPI, UA-PI, and DV-PI values compared to the HDP without FGR group (P<0.05) (Table 2).

Table 2

Comparison of fetal cardiac function findings of the patients

Variable Control (N=95) HDP without FGR (N=75) HDP with FGR (N=32) P value
IRT (ms) 40.8±6.1 41.5±6.7 42.8±7.3 0.320
ICT (ms) 32.2±6.0 33.7±6.5 35.3±5.6a 0.036*
ET (ms) 167.4±13.6 169.5±14.8 174.0±15.1 0.078
MPI (ms) 0.42±0.05 0.44±0.06 0.48±0.08ab 0.000*
MV-E/A ratio 0.66±0.13 0.72±0.16a 0.75±0.17a 0.003*
TV-E/A ratio 0.70±0.11 0.74±0.14 0.77±0.15a 0.015*
UA-PI 0.89±0.14 1.12±0.21a 1.23±0.20ab 0.000*
MCA-PI 1.96±0.68 1.80±0.72 1.63±0.84a 0.043*
DV-PI 0.50±0.21 0.56±0.24 0.62±0.30a 0.034*
CPR 2.19±0.41 1.73±0.36a 1.45±0.34ab 0.000*

Data presented as the mean ± standard deviation. *, P values are significant. a, compared with the control group, P<0.05; b, compared with the HDP without FGR group, P<0.05. CPR, cerebroplacental ratio; DV-PI, ductus venosus pulsatility index; ET, ejection time; FGR, fetal growth restriction; HDP, hypertensive disorders of pregnancy; ICT, isovolumic contraction period; IRT, isovolumic relaxation period; MCA-PI, middle cerebral artery pulsatility index; MPI, myocardial performance index; MV-E/A ratio, mitral valve early (E) to late (A) diastolic filling velocity ratio; TV-E/A ratio, tricuspid valve early (E) to late (A) diastolic filling velocity ratio; UA-PI, umbilical artery pulsatility index.

Correlation analysis of birth weight with gestational outcomes and fetal parameters

Spearman’s correlation tests revealed statistically significant positive correlations between birth weight and GA (r=0.634, P=0.012), as well as between birth weight and EFW (r=0.773, P=0.002). A significant negative correlation was observed between birth weight and MPI (r=–0.405, P=0.036), as well as birth weight and the UA-PI (r=–0.317, P=0.039). No statistically significant correlations were found between birth weight and other Doppler, clinical, and fetal cardiac parameters (Table 3).

Table 3

The correlations of birth weight with Doppler, clinical and cardiac parameters

Parameters Birth weight
r P value
GA of delivery 0.634* 0.012
BMI 0.213 0.169
UA-PI –0.317* 0.039
MCA-PI –0.176 0.492
DV-PI –0.023 0.893
EFW 0.773* 0.002
ICT –0.037 0.583
IRT –0.032 0.728
ET –0.147 0.521
MPI –0.405* 0.036
CPR –0.082 0.592

, Spearman’s correlation coefficient; *, significant values. A P value <0.05 indicated a statistically significant difference. BMI, body mass index; CPR, cerebroplacental ratio; DV-PI, ductus venosus pulsatility index; EFW, estimated fetal weight; ET, ejection time; GA, gestational age; ICT, isovolumetric contraction time; IRT, isovolumetric relaxation time; MCA-PI, middle cerebral artery pulsatility index; MPI, myocardial performance index; UA-PI, umbilical artery pulsatility index.

ROC curve analysis

The ROC curve analysis comparing normal pregnancies and those with HDP revealed that the UA-PI had the highest discriminative power with an ROC of 0.91 [95% confidence interval (CI): 87.0–92.1]. The ROC values for other indicators were as follows: ICT, 0.74 (95% CI: 55.2–84.4); EFW, 0.84 (95% CI: 69.5–94.8); CPR, 0.72 (95% CI: 54.3–90.6); MPI, 0.78 (95% CI: 66.5–89.7); and MV-E/A, 0.75 (95% CI: 57.0–92.3) (Figure 4).

Figure 4 ROC curve to predict HDP. CPR, cerebroplacental ratio; EFW, estimated fetal weight; HDP, hypertensive disorders of pregnancy; ICT, isovolumic contraction period; MPI, myocardial performance index; MV-E/A ratio, mitral valve early (E) to late (A) diastolic filling velocity ratio; ROC, receiver operating characteristic; UA-PI, umbilical artery pulsatility index.

The ROC curve analysis comparing pregnancies with HDP and normal fetal growth, as well as pregnancies with HDP and FGR showed an area under the curve [AUC] of 0.86 (95% CI: 77.0–97.9%) for EFW, 0.72 (95% CI: 50.4–93.4%) for the CPR, 0.86 (95% CI: 73.8–97.1%) for the UA-PI, and 0.78 (95% CI: 62.0–94.4%) for the MPI (Figure 5).

Figure 5 ROC curve to predict HDP with FGR. CPR, cerebroplacental ratio; EFW, estimated fetal weight; FGR, fetal growth restriction; HDP, hypertensive disorders of pregnancy; MPI, myocardial performance index; ROC, receiver operating characteristic; UA-PI, umbilical artery pulsatility index.

Discussion

The study results highlight the critical relationship between HDP and FGR, emphasizing the importance of early detection and monitoring of fetal cardiac function. The significant increase in MPI observed in the HDP with FGR group compared to the control group suggests that hypertensive disorders may lead to increased cardiac workload in fetuses, which is consistent with previous literature indicating that FGR fetuses often exhibit cardiac dysfunction and remodeling (24). This finding aligns with studies that have shown that fetal cardiac performance is adversely affected by placental insufficiency, a common consequence of hypertensive disorders (25,26). The negative correlation between the MPI and EFW further underscores the notion that as cardiac workload increases, fetal growth is compromised, potentially leading to adverse outcomes such as preterm birth and long-term cardiovascular issues in offspring.

Moreover, the study findings regarding the Doppler parameters, particularly the UA-PI, reinforce the utility of these measurements in clinical practice. The lower UA-PI in the HDP with FGR group compared to the control group indicates impaired placental perfusion, which is a hallmark of FGR. This is consistent with existing literature that demonstrates that Doppler ultrasound can effectively assess placental blood flow and predict adverse perinatal outcomes (27). The high AUC for the UA-PI in the ROC analysis further supports its role as a reliable diagnostic tool in identifying FGR in pregnancies complicated by hypertensive disorders. Such findings advocate for the integration of Doppler assessments into routine prenatal care for high-risk populations, enabling timely interventions that could improve fetal outcomes.

The study results also contribute to the growing body of evidence suggesting that the MPI can serve as a valuable marker for fetal cardiac dysfunction in the context of hypertensive disorders. The simplicity and reproducibility of MPI measurements make it an attractive option for clinicians seeking to monitor fetal well-being non-invasively. Previous studies have shown the efficacy of the MPI as an indicator of both systolic and diastolic function, reinforcing its potential as a prognostic tool in pregnancies complicated by FGR. The current findings suggest that the MPI, in conjunction with traditional Doppler parameters, could enhance the diagnostic accuracy for identifying fetuses at risk for growth restriction, thereby facilitating better management strategies (28,29).

Further, the correlation analysis, which revealed a significant positive relationship between EFW and both the MPI and Doppler parameters, emphasized the interconnectedness of fetal growth and cardiac function. This relationship suggests that monitoring these parameters could provide insights into the overall health of the fetus, enabling the proactive management of pregnancies at risk for complications. The implications of these findings extend beyond immediate clinical applications; they also highlight the need for further research into the mechanisms underlying fetal cardiac dysfunction in the context of hypertensive disorders. Understanding these mechanisms could pave the way for developing targeted interventions aimed at improving fetal outcomes in affected pregnancies (30-32).

In addition to the clinical implications, the study raises important considerations regarding the potential long-term consequences of FGR on cardiovascular health. Research has indicated that individuals who experienced FGR are at an increased risk for developing cardiovascular diseases later in life (33,34). This underscores the importance of not only identifying FGR during pregnancy but also implementing follow-up strategies to monitor the long-term health of these individuals. The findings of this study could inform future research aimed at elucidating the long-term effects of FGR on cardiovascular health and the potential benefits of early interventions.

The limitations of this study must be acknowledged. First, the sample size, while adequate for preliminary observations, imposes constraints. The cohort was unevenly distributed, with a notably larger control group compared to the high-risk HDP with FGR group. This significant disparity, though reflective of the lower prevalence of the severe comorbid condition in the clinical population, reduces the statistical power for inter-group comparisons and increases the risk of Type II errors, potentially masking subtle but real differences. It may also limit the robustness of multivariate adjustments and the feasibility of meaningful subgroup analyses within the HDP + FGR cohort. Second, regarding the methodological scope, our functional assessment was confined to conventional Doppler velocimetry and MPI derived from pulsed-wave Doppler. We did not employ more innovative and potentially sensitive modalities, such as speckle tracking echocardiography (STE). Recent evidence suggests that STE-derived strain and strain rate analysis can detect subclinical myocardial dysfunction, and provide incremental diagnostic and prognostic information over conventional parameters both in fetuses and in pregnancies complicated by hypertensive disorders (35,36). Consequently, while our findings highlight the utility of accessible conventional tools, they may not capture the full spectrum of early cardiac dysfunction. These limitations underscore the need to interpret our results as preliminary and hypothesis-generating. They strongly advocate for the future validation of these parameters in larger, prospective, and ideally balanced multicenter cohorts. Further, they point clearly to a promising research direction: integrating advanced quantitative techniques like STE with conventional biomarkers to develop more sensitive and comprehensive predictive models for FGR in high-risk pregnancies.


Conclusions

The study findings underscore the critical role of the MPI and Doppler parameters in the early detection of FGR in pregnancies complicated by hypertensive disorders. The significant alterations in fetal cardiac function associated with these conditions highlight the need for vigilant monitoring and proactive management strategies. By integrating these diagnostic tools into clinical practice, healthcare providers can improve outcomes for both mothers and their infants, ultimately contributing to a reduction in perinatal morbidity and mortality associated with HDP.


Acknowledgments

None.


Footnote

Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at https://qims.amegroups.com/article/view/10.21037/qims-2025-2056/rc

Data Sharing Statement: Available at https://qims.amegroups.com/article/view/10.21037/qims-2025-2056/dss

Funding: The study was supported by Hubei Provincial Natural Science Foundation (No. 2025AFB845) and Graduate Innovation and Entrepreneurship Fund of Wuhan University of Science and Technology (No. JCX2024044).

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://qims.amegroups.com/article/view/10.21037/qims-2025-2056/coif). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki and its subsequent amendments. The study was approved by the Ethics Committee of Xiangyang No. 1 People’s Hospital, School of Medicine, Wuhan University of Science and Technology (No. 2021KYLX02). All participants provided written informed consent for fetal ultrasonography and were briefed on both the reliability and limitations of the procedure.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Shang J, Dolikun N, Tao X, Zhang P, Woodward M, Hackett ML, Henry A. The effectiveness of postpartum interventions aimed at improving women’s mental health after medical complications of pregnancy: a systematic review and meta-analysis. BMC Pregnancy Childbirth 2022;22:809. [Crossref] [PubMed]
  2. ACOG Practice Bulletin No. 202: Gestational Hypertension and Preeclampsia. Obstet Gynecol 2019;133:1.
  3. Metoki H, Iwama N, Hamada H, Satoh M, Murakami T, Ishikuro M, Obara T. Hypertensive disorders of pregnancy: definition, management, and out-of-office blood pressure measurement. Hypertens Res 2022;45:1298-309. [Crossref] [PubMed]
  4. Wu P, Green M, Myers JE. Hypertensive disorders of pregnancy. BMJ 2023;381:e071653. [Crossref] [PubMed]
  5. Di Martino DD, Avagliano L, Ferrazzi E, Fusè F, Sterpi V, Parasiliti M, Stampalija T, Zullino S, Farina A, Bulfamante GP, Di Maso M, D'Ambrosi F. Hypertensive Disorders of Pregnancy and Fetal Growth Restriction: Clinical Characteristics and Placental Lesions and Possible Preventive Nutritional Targets. Nutrients 2022;14:3276. [Crossref] [PubMed]
  6. Lihme F, Basit S, Persson LG, Larsen MO, Lauridsen KH, Lykke JA, Andersen AS, Thorsen-Meyer A, Pihl K, Melbye M, Wohlfahrt J, Boyd HA. Third-Trimester Cardiovascular Function and Risk of Hypertensive Disorders of Pregnancy. J Am Heart Assoc 2024;13:e032673. [Crossref] [PubMed]
  7. Fetal Growth Restriction. ACOG Practice Bulletin, Number 227. Obstet Gynecol 2021;137:e16-28. [Crossref] [PubMed]
  8. Gordijn SJ, Beune IM, Thilaganathan B, Papageorghiou A, Baschat AA, Baker PN, Silver RM, Wynia K, Ganzevoort W. Consensus definition of fetal growth restriction: a Delphi procedure. Ultrasound Obstet Gynecol 2016;48:333-9. [Crossref] [PubMed]
  9. Gupta S, Petras L, Tufail MU, Rodriguez Salazar JD, Jim B. Hypertension in Pregnancy: What We Now Know. Curr Opin Nephrol Hypertens 2023;32:153-64. [Crossref] [PubMed]
  10. Lodge J, Flatley C, Kumar S. The fetal cerebroplacental ratio in pregnancies complicated by hypertensive disorders of pregnancy. Aust N Z J Obstet Gynaecol 2021;61:898-904. [Crossref] [PubMed]
  11. Melamed N, Baschat A, Yinon Y, Athanasiadis A, Mecacci F, Figueras F, et al. FIGO (international Federation of Gynecology and obstetrics) initiative on fetal growth: best practice advice for screening, diagnosis, and management of fetal growth restriction. Int J Gynaecol Obstet 2021;152:3-57. [Crossref] [PubMed]
  12. Nardozza LM, Caetano AC, Zamarian AC, Mazzola JB, Silva CP, Marçal VM, Lobo TF, Peixoto AB, Araujo Júnior E. Fetal growth restriction: current knowledge. Arch Gynecol Obstet 2017;295:1061-77. [Crossref] [PubMed]
  13. D'Agostin M, Di Sipio Morgia C, Vento G, Nobile S. Long-term implications of fetal growth restriction. World J Clin Cases 2023;11:2855-63. [Crossref] [PubMed]
  14. Mappa I, Maqina P, Bitsadze V, Khizroeva J, Makatsarya A, Arduini D, Rizzo G. Cardiac function in fetal growth restriction. Minerva Obstet Gynecol 2021;73:423-34. [PubMed]
  15. Oliveira M, Dias JP, Guedes-Martins L. Fetal Cardiac Function: Myocardial Performance Index. Curr Cardiol Rev 2022;18:e271221199505. [Crossref] [PubMed]
  16. Toumanidis ST. Myocardial performance index or Tei index: valuable in research but doubtful in clinical practice. Hellenic J Cardiol 2005;46:43-5. [PubMed]
  17. Bennett S, Cubukcu A, Wong CW, Griffith T, Oxley C, Barker D, Duckett S, Satchithananda D, Patwala A, Heatlie G, Kwok CS. The role of the Tei index in assessing for cardiotoxicity from anthracycline chemotherapy: a systematic review. Echo Res Pract 2021;8:R1-R11. [Crossref] [PubMed]
  18. Yuasa T, Miyazaki C, Oh JK, Espinosa RE, Bruce CJ. Effects of cardiac resynchronization therapy on the Doppler Tei index. J Am Soc Echocardiogr 2009;22:253-60. [Crossref] [PubMed]
  19. Henry A, Alphonse J, Tynan D, Welsh AW. Fetal myocardial performance index in assessment and management of small-for-gestational-age fetus: a cohort and nested case-control study. Ultrasound Obstet Gynecol 2018;51:225-35. [Crossref] [PubMed]
  20. Ma Y, Li C, Wang Y, Zhang H. Prenatal Prediction of Fetal Growth Restriction and Postnatal Outcomes by Ultrasound Assessment of Fetal Myocardial Performance Index and Blood Flow Spectrum. Evid Based Complement Alternat Med 2022;2022:4234137. Retracted Publication. [Crossref] [PubMed]
  21. Srirambhatla A, Mittal S, Vedantham H. Efficacy of Pulsatility Index of Fetal Vessels in Predicting Adverse Perinatal Outcomes in Fetuses with Growth Restriction - Differences in Early- and Late-Onset Fetal Growth Restriction. Maedica (Bucur) 2022;17:107-15. [Crossref] [PubMed]
  22. Morales-Roselló J, Bhate R, Eltaweel N, Khalil A. Comparison of ductus venosus Doppler and cerebroplacental ratio for the prediction of adverse perinatal outcome in high-risk pregnancies before and after 34 weeks. Acta Obstet Gynecol Scand 2023;102:891-904. [Crossref] [PubMed]
  23. Brown MA, Magee LA, Kenny LC, Karumanchi SA, McCarthy FP, Saito S, Hall DR, Warren CE, Adoyi G, Ishaku SInternational Society for the Study of Hypertension in Pregnancy (ISSHP). The hypertensive disorders of pregnancy: ISSHP classification, diagnosis & management recommendations for international practice. Pregnancy Hypertens 2018;13:291-310. [Crossref] [PubMed]
  24. Mecacci F, Romani E, Clemenza S, Zullino S, Avagliano L, Petraglia F. Early Fetal Growth Restriction with or Without Hypertensive Disorders: a Clinical Overview. Reprod Sci 2024;31:591-602. [Crossref] [PubMed]
  25. Nirupama R, Divyashree S, Janhavi P, Muthukumar SP, Ravindra PV. Preeclampsia: Pathophysiology and management. J Gynecol Obstet Hum Reprod 2021;50:101975. [Crossref] [PubMed]
  26. Turbeville HR, Sasser JM. Preeclampsia beyond pregnancy: long-term consequences for mother and child. Am J Physiol Renal Physiol 2020;318:F1315-26. [Crossref] [PubMed]
  27. Flanagan MF, Vollgraff Heidweiller-Schreurs CA, Li W, Ganzevoort W, de Boer MA, Vazquez-Sarandeses A, Turan OM, Bossuyt PM, Mol BWJ, Rolnik DL. Added prognostic value of Doppler ultrasound for adverse perinatal outcomes: A pooled analysis of three cohort studies. Aust N Z J Obstet Gynaecol 2023;63:19-26. [Crossref] [PubMed]
  28. Jain A, Sharma KA, Dadhwal V, Perumal V. Role of myocardial performance index (MPI) and cerebro-placental ratio (CPR) in predicting adverse perinatal outcome. Echocardiography 2022;39:1563-70. [Crossref] [PubMed]
  29. Nguyen TTN, Kotani T, Imai K, Ushida T, Moriyama Y, Kobayashi T, Niimi K, Sumigama S, Yamamoto E, Vo VD, Le MT, Le LH, Nguyen DN, Nguyen VQH, Truong QV, Cao NT, Kikkawa F. Assessment of myocardial performance index in late-onset fetal growth restriction. Nagoya J Med Sci 2021;83:259-68. [PubMed]
  30. Tan CMJ, Lewandowski AJ. The Transitional Heart: From Early Embryonic and Fetal Development to Neonatal Life. Fetal Diagn Ther 2020;47:373-86. [Crossref] [PubMed]
  31. Turgut E, Özdemir H, Turan G, Bayram M, Karcaaltincaba D. Comparison of cardiac morphology and function in small for gestational age fetuses and fetuses with late-onset fetal growth retardation. J Perinat Med 2022;50:391-7. [Crossref] [PubMed]
  32. Vasciaveo L, Zanzarelli E, D'Antonio F. Fetal cardiac function evaluation: A review. J Clin Ultrasound 2023;51:215-24. [Crossref] [PubMed]
  33. Giabicani E, Pham A, Brioude F, Mitanchez D, Netchine I. Diagnosis and management of postnatal fetal growth restriction. Best Pract Res Clin Endocrinol Metab 2018;32:523-34. [Crossref] [PubMed]
  34. Mecacci F, Avagliano L, Lisi F, Clemenza S, Serena C, Vannuccini S, Rambaldi MP, Simeone S, Ottanelli S, Petraglia F. Fetal Growth Restriction: Does an Integrated Maternal Hemodynamic-Placental Model Fit Better? Reprod Sci 2021;28:2422-35. [Crossref] [PubMed]
  35. Huluta I, Wright A, Cosma LM, Hamed K, Nicolaides KH, Charakida M. Fetal Cardiac Function at Midgestation and Subsequent Development of Preeclampsia. J Am Soc Echocardiogr 2023;36:1110-5. [Crossref] [PubMed]
  36. Sonaglioni A, Lonati C, Lombardo M, Rigamonti E, Binda G, Vincenti A, Nicolosi GL, Bianchi S, Harari S, Anzà C. Incremental prognostic value of global left atrial peak strain in women with new-onset gestational hypertension. J Hypertens 2019;37:1668-75. [Crossref] [PubMed]

(English Language Editor: L. Huleatt)

Cite this article as: Peng Y, Feng W, Yue S, He Y, Liao X, Wei Z, Gan L, Zhang J. Diagnostic value of the myocardial performance index and doppler parameters in detecting fetal growth restriction in pregnancies complicated by hypertensive disorders. Quant Imaging Med Surg 2026;16(5):346. doi: 10.21037/qims-2025-2056

Download Citation