Real-time shear wave elastography evaluation of the correlation between brain tissue stiffness and body mass index in premature neonates.

BACKGROUND: Real-time shear wave elastography (SWE) is non-invasive and reliable for quantitatively evaluate stiffness of tissues and organs. Until now, little researches have applied SWE to evaluate brain tissue of premature neonates. This study sought to compare differences in the average brain tissue elasticity modulus (Emean) values of neonates, and explore the factors affecting these differences.
METHODS: In total, 159 neonates admitted from December 2019 to February 2021 were taken as the study subjects and divided into 2 groups based on their time of birth. Premature neonates, full-term neonates, and neonates with neonatal pneumonia were included in this study. Of the 159 neonates, 76 were premature and 83 were full-term. SWE was used to quantitatively evaluate the Emean of bilateral paraventricular white matter, thalamus, and choroid, and to analyze the relationship between body mass index (BMI) and Emeans in both groups of neonates.
RESULTS: The Emeans of the paraventricular white matter, thalamus, and choroid of the premature neonates were lower than those of the full-term neonates (P<0.001). The BMI of the premature and full-term neonates was positively correlated to the bilateral paraventricular white matter, thalamus, and choroid Emean.
CONCLUSIONS: SWE can be used to quantitatively evaluate the brain tissue stiffness of neonates, and as a reference for neonatal brain-related diseases. 2021 Translational Pediatrics. All rights reserved.

Introduction

Neonates are prone to intracranial hemorrhage due to their imperfect cranial brain structure, which can lead to a series of cognitive and neurological dysfunctions. Ultrasonography is non-invasive, convenient, and efficient, and is currently the main method for the clinical screening and follow-up of neonatal craniosynostosis (1). Shear wave elastography (SWE) is an ultrasonic imaging method based on detecting the propagation of shear wave in tissue (2). It can be used to quantitatively measure tissue stiffness in a region of interest (3). SWE has been widely used as an aid in ultrasound diagnoses of diseases of abdominal organs, superficial organs, and musculoskeletal nerves. Tzschätzsch et al. have published a paper demonstrated that SWE can detect acute cerebral stiffness changes induced by intracranial pressure variations in a total of 26 healthy adults (4).

Elastic modulus (Emean) which measures the resistance of the material to elastic—or “springy”—deformation (5). The elasticity of brain tissue was found to be significantly lower in the preterm group compared with the term group (6). Additionally, brain tissue elasticity has been thought to be a factor affecting brain re-expansion after the evacuation of intracranial hemorrhage (7). Furthermore, premature neonates tended to have lower elasticity of brain tissue and lower body mass index (BMI) compared with the full-term infants.

However, little research has been conducted on using SWE in the diagnosis of neonatal craniocerebral disorders. In this study, we compared the Emean of the lateral paraventricular brain white matter, thalamus, and choroid in premature and full-term neonates, and also analyzed the related factors affecting brain tissue stiffness in neonates and its association with BMI. We present the following article in accordance with the MDAR reporting checklist (available at https://dx.doi.org/10.21037/tp-21-513).

Methods

General information

The data of 159 neonates admitted to our hospital from December 2019 to February 2021 were collected. Of the 159 neonates, 76 were premature with a mean gestational age of 32.93±1.85 weeks and a body mass index (BMI) of 10.70±1.01, and 83 were full-term with a mean gestational age of 39.22±1.02 weeks and a BMI of 12.94±0.83. The neonates’ age ranged from 0 to 28 days. Premature neonates, full-term neonates, and neonates with neonatal pneumonia were included in this study. Neonates with hyperbilirubinemia, intracranial hemorrhage, ischemic-hypoxic encephalopathy, hydrocephalus, amniotic fluid contamination, or intracranial tumors were excluded from the study. All procedures performed in this study involving human participants were in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the Medical Ethics Committee of Lanzhou University Second Hospital (No.: 2021A-598) and all the guardians of the neonates gave informed consent for the neonates to participate in this study.

Instruments and methods

A color Doppler ultrasound diagnostic instrument from Supersonic Imagine Aixplorer, France with a probe frequency of SC6-1 MHz was used. The examination room was warm and comfortable, and the neonates were examined in the supine position in a quiet state. The cranial structures were observed via the fontanelle and lateral fontanelle in 2-dimensional (2D) grayscale mode, and cerebral blood flow parameters were detected in color Doppler mode. Neonates who met the above-mentioned criteria were included in the study (3).

Switching to the SWE mode, the Emeans of the affected neonate’s left/right paraventricular white matter, thalamus, and choroid were measured via a sagittal sweep of the fontanelle, and the Emeans were averaged over 3 measurements. Young’s modulus value (E=3ρc2, where E represents the tissue elastic modulus, ρ represents the tissue density, and c represents the shear wave propagation velocity) were automatically calculated by the machine (8). All procedures were performed by the same physician. A coupling agent was applied thickly during the examination; only minimal pressure was placed on the affected fontanelle. The area of interest for the Emean measurement in the paraventricular cerebral white matter was placed in the area of the cerebral white matter at the peripheral edge of the corpus callosum. The area of interest for the Emean measurement in the thalamus was placed in the middle of the thalamus. The area of interest for the Emean measurement in the choroid was placed at the head of the choroid near the caudate sulcus of the thalamus. A 3 cm × 4 cm sampling frame size was chosen to display the 3 regions of interest simultaneously and reduce the sampling time.

Statistical methods

SPSS 24.0 statistical software was used to process the data. Measures conforming to a normal distribution are expressed as mean ± standard deviation (). The t-test was used for comparisons between groups. Correlations between neonatal BMI and the Emeans of selected regions of the bilateral lateral paraventricular brain white matter, thalamus, and choroid were analyzed using Pearson’s correlation coefficient. A P value <0.05 was considered statistically significant.

The Emean measurements of the SWE sonogram for the regions of interest in the neonatal cranial lateral ventricular parietal cerebral white matter, thalamus, and choroid are shown in .

Figure 1

Emeans of multi-site regional brain tissue of the neonatal brain. (A) Lateral paraventricular white matter Emean 12.6 kPa; (B) thalamus Emean 13 kPa; (C) choroid Emean 9.5 kPa.

The Emeans of the lateral paraventricular white matter, thalamus, and choroid were lower in the premature neonate group than the full-term neonates control group (P<0.001). The Emean of the neonatal brain tissue thalamus was > lateral paraventricular brain white matter, which was > choroid (see ).

Table 1

Comparison of Emean of the neonatal brain between premature neonates and full-term neonates

Variables	Premature neonates (n=76)				Full-term neonates (n=83)
	Left (kPa)	Right (kPa)	Mean (kPa)		Left (kPa)	Right (kPa)	Mean (kPa)
Lateral paraventricular white matter	10.39±2.10a	10.23±2.08a	10.50±2.04a		12.32±2.14	12.65±2.09	12.49±1.91
Thalamus	11.14±2.33a	11.25±2.07a	11.38±2.16a		13.31±2.49	12.92±2.40	13.11±2.22
Choroid	9.18±2.19a	9.15±2.17a	9.16±2.07a		9.65±2.24	9.62±2.20	9.64±2.08

a, P<0.001 premature neonate group vs. full-term neonate group. Emean, elasticity modulus.

The Pearson’s correlation coefficient analysis showed that the neonatal lateral paraventricular brain white matter, thalamus, and choroid brain tissue stiffness values were significantly and positively correlated with BMI (P<0.05). The correlation coefficients between the lateral paraventricular brain white matter, thalamus, and choroid and BMI were r=0.457, r=0.681, and r=0.462, respectively, for the premature neonate group and r=0.476, r=0.327, and r=368, respectively, for the full-term neonate control group (see ).

Figure 2

Correlation between Young’s modulus values and BMI in the brain tissue of premature neonates. BMI, body mass index.

Figure 3

Correlation between Young’s modulus values and BMI in the brain tissue of full-term neonates. BMI, body mass index.

Discussion

The imperfect development of cranial structures in premature neonates increases the risk of cognitive impairment, neuromotor deficits, and neurodevelopmental abnormalities (9,10). In addition to being convenient and inexpensive, with the improvement of probe resolution, ultrasonography has high diagnostic value in the diagnosis of neonatal cranial diseases, and can be combined with color Doppler imaging to assess the functional status of intracranial cerebral blood flow (3,11). Ultrasonography is currently the preferred method for the routine screening of neonatal early cranial diseases. However, the clinical ultrasound examination techniques currently and commonly used are susceptible to the subjective judgment of different operators. Thus, the provision of more quantitative analysis data would improve the sensitivity and specificity of ultrasonography in neonatal cranial applications.

The SWE is an ultrasound imaging technique that has emerged in recent years. This technique acts on the acoustic radiation force emitted by the ultrasound probe in the tissue region of interest, and then measures the shear wave propagation velocity in the tissue and automatically calculates Young’s modulus value (E=3ρc2, where E represents the tissue elastic modulus, ρ represents the tissue density, and c represents the shear wave propagation velocity) (8) to quantitatively assess tissue stiffness. Currently, SWE is widely used clinically; however, its application to neonatal cranial brain research is still in the preliminary stage (6,12,13).

Neonatal central nervous system development is highly sensitive to external sources, and disturbances of the developmental process can have important effects on brain tissue structure and function (14,15). Research has been conducted on the safety of 2D-SWE in craniocerebral examinations. For example, Li et al. (12) used shear wave imaging to irradiate the cranial brains of different groups of newborn C57BL/6 rats, and found that 30 min of irradiation did not cause significant changes to the brain tissue structure of these newborn rats. However, the newborn rats showed decreased brain protein kinase Ca (p-PKCa) protein expression levels after >10 min of irradiation, and the brain phosphatidylinositol-3-kinase mammalian target of rapamycin signaling pathway was disturbed after >30 min. The results of another study (16) showed that there was no significant difference in learning and memory between experimental and control groups when the experimental rats were fed to 3 months of age, and there was no significant difference in the expression of proteins related to signaling pathways closely related to neurological development in the hippocampus and cortex of the 2 groups of rats. In the present study, the difference in the Emean data of brain tissue in the same region was small and the image display quality was high when the SWE mode of the C5-1 probe was used to measure brain tissue. Further, to reduce the total time of the ultrasound examination and thus minimize the possible biological effects that may occur during the cranial ultrasonography of neonates, the present study showed that elasticity information of brain tissue in the lateral paraventricular brain white matter, thalamus, and choroid could be simultaneously acquired when the SWE sampling frame size was 3 cm × 4 cm.

In this study, the Emean of the thalamus was > the Emean of the lateral paraventricular brain white matter, which was > the choroid in the brain tissue of both premature and full-term neonates. Few studies (6,13,16) showed that SWE can effectively measure brain tissue stiffness values in all the brain regions of neonates, and Albayrak et al. (6) proposed that the cut-off points of Young’s modulus values of lateral paraventricular brain white matter and thalamus in normal neonates were 6.59 and 8.28 kPa, respectively. Compare with the present study, both the white matter and thalamus Young’s modulus values were smaller. During the procedure in the present study, there were some differences in the measured values of brain tissue stiffness in the same region when the SWE probe frequencies were performed. Notably, the C5-1 probe in a SWE mode was used to collect the intracranial brain tissue measurements for Young’s modulus values, which has better reproducibility than the higher frequency probe used to collect data in the present study. Tavare et al. (13) showed that Young’s modulus values of the thalamus, cerebellum, and lateral paraventricular brain white matter in children with ischemic-hypoxic encephalopathy differed from those of normal full-term neonates, and suggested that SWE could provide a basis for the clinical diagnosis of brain injury. However, very few studies have examined the correlation between neonatal BMI and brain tissue elasticity values.

The gray matter of the brain is the dense site of neuronal cell bodies, and the white matter of the brain is the site of nerve fiber aggregation. When the thalamic elastic stiffness values are higher than the white matter stiffness values in the neonatal period, the gray matter structure is denser than the white matter structure of the brain. The development of the central nervous system is an extremely complex and continuous process that involves a dynamic balance between cell proliferation, differentiation, migration, synaptogenesis, myelin formation, and apoptosis of brain neurons and glia. Examinations of correlations between brain tissue stiffness and the degree of cerebral vascular development and cerebral blood perfusion pressure have shown that the denser the neuronal cells, the higher the value of brain tissue stiffness (17). In this study, we analyzed correlations between BMI and brain tissue Emeans in premature and full-term neonates, and found that the higher the BMI, the higher the neonatal thalamus, lateral paraventricular cerebral white matter, and choroid plexus tissue stiffness. Pong et al. (18) used Magnetic resonance elastography (MRE) to examine the cranial brains of rats at 1–6 weeks, and the results suggested that the brain gray matter stiffness of young rats increases with age. Which provides support for the results of the present study.

There are some advantages and disadvantages of SWE in evaluation of brain tissue stiffness. Stiffness measurements do not take a matter of minutes by SWE, and intraoperative ultrasonography is a relatively safety approach. Additionally, SWE can provide dynamic real-time images while not impacted by brain shift (19,20). Furthermore, the major flaws of using SWE to evaluate brain tissue stiffness including, stiffness values that may not be acquired when depth and/or obstacle forbid shear wave propagation, different ultrasonography operators may result in distinct results due to their different skills (19,21).

This study had a number of limitations. First, the subjects in this study were relatively mobile, regular measurements of Young’s modulus values of the brain tissue in the same sample could not be collected. Second, the examination sites in this study were limited to the detection of the Emeans of the bilateral lateral paraventricular cerebral white matter, thalamus, and choroid. Future research should collect multi-site measurements and conduct a systematic analysis of large sample size data to provide a range of brain tissue elastic stiffness values at different stages of neonatal life.

In summary, the SWE technique can be used to transcranially quantify brain tissue stiffness in premature and full-term neonates. The sample size should be expanded to establish a database of normal brain tissue stiffness values for neonates to provide a reference basis for the clinical diagnosis of neonatal craniosynostosis.

The article’s supplementary files as