Introduction
Neonatal asphyxia is the primary cause of neonatal hypoxic-ischemic encephalopathy (HIE), a condition characterized by hypoxic and ischemic brain damage [1]. For newborns afflicted, it is a primary cause of neurological problems and permanent impairment [2]. The prevalence of HIE is 1–8 for every 1,000 live births in affluent nations, while it is 26 for every1,000 live births in underdeveloped countries [3]. The conventional therapy for hypothermia (HIE) in high-income nations, induced hypothermia, is less successful among low-income populations, who have the largest burden of illness [4]. Thus, for neonates with HIE, early identification and effective treatment strategies are therefore critically essential.
A class of tiny noncoding RNAs known as microRNAs (miRNAs) have significant regulatory effects on a broad range of biological activities, including cell division, invasion, migration, and proliferation [5]. Emerging data indicates that dysregulation of miRNAs is typically present in human illnesses [6]. These abnormal miRNAs may both accelerate the onset of illness and serve as biomarkers for the detection and treatment of illness [7]. Additionally, functional miRNAs, such as miRNA-210, have been discovered to be essential components in the development and progression of neonatal HIE [8], also, miRNA-17-5p [9], and miRNA-204 [10].
In a recent research, O'Sullivan examined the changes in miRNA expression in umbilical cord blood from newborns suffering from HIE. In entire blood samples, one of the dysregulated miRNAs was miRNA-410 [11]. Furthermore, miRNA-410 has been shown to play a protective effect in Parkinson disease against brain damage [12], and anesthesia-induced cognitive dysfunction [13]. The biological role and clinical importance of miR-410 in newborn HIE, however, are still completely unclear.
Numerous investigations aimed to assess expression level and diagnostic efficacy of miRNA-410 in neonates with HIE to enhance the diagnosis process. Furthermore, Su et al. [13] created an oxygen and glucose deprivation (OGD)-induced cell damage model in PC12 and SH-SY5Y cells, which is the most widely used in vitro model for HIE to detect the biological function of miR-410 in controlling neuronal cells' survival [14].
Meng et al. [14] demonstrated that serum miRNA-410 expression was considerably lower in OGD-injured cell models and HIE neonates. The upregulation of miRNA-410 in PC12 and SH-SY5S cells reversed the effects of OGD-induced reduced cell viability, increased apoptosis of the cells and triggered neuroinflammation. Phosphatase and tensin homolog (PTEN) was suggested as miRNA-410's immediate target. It was shown that miRNA-410 was deregulated in serum in HIE and it functions as a potential indicator for diagnosis and improves vitality of cells in OGD-damaged cells by blocking cellular death via targeting PTEN. Thus, this study aimed to study the role of microRNA-498 and microRNA-410 in neonatal HIE and their role in controlling and prevention of neonatal encephalopathy.
Methods
This study was done with the cooperation between the Medical Biochemistry and Molecular Biology department and the neonatal intensive care unit (NICU) of Menoufia University Hospitals.
The Menoufia University Ethics Committee approved the study, which complies with the Helsinki Declaration (IRB:12/2023 PEDI 116). Prior to their enrollment, participants provided written consent.
1. Study design
This work included 60 neonates divided into 2 groups: group 1, 30 full-term neonates with HIE; group 2, 30 clinically healthy full-term neonates without any proof of neonatal HIE; matched for age and sex with the cases.
2. Inclusion criteria
1) Study group: Both sex full-term newborns exhibiting signs and symptoms of neonatal HIE based on clinical Sarnat staging [15].
2) Control group: Full-term neonates without any signs of HIE.
3. Exclusion criteria
We excluded neonates with congenital infection, probable inborn metabolic problems, perinatal hypoxia, congenital malformations, chromosomal abnormalities, preterm neonates, infant born to diabetic mothers.
Prior to the collection of blood samples, all parents provided written agreement, which was approved by the Menoufia University research ethics and human rights commission.
Every patient was exposed to taking a thorough history including prenatal, natal and postnatal history, comprehensive clinical assessment with special focusing on clinical signs of HIE in the form of: (1) respiratory dysfunction, including retracted intercostal, apnea, and elevated oxygen needs. (2) circulatory dysfunction including inadequate peripheral circulation, hypotension, tachycardia, shock and extended capillary refill. (3) Using the modified Sarnat score, the degree of encephalopathy, if any, will be determined 24 hours after delivery. (4) Additionally, on day 3 and at discharge, standardized neurologic examination was carried out.
Routine investigations include complete blood count (CBC), C-reactive protein (CRP), liver and kidney function tests.
4. Specific investigations
Assessment of serum miRNA-410 and miRNA-498 levels by quantitative real-time polymerase chain analysis (qRT-PCR).
5. Blood sample collection
Umbilical cord blood samples were obtained from all neonates in this study; The Tempus Blood RNA tubes were filled with 3 mL of cord blood and bio banked at -80C till RNA extraction.
6. RT-PCR
1) RNA extraction
With a miRNeasy kit (QIAGEN), total RNA including miRNAs was extracted. Once purification of microRNA the quantified by NanoDrop N50 nanophotoemter Implen GmbH and Implen,Inc.Schatzbogen 5281829 Munich, Germany by measuring the ratio of absorbance at 260/280 nm to estimate both RNA concentration and purity. The RNA extract was stored at -80°C.
2) Reverse transcription and cDNA production
Using the miScript II RT kit (QIAGEN), reverse transcription was used to produce cDNA. Twenty microliter of reaction mixture (4 μL of miScript HiSpec RT buffer, 2 μL of miScript Nucleics Mix, 2 μL of miScriptTM reverse transcriptases, 2 μL of nuclease-free H2O, and 10 μL of pure miRNA) were used to complete the reaction on ice. In order to suppress the reverse transcriptase enzyme, the reaction was preceded by one cycle of 37°C for 60 minutes and then 95°C for 5 minutes in a 2720 Applied Bio-systems thermal cycler (Singapore). The cDNA that was produced was stored at -20°C until the real-time PCR phase. Using a miScript SYBR Green PCR kit (QIAGEN).
3) Real-time PCR
Real-time PCR was performed. cDNA was diluted 1:5 with nuclease-free H2O prior to reaction processing, and a net volume of 25 μL (12.5 μL of SYBR Green Master Mix, 3.5 μL of nuclease-free water, 4 μL of diluted cDNA, 2.5 μL of miScript universal primer, and 2.5 μL of miScript primer assay) was employed. As a reference gene, U6 was amplified for normalization. The following primers were used; mature miR-410 AGGUUGUCUGUGAUGAGUUCG and miR 498: UUUCAAGCCAGGGGGCGUUUUUC and as a reference gene, U6 was amplified for normalization (mi Script primer assay kit, QIAGEN) Forward primer: GTGCTCGCTTCGGCAGCA Reverse primer CAAAATATGG AACGCTTC
Analysis of data was accomplished Using the ABI7500 Real-Time PCR apparatus with software version 2.0.1 and the subsequent cycle parameters: The first activation stage took place for 15 minutes at 95°C followed by 40 cycles of 3-step cycling of denaturation at 94°C for 15 seconds then, for 30 seconds, primer annealing at 55°C, followed by primer extension at 70 °C for 30 seconds. miR-410 and miR-498 expression levels were compared to U6 expression levels, and relative expression values computed with the 2−ΔΔCt technique. Melting curve analysis was used to verify the specificity of the amplification and the lack of primer dimers for each run.
6. Statistical analysis
The computer was given data, and IBM SPSS Statistics ver. 22.0 (IBM Co.). Numbers and percentages were used to describe the qualitative data. To confirm that the distribution was normal, the Shapiro-Wilk test was performed. The terms range (minimum and maximum), mean, standard deviation, median, and interquartile range were used to characterize quantitative data. The 5% level was used to assess the results' significance. The tests that were employed included the receiver operating characteristic curve (ROC), Student t test, Mann-Whitney U test, Fisher exact or Monte Carlo correction, and chi-square test.
Results
Our results on the demographic data cleared that, in studied cases group the male was more susceptible to HIE than the female neonates. Also, the gestational age among studied cases was lower than that of the normal healthy baby. While, the body weight of the studied cases was lower than the body weight of normal healthy baby (Table 1).
While our results on the obstetric characters cleared that, the maternal age of studied patients was less than that of the normal healthy baby and the parity number in patient cases was 8 (26.70%) and 22 (73.30%) for primiparous and multiparous, respectively with a mean value of 2.67±1.45 while, in control group were 6 (20 %) and 24 (80 %) for primiparous and multiparous, respectively with a mean value of 2.47±1.14. while, the number of babies was 1.63±1.35 and 2.03±1.0 for patient and control group, respectively (Table 1).
The mode of delivery in studied cases was 15 (50%) and 15 (50%) for cesarean section (CS) and vaginal delivery in patient group and in control group was 21 (70%) CS and 9 (30%) vaginal delivery. There was obstructed labor in 21 (70%) of cases while the labor was not obstructed in 100% of controls (Table 1).
Regarding the conscious level, 100% of control neonates were conscious, while, in studied cases the conscious percent was 66.70 % and those who were no conscious were 33.30%. While, the muscle tone of normal level in studied cases was 43.3% and in controls was 100 %. The atonia appears only in studied cases (16.70%) and also hypotonia appears only in studied cases (40%). The moro reflex in studied cases was 33.3 % and in control group was 100%. The respiratory distress appears only in 26.70 % of studied cases (Table 2).
The CBC (hemoglobin [Hb], white blood cells [WBCs], platelets) levels differ significantly (P<0.01) among the patient and control group. The Hb level in examined cases showed a lower level than its level in control group (12.95±2.39 vs. 14.19±0.73). The WBCs (×10³/μL) level in examined cases showed a higher level than its level in control group (16.43±6.32 vs. 13.31±1.74). The platelets (×10³/μL) level in examined cases showed a lower level than its level in control group (141.8±93.27 vs. 297.7±75.0) (Table 3).
The serum sodium level was significantly lower among the cases than controls (P<0.001) (131.5±6.78 vs. 138.7±4.08). The level of serum calcium level was significantly lower among the cases than controls (P<0.001) (8.48±0.65 vs. 9.58±0.47) (Table 3).
The CRP level was significantly higher among the cases than controls (P=0.001), (6.41±1.88 vs. 4.80±1.49). The urea level was significantly higher among the cases than controls differ (P<0.001) (59.83±28.92 vs. 24.13±8.17). The creatinine level also, was significantly higher among the cases than controls (P<0.001) (1.71±0.88 vs. 1.16±0.26) (Table 3).
The alanine aminotransferase (ALT) level was significantly higher among the patient group than control group (P<0.001) (66.33±34.84 vs. 30.27±4.95). The aspartate aminotransferase (AST) level differs significantly among the patient and control group (P<0.001), where its level in patient group was 52.97±31.46 and in control group was 20.87±2.96 (Table 3).
The arterial blood gases shown marked metabolic acidosis reached to be statically significant with PH 7.1±0.05 in cases versus control 7.37±0.03 (P<0.001), also mean HCO3 level was 12.01±2.60 in cases while 21.23±2.18 in control with (P<0.001) (Table 3).
The miRNA-410 level differs significantly among the patient and control group (P=0.027), where its level in patient group was 1.56±6.43 and in control group was 0.58±0.60.
The miRNA-498 level was significantly higher among the studied cases than controls (P=0.015), (55.63±118.24 vs. 3.74±7.09) (Table 4).
The ROC curve for miRNA-410 cleared that, the area under the curve (AUC) was 0.666 with sensitivity of 70% and specificity was 60%, the cutoff point ≤0.242, while the positive predictive value (PPV) was 63.60 and negative predictive value (NPV) was 66.70. Also, the results of the ROC curve for miRNA-498 cleared that, the AUC was 0.683 with sensitivity of 70% and specificity was 66.67%, the cutoff point >1.854, while the PPV was 67.70 and NPV was 69.00 (Figs. 1 and 2; Table 5).
The miRNA-498 was significantly positive correlated with CRP in cases (Table 6).
Discussion
Neonatal HIE causes long-term neurologic morbidity and is linked to significant newborn mortality [16]. The only known therapy for neonatal HIE at present time is therapeutic hypothermia, however it must be administered within 6 hours of delivery and is not recommended in situations of severe HIE [17]. Finding new biomarkers for diagnosis in this population might help forecast brain damage, distinguish newborns with HIE from healthy babies or those who have low-cord pH, and support doctors in making decisions in the moment [2].
Our results showed that the obstructed labor was found in 70% (21 patients) of cases versus 0% in control groups.
These results agreed with those of Johnston et al. [18] who stated that asphyxia leading to brain ischemia and hypoxia are the fundamental physiological mechanisms that cause HIE in both preterm and term neonates. A chain of reactions, that includes acidosis, the release of inflammatory mediators, and the creation of free radicals, are brought on by hypoperfusion combined with hypoxia. These biological compounds cause widespread brain damage and lack of normal cerebral autoregulation. The degree of brain maturation, length, and severity of hypoxia all affect the precise kind of damage. Myelinated fibers are more metabolically active in term newborns, making them more susceptible to HIE.
Our results on the maternal diseases and maternal drugs cleared that, the most important maternal diseases include preeclampsia, followed by diabetes mellitus and polyhydramnios and the mothers that take drugs were 11 (36.70%) and those not take drugs were 19 (63.30%).
The Apgar level at 5 and 9 minutes in examined cases was lower than its level in control healthy baby. These results attributed to the abnormal electroencephalographic readings that may indicate a poor prognosis, such as long-term neurological consequences or approaching mortality.
The results [19,20] of were in agreement with our findings, which indicated that low Apgar scores (bradycardia, inadequate respiratory effort, hypotonia, reduced alertness, weak or absent cry, aberrant skin color) and metabolic acidosis in cord blood were possible in HIE neonates. Seizures often start to occur in the first 24 hours of life for the baby. Spastic cerebral palsy in children with periventricular leukomalacia can manifest as diplegia, quadriplegia, or hemiplegia. Subcortical white matter involvement results in profound mental disability and visual impairment. Extrapyramidal symptoms are caused by involvement of the thalamus and basal ganglia. Quadriplegia, bulbar and choreoathetoid symptoms, microcephaly, and mental retardation are all linked to multicystic encephalopathy.
While, our results on the different studied parameters cleared that, the conscious level, muscle tone, moro reflex, were lower in neonates suffering from neonatal HIE than the control group and the atonia, hypotonia, Res. Distress appear only in studied cases.
These results agreed with the results of [21] where they reported that, the main symptoms of neonatal HIE include seizures, coma and hypotonia. The results of CBC cleared that, the Hb and platelets levels decreased in neonatal HIE than the control group while, the WBCs level in examined cases showed a higher level than its level in control group.
These results agreed with the results of Lelubre et al. [22] who found that severe Hb deficiency in neonatal HIE causes blood flow of the brain and oxygen saturation of the arteries to directly correlate with brain oxygen delivery. They also found that a significant decrease in Hb may result in reduced oxygen supply to the brain and ultimately hypoxia of the tissues if compensating systems intended to maintain sustained oxygenation of the tissue fail or become overwhelmed. prenatal anemia is one of the factors that contribute to mild to severe prenatal asphyxia. Also, Kalteren et al. [23] showed that in severely anemic asphyxiated newborns, a lower initial Hb level was a significant predictor of suboptimal neurodevelopmental outcome.
It has been demonstrated that the duration of fetal bradycardia affects the rising level of WBCs linked to lymphocyte levels in neonates. The number of lymphocytes increased when fetal bradycardia lasted more than 25 minutes, but these values were only temporary since they quickly returned to normal between 18 and 24 hours, which limited their applicability as a diagnostic for asphyxia. This fluctuation in the number of lymphocytes has been linked to a stress reaction that might start in the thymus [24].
Our results on the electrolytes cleared that, the serum sodium and calcium levels decreased in HIE than the control group and the potassium level increased than the control group [25].
The CRP, urea and creatinine levels increased in neonatal HIE than that of control healthy baby. Also, the random blood glucose level increased in studied cases than the control healthy baby.
These results agreed with the results of Alsulaimani et al. [26] who stated that brain inflammatory cytokines are more quickly expressed when cerebral hypoxia-ischemia occurs, and this triggers a reaction of inflammatory cells. According to research, HIE was not always associated with a rise in markers of inflammation, including CRP [27], which is consistent with our study's findings that only 15.8% of patients had high CRP levels.
Also, the ALT and AST increased in studied cases than the control healthy groups. The increasing level of AST and ALT attributed to the injury of the liver resulted from hypoxia resulted from neonatal HIE.
These results agreed with the results of Choudhary et al. [28], who revealed that, any system in the body can be harmed by hypoxia. When the fetus is insulted by hypoxicischemic conditions, a sequence of reflexes and actions take place to safeguard vital organs (brain, adrenal glands, heart) and adjust cardiac output at expense of others (kidneys, liver, gastrointestinal system, lungs, spleen).
Recent researches have indicated that miRNAs have important functions in the emergence and advancement of disorders connected to brain damage [29].
The miRNA-410 results cleared that, its level in cases was greater than the controls where its level in cases was 1.56±6.43 and in control group was 0.58±0.60.
These findings were in line with those of O'Sullivan, who examined the alterations of miRNAs expressions in cord blood in newborns suffering from HIE. Among the deregulated miRNAs in whole blood samples is micro RNA-410 (miR-410) [11]. Furthermore, it has been shown that miR-410 guards against brain damage in Parkinson disease [12], anesthesia-induced cognitive dysfunction [13] and ischemic stroke [3].
Also, our results are in line with the findings of [12,13], who showed that HIE neonates' blood levels of miR-410 were downregulated in comparison to healthy controls. Furthermore, the expression of miR-410 between babies with varying degrees of HIE was much different. Therefore, we hypothesized that miR-410 may have a part in the onset and development of newborn HIE.
Low levels of miR-498 expression were seen in ovarian and non-small cell lung cancer [30].
Our results on the 14-miRNA-498 among the patient and control group, where its level in patient group was 55.63±118.24 and in control group was 3.74±7.09.
These results aligned with the findings of Matamala et al. [31] who found miR-498 overexpression in triple negative breast cancer (TNBC) cell lines based on qRT-PCR studies and documented upregulation of miR-498 in TNBC tissues based on microarray results. Furthermore, compared to primary medullary thyroid cancer, miR-498 is substantially greater in metastatic medullary thyroid carcinoma [32].
Additionally, our findings corroborated those of Kasiappan et al. [33], who reported the variability of miR-498 expression patterns across several organs. Furthermore, reports have indicated that miR-498 hits other targets besides PTEN. For example, in an estrogen receptor-α- dependent way, telomerase reverse transcriptase promotes cell proliferation. Vitamin D-induced miR-498 overexpression, which targets telomerase reverse transcriptase mRNA, functions as a tumor suppressor and decreases telomerase reverse transcriptase levels in ovarian cancer cells.
Hypoxic stress regulates the expression of an expanding but specific subset of miRNAs, termed hypoxamirs. Although the specific miRNA hypoxic signature can vary based on the cellular or physiological scenario, a core group of hypoxamirs appears to be modulated consistently by hypoxia in diverse contexts, one of them is microRNA498. Among these, multiple hypoxamirs directly target important gene transcripts that coordinate metabolic reprogramming, DNA repair, apoptosis, and angiogenesis, among many other cellular adaptations to low oxygen availability [34].
The outcome of the children cleared that, discharged babies were 20 (66.70%) and the died babies were 10 (33.30 %). High newborn mortality and long-term neurologic morbidity are linked to ischemic brain damages mostly induced by perinatal hypoxia, which is also responsible for the high mortality from HIE [16].
The ROC curve for miRNA-410 to discriminate patients cleared that, the AUC was 0.666 with sensitivity of 70% and specificity was 60%, the cutoff point ≤0.242, while the PPV was 63.60 and NPV was 66.70. Also, the results of the ROC curve for miRNA-498 to discriminate patients cleared that, the AUC was 0.683 with sensitivity of 70% and specificity was 66.67%, the cutoff point >1.854, while the PPV was 67.70 and NPV was 69.00. These results indicated that miRNA-410 and miRNA-498 can be used as an auxiliary diagnostic and prognostic tool in HIE.
In 2024, Ichiro Wakabayashi et al. [35] found that, there were significant differences in serum and plasma levels of about one-third of the miRNAs (n=299) at time 0. Serum levels of 249 miRNAs were significantly higher than their plasma levels, while plasma levels of 50 miRNAs were significantly higher than their serum levels. Some of these differences were speculated to be due to clot formation during preparation of serum since miRNA-containing blood cells are included in the clot
In conclusion, the male was more susceptible to neonatal HIE than the female baby. MiRNA-410 and miRNA-498 can be used as an auxiliary tool in the diagnosis and prognosis of HIE.
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