- Research article
- Open Access
- Open Peer Review
Prognostic value of early, conventional proton magnetic resonance spectroscopy in cooled asphyxiated infants
BMC Pediatrics volume 18, Article number: 302 (2018)
Neonatal hypoxic-ischemic encephalopathy (HIE) commonly leads to neurodevelopmental impairment, raising the need for prognostic tools which may guide future therapies in time. Prognostic value of proton MR spectroscopy (H-MRS) between 1 and 46 days of age has been extensively studied; however, the reproducibility and generalizability of these methods are controversial in a general clinical setting. Therefore, we investigated the prognostic performance of conventional H-MRS during first 96 postnatal hours in hypothermia-treated asphyxiated neonates.
Fifty-one consecutive hypothermia-treated HIE neonates were examined by H-MRS at three echo-times (TE = 35, 144, 288 ms) between 6 and 96 h of age, depending on clinical stability. Patients were divided into favorable (n = 35) and unfavorable (n = 16) outcome groups based on psychomotor and mental developmental index (PDI and MDI, Bayley Scales of Infant Development II) scores (≥ 70 versus < 70 or death, respectively), assessed at 18–26 months of age. Associations between 36 routinely measured metabolite ratios and outcome were studied. Age-dependency of metabolite ratios in whole patient population was assessed. Prognostic performance of metabolite ratios was evaluated by Receiver Operating Characteristics (ROC) analysis.
Three metabolite ratios showed significant difference between outcome groups after correction for multiple testing (p < 0.0014): myo-inositol (mIns)/N-acetyl-aspartate (NAA) height, mIns/creatine (Cr) height, both at TE = 35 ms, and NAA/Cr height at TE = 144 ms. Assessment of age-dependency showed that all 3 metabolite ratios (mIns/NAA, NAA/Cr and mIns/Cr) stayed constant during first 96 postnatal hours, rendering them optimal for prediction. ROC analysis revealed that mIns/NAA gives better prediction for outcome than NAA/Cr and mIns/Cr with cut-off values 0.6798 0.6274 and 0.7798, respectively, (AUC 0.9084, 0.8396 and 0.8462, respectively, p < 0.00001); mIns/NAA had the highest specificity (95.24%) and sensitivity (84.62%) for predicting outcome of neonates with HIE any time during the first 96 postnatal hours.
Our findings suggest that during first 96 h of age even conventional H-MRS could be a useful prognostic tool in predicting the outcome of asphyxiated neonates; mIns/NAA was found to be the best and age-independent predictor.
Perinatal asphyxia and consequential hypoxic-ischemic encephalopathy (HIE) remains one of the leading causes of perinatal brain injury, affecting more than two million neonates yearly worldwide . Although full recovery is possible, HIE can also lead to permanent mental or psychomotor disability .
Currently, therapeutic hypothermia is the one and only neuroprotective method proven effective to reduce mortality and long-term morbidity in HIE . However, mortality or moderate to severe developmental delay still affects over 40% of cooled infants, demanding future therapeutic approaches additional to hypothermia [4, 5]. In theory, the key to successful neuroprotection is the earliest possible initiation regardless of the therapy chosen . This in turn requires proper and timely diagnosis and early establishment of prognosis .
This underscores the need for an appropriate and as-early-as-possible prognostic tool for the selection of infants who are most likely to suffer moderate to severe disability and would thus benefit from future personalized neuroprotective protocols.
Proton magnetic resonance spectroscopy (H-MRS) is one of the tools proposed for such a biomarker . This examination is becoming increasingly widespread in various medical fields, i.e. tumor diagnosis or neurodegenerative diseases. H-MRS usually accompanies brain magnetic resonance imaging (MRI) scans, and is capable of registering the spectra of various metabolites present in the examined volume of interest (VOI). Since water is the molecule most abundantly present in brain tissue, its acquired spectrum would be several orders of magnitude higher than those of other metabolites; consequently, acquisition of H-MRS requires suppression of the water signal. This can be achieved by several acquisition protocols . The analysis of the acquired spectrum informs the clinician of the metabolic state of the examined tissue, providing valuable functional information in a non-invasive way. To acquire motionless images during brain MR scans, most infants require sufficient sedation and intravenous access, not all; however, no administration of contrast material is necessary.
Several studies investigated the prognostic power of H-MRS in neonatal asphyxia, between 4 h and 46 days of age [10,11,12,13,14,15,16,17,18,19], often covering a wide age range, given the need for earliest possible prognosis.
Establishing the reproducibility of H-MRS as a prognostic biomarker also poses a problem , as previous studies used a wide range of data-optimizing equipment, software, or absolute quantification approaches to improve data quality. Taken together, there is no universal agreement regarding how H-MRS should be applied in the daily clinical practice.
The purpose of our study was to determine the prognostic value of a completely conventional H-MRS sequence (i.e. without special equipment and post-processing techniques other than basic vendor-provided analysis), performed before the 96th hour of life in infants with HIE, analyzing various metabolite ratios, their age-dependence and association with long-term neurodevelopmental outcome.
In our retrospective descriptive analysis, we reviewed all 283 patients with suspected HIE born between January 2006 and December 2010 and admitted to the regional cooling center, the Neonatal Intensive Care Unit (NICU) of the 1st Department of Paediatrics, Semmelweis University, Budapest, Hungary.
From this patient pool, we only included patients who (A) fulfilled the diagnostic criteria for moderate to severe HIE according to the international TOBY trial , being as follows: (i) at least one of the following: continued need for resuscitation/ventilation at 10 min after birth, OR Apgar score ≤ 5 at 5 min after birth OR pH < 7.0 or BE ≤ − 16 mmol/L within 60 min after birth AND (ii) altered level of consciousness (lethargy, stupor or coma) AND hypotonia or abnormal reflexes or seizures AND (iii) abnormal brain background activity registered on amplitude-integrated electroencephalography (aEEG). Additional inclusion criteria were (B) brain H-MRS scan performed before the 96th postnatal hour AND (C) having a neurodevelopmental follow-up examination using the Bayley Scales of Infant Development II between 18 and 26 months of age, as detailed below OR death (< 28 days of age OR > 28 days associated with HIE).
We excluded all patients who (a) had other underlying conditions, which could be responsible for encephalopathy besides asphyxia (i.e. stroke, intracranial hemorrhage, congenital malformation or metabolic disease). As only early onset (< 6 postnatal hours) hypothermia treatment was thought to be neuroprotective at the time of the study, we excluded patients who (b) did not receive hypothermia treatment due to delayed admission. Further exclusion criteria were: (c) gestational age < 36 weeks and (d) low quality brain H-MRS.
Altogether, 51 patients met inclusion criteria and were included in the analysis (Fig. 1).
Whole-body hypothermia treatment was initiated as soon as possible but within 6 h after delivery, using a water-filled mattress (Tecotherm©; TecCom, Halle, Germany). The target rectal temperature was between 33 and 34 °C, maintained for 72 h. In the rewarming phase, temperature increase velocity was 0.5 °C/h. All infants were ventilated throughout the cooling and rewarming phase.
Continuous morphine (Morph. hydrochlor. 10 mg/mL; TEVA Magyarország Zrt., Gödöllő, Hungary) sedation (10 μg/kg BW/h) was started following the loading dose (0.1 mg/kg BW) administered when the cooling was initiated. Phenobarbitone (Gardenal 40 mg; Aventis, Maisons-Alfort, France, 20 mg/kg BW) was given as the first line of anticonvulsant therapy if clinical or electrophysiological seizures were detected. In case of noncontrolled seizures, the phenobarbitone loading dose was repeated, or midazolam (Midazolam Torrex 5 mg/ml; Chiesi Pharmaceuticals GmbH, Vienna, Austria) was given in single or repeated doses (0.1 mg/kg BW) or in continuous infusion (0.1 mg/kg BW/h). In some cases, newborns received lidocain, phenytoin, diazepam or chloral hydrate alternatively, according to the attending clinician’s decision.
The severity of encephalopathy was determined based on a combination of aEEG background activity at 6 h of age and Sarnat staging at admission . Infants with abnormal aEEG pattern by 6 h of age (burst suppression (BS), low voltage (LV) or flat trace (FT)) OR meeting Sarnat stage 3 criteria were considered having severe encephalopathy. A normal aEEG pattern (continuous normal voltage (CNV) or discontinuous normal voltage (DNV)) AND Sarnat stage 1–2 constituted moderate encephalopathy.
Proton MR spectroscopy studies were carried out on a 3 Tesla Philips Achieva MRI scanner (Philips Medical Systems, Best, The Netherlands), at the MR Research Center of Semmelweis University, as early as the infant reached clinical stability and was suitable for transport. All MR scans were performed between 6th and 96th postnatal hours (median 25th postnatal hour). The Neonatal Emergency & Transport Services of the Peter Cerny Foundation provided the neonatal transport and the critical care, including hypothermia treatment. For the time of the examination, the infants were removed from the incubator and received continuous morphine sedation. In case of intubated infants, skilled personnel provided manual ventilation with an AMBU bag throughout the MR examination. Continuous monitoring of transcutaneous oxygen saturation and capnography was provided for all neonates during the MR scan, using Medrad Veris MR Monitoring System (Bayer Healthcare LLC, Whippany, NJ).
Patients enrolled did not undergo procedures or interventions for the purposes of the study. Brain MRI and H-MRS are part of routine diagnostic imaging in our unit as a center practice, and are performed on all neonates with suspected moderate-to-severe HIE. Use of these imaging tools aid in confirming the diagnosis, determining the timing of and nature of the hypoxic-ischemic insult (chronic intrauterine or intrapartum), and ruling out other etiologies. Finally, H-MRS measurements are not used to redirect clinical care of infants with HIE.
MR spectra were acquired using the PRESS (Point RESolved Spectroscopy) single voxel localization sequence, at echo-times TE = 35 ms, 144 ms and 288 ms, repetition time TR = 2000, number of acquisitions NSA = 128. Duration of scan was approximatively 30 min. The analyzed VOI was a 1 × 1 × 1 cm voxel in the left thalamus of infants, localized based on gradient echo survey images acquired with TE = 5 ms, TR = 75 ms and 30° flipangle.
The most frequently determined and analyzed metabolites in the H-MRS spectra are N-acetyl-aspartate (NAA), creatine (Cr), choline (Cho), myo-inositol (mIns) and lactate (Lac).
There are different TE optima for the different metabolites, due to their acquisition-dependent signal-to-noise characteristics, e.g. the Lac’s optimum is at TE = 288 ms, while for mI either TE = 35 ms or TE = 144 ms suffices. We recorded peak height, and peak area for all the above-listed metabolites (Fig. 2).
MR data analysis
We used the vendor-provided data-processing software on the MR console for analysis without any specific equipment or tool for data-optimization, in order to obtain results applicable to a general clinical setting. In order to reproduce basic, non-research center hospital level circumstances, no data-optimizing equipment or further post-processing methods were used to ameliorate the registered spectra.
Since we did not use absolute quantification protocols due to their high technical requirements, statistical analysis was carried out on all possible ratios of metabolite spectral peak heights and peak areas-under-curve, recorded at same TE. This resulted in the determination of overall 36 metabolite ratios (Table 1).
To improve the accuracy of our analyses, we excluded metabolite ratios derived from metabolite spectra with signal-to-noise ratio (SNR) below 1, i.e. where noise intensity exceeded signal intensity [23, 24].
Neurodevelopmental follow-up was measured by Bayley Scales of Infant Development II tool-kit, performed between 18 and 26 months of age by trained personnel, blinded to the H-MRS results. We defined poor outcome as either death (< 28 days of age OR > 28 days associated with HIE) OR moderately/severely delayed development (Mental Developmental Index (MDI) or Psychomotor Developmental Index (PDI) < 70). All other outcomes were considered as good outcome.
Categorical variables are reported as absolute numbers and percentages while continuous variables as mean ± standard deviation or median [25th to 75th interquartile range] depending on the distribution of the parameters. Shapiro-Wilk test was used to assess normality. Categorical variables were compared with the Fisher’s exact test, while continuous variables were compared with the Student t-test or Mann-Whitney U-test for parametric and non-parametric comparisons, respectively.
To select the best metabolite ratios for prognostication, a three-step statistical procedure was implemented. First, we tested the association between the metabolite ratios and outcome. To adjust for multiple testing, we used Bonferroni-correction, that is to say, due to 36 examined metabolite ratios, we considered statistical results significant at p < 0.0014 (0.05/36 = 0.0014).
Second, we considered the fact that in the early hours after hypoxic insult, the brain metabolic activity shows extreme variations in time-dependent fashion [25, 26]. Therefore, metabolite ratios measured by H-MRS may also vary significantly depending on timing of data acquisition. Considering that these metabolic changes are still not fully understood and described, we aimed to select metabolite ratios with low or no variability during the first 96 postnatal hours, in order to ensure generalizability of our results for all infants within this period, irrespective of timing of the MR examination. We tested postnatal age-dependence of metabolite ratios using Spearman rank-correlation analysis.
Third, we evaluated the prognostic performance of metabolite ratios using Receiver Operating Characteristics (ROC) curve analysis to establish the potential cut-off-value (corresponding to the highest likelihood ratio of ROC curves), as well as to determine the sensitivity, specificity, positive and negative predictive values of the proposed markers. Moreover, we compared the metabolite ratios as diagnostic tests using the area under the ROC curve (AUC) using the method described by Hanley and McNeil .
Demographic, clinical and spectral data were analyzed and plotted using the GraphPad Prism software version 6.0 (GraphPad Software Inc., San Diego, California, USA).
Fifty-one neonates with moderate-to-severe HIE met the inclusion criteria, and were enrolled in our study. Hypothermia treatment was initiated before the 6th postnatal hour for all 51 neonates, with median [IQR] 2 [1.4; 3.1] hours. Forty-five out of the 51 patients had the H–MRS examination performed while receiving whole-body hypothermia. The remaining 6 patients had the examination done before the initiation or after the completion of hypothermia treatment. Nevertheless, all scans were performed within 96 h of age.
Clinical characteristics and MRI findings of these patients are shown in Tables 2 and 3, accordingly, categorized by long-term outcome. Of the 51 patients, 16 infants were considered to have poor outcome, including the 9 patients that died in the perinatal period (i.e. first 28 days), and the 7 patients who had moderately/severely delayed development (Mental Developmental Index (MDI) or Psychomotor Developmental Index (PDI) < 70). Of these 7 patients, 4 infants were diagnosed with cerebral palsy (2 associated with mental retardation and one with epilepsy), 2 had mental retardation and one patient suffered from neuronal hearing loss and epilepsy. None of our patients died between 28 days and the follow-up examination. Good and poor outcome groups only differed significantly in their 5′ and 10′ Apgar scores, as well as occurrence of stage 3 HIE seen on MR images.
Of the 36 metabolite ratios evaluated in the first 96 postnatal hours for prognostication of good or poor neurodevelopmental outcome, 3 metabolite ratios differed significantly between the good and poor outcome groups, rendering them candidates for further analysis (Table 4): mIns/NAA height (TE = 35 ms), NAA/Cr height (TE = 144 ms) and mIns/Cr height (TE = 35 ms).
Next, we tested the age-dependence of these 3 metabolite ratios during the first 96 postnatal hours among all 51 patients, as it has been described that the brain metabolic activity shows extreme time dependent variations in the early hours after hypoxic insult. We aimed to search for a uniformly detectable metabolite ratio that would be suitable for prognostication any time during the first 4 postnatal days. Assessment of age-dependence did not show significant correlation between either of the 3 metabolite ratios and age at the H-MRS examination. All 3 metabolite ratios showed weak correlation with the timing of the examination, hence might be considered relatively stable during the first 96 postnatal hours (Fig. 3).
Finally, comparing the prognostic performance of these 3 relatively age-independent metabolite ratios, mIns/NAA height at TE = 35 ms had a better discriminative power than NAA/Cr height at TE = 144 ms and mIns/Cr height at TE = 35 ms to identify patients with good versus poor outcome (cut-off-values 0.6798, 0.6274 and 0.7798, respectively, AUC: 0.9084, 0.8396 and 0.8462, respectively, difference between ROC curves p < 0.00001). Thus, out of the 36 evaluated metabolite ratios within the first 96 h of age, mIns/NAA height at TE = 35 ms seems to give the best prediction of outcome, with 84.6% sensitivity and 95.2% specificity, irrespective of the timing of the MR examination (Fig. 4 and Table 5).
To the best of our knowledge, this preliminary study with a relatively small sample size is the first one that investigated the prognostic accuracy of conventional H-MRS examination performed during the first 4 postnatal days in a group of infants with moderate to severe HIE in the era of hypothermia treatment. We found that myo-inositol/N-acetyl-aspartate height ratio (TE = 35 ms) was the best predictor of neurodevelopmental outcome at 2 years of age. This metabolite ratio proved to have low correlation with age at MR scan during the first 4 postnatal days and showed a specificity of 95.2% and a sensitivity of 84.6% for discriminating between good and poor outcome.
Previously, several studies investigated the prognostic power of H-MRS in asphyxiated neonates using various methods, protocols and equipment [10,11,12,13,14,15,16,17,18,19]. Nevertheless, it is problematic to draw an overarching conclusion applicable for the general clinical practice, due to the difference of the methods, findings and conclusions. Indeed, a wide range of H-MRS derived metabolites were suggested as potential biomarkers, e.g. some studies concluded that absolute Lac levels and/or Lac-containing metabolite ratios (Lac/NAA, Lac/Cho, Lac/Cr) were the most accurate in prediction of outcome [11,12,13,14, 16,17,18,19], while others showed that NAA/Cr, NAA/Cho, absolute NAA and/or Cho levels had promising prognostic powers [10, 11, 15, 17, 18], but only few studies investigated glutamate (Glx) or glutamate-containing metabolite ratios (Glx/Cr) , and/or mIns .
Interpretation and generalizability of these results are hindered by the fact that there was a marked variability regarding the methods used, some studies applied various data-optimizing software [15, 18] methods for absolute metabolite quantification [14, 15], or special head-coils [14, 17] in order to ameliorate the information acquired from the metabolite spectra. These methods may indeed improve data quality; however, they are not generally applicable in standard clinical settings .
Therefore, our intent was to prove the clinical utility of conventional H-MRS sequence with vendor-provided analysis tools in the diagnostic workup of neonatal asphyxial encephalopathy.
Despite their limitations, existing evidence largely supports the use of peak areas as prognostic markers in patients with neonatal encephalopathy. A meta-analysis concluded that deep gray matter Lac/NAA peak area ratio is the most accurate predictor of adverse outcome . Based on Bottomley’s comprehensive review of MR spectroscopy  however, without post-processing techniques, the use of peak height and peak area has certain challenges. While peak height provides an acceptable measure for non-overlapping peaks, it is affected by patient motion and inhomogeneous widening of spectrum widths. Peak areas are relatively immune to motion artefacts and spectrum widening. However, since most of the integrated area of a peak resides near its base, noise and overlapping of other peaks can significantly affect the measurements. Taking these factors into consideration, we assessed the prognostic value of both peak heights and peak areas. Based on our findings, it seems that without the use of post-processing, peak height may have an appropriate predictive value and might be useful in the common clinical setting without the use of specialized imaging and post-processing techniques.
We set out to find markers that have similar or possibly even higher value for prognostication than markers published earlier.
To this end, we targeted our investigation on H-MRS scans performed the earliest possible, within 96 postnatal hours, presuming that the earlier the accurate prognostic information, the higher its clinical importance. The majority of the above-listed studies investigated H-MRS scans that were performed significantly later and in a wider range of infant age (3 to 45 days of age) [10, 11, 15,16,17,18,19], with only three papers focusing on early infant ages similar to our study [12,13,14], all three analyzing considerably small patient cohorts. One of them investigated infants during their first day of life (31 neonates of 4–18 postnatal hours); however, considering the unstable clinical status of many severely asphyxiated infants, this may be unfeasible in the clinical practice . The second paper (11 neonates of 12–48 postnatal hours) concluded that only combined H-MRS and diffusion-weighted imaging is capable of accurate prediction of outcome , while the third one (17 neonates of 48–96 postnatal hours) used absolute quantification and a custom-made head-coil to optimize data acquisition . Nevertheless, none of these early-acquisition studies examined neonates while undergoing therapeutic hypothermia.
In addition, although a recent study examined 88 infants with perinatal asphyxia who underwent therapeutic hypothermia, MR scans and H-MRS were acquired only within the first 7 postnatal days .
In the era of therapeutic hypothermia, the effect of cooling on brain metabolites is an important issue. Existing evidence suggests that hypothermia increases the clearance of lactate upon cerebral reperfusion  and increases overall lactate and myo-inositol levels in the cortex, while increasing the level of taurine and decreasing the level of choline in the thalamus . Even though further studies are needed to outline the hypothermia-induced changes in metabolites detected by H-MRS, these findings suggest that thalamic myo-inositol/N-acetyl-aspartate values are not affected by cooling.
As an essential step in our analysis, we searched for metabolite ratios independent from postnatal age at the MR examination. It is well-known that in the early hours after hypoxic insult, the brain has an extremely dynamic metabolic profile [25, 26], so theoretically, metabolite ratios measured by H-MRS may vary significantly depending on the timing of the MR examination. In addition, the timing of the MR scan is influenced by the clinical stability of newborns. Based on these considerations, the acquisition of a single cut-off value for the proposed biomarker suitable for differentiation between outcomes may be extremely complex, given that the time-dependent metabolite changes are still not fully understood and described. Subsequently, the prognostic markers that vary depending on patient age may show false negative or false positive results, if performed too early or too late in the examined time period, so would require a dynamic range of cut-off-values (cut-off-curve) which calls for considerably larger population and/or repeated measures. Conclusively, until the precise kinetics of brain metabolites are described, the cut-off-value of the proposed prognostic marker should ideally not change with time but should only be determined by severity of encephalopathy and potential outcome. None of the existing studies contemplated the possible postnatal age dependence of the observed metabolites or metabolite ratios. Therefore, we aimed to investigate the stability of metabolite ratios, and found that none of the 3 metabolite ratios associated with outcome showed correlation with timing of the examination in the investigated time window, hence could be potentially independent of postnatal age. We consider the contemplation of the time-dependence of brain metabolites as one of the strengths of our analysis, even though further dependence analyses in repeated measures and larger population are needed to confirm our findings.
Existing evidence suggests that the role of both myo-inositol and N-acetyl-aspartate is complex. Myo-inositol is a pentose sugar, precursor for inositol-derived lipid synthesis and part of the intracellular second-messenger system . To date, studies suggest that myo-inositol could be the breakdown product of abnormal cerebral inositol-polyphosphate metabolism and the cell membrane component myelin , implementing that increased myo-inositol levels signal cell death.
N-acetyl-aspartate is the second most abundant amino acid in the brain, functioning as an osmolite with multiple functions, e.g. molecular water pump for neurons to help osmotic regulation, as well as source, storage and transport of acetyl-group, aspartate and amino-nitrogen, for protein and lipid synthesis . Studies suggest that NAA levels decrease after neuronal injury or dysfunction, even in the absence of cell death .
Conclusively, neuronal injury induced by hypoxia-ischemia is considered to raise myo-inositol levels and decrease N-acetyl-aspartate levels, thus increasing myo-inositol/N-acetyl-aspartate ratio and providing scientific background for our findings.
It is surprising that none of the lactate-containing metabolite ratios met the strict significance requirements of Bonferroni-correction. One of the reasons for this finding might be the low quality of lactate spectral data. In our measurements, signal-to-noise ratio of lactate peaks were extremely low, with a median [IQR] signal-to-noise ratio of 1.0 [0.7; 1.6] without selection, and 1.6 [1.1; 2.5] after selection based on SNR = 1 criterion. However, low spectral data quality only affected peaks of lactate, since all other metabolites showed significantly more favorable signal-noise characteristics, with a median [IQR] signal-to-noise ratio of 10.8 [8.0; 12.8] for N-acetyl-aspartate, 11.9 [8.8; 14.5] for choline, 11.4 [7.3; 13.9] for creatine and 5.7 [4.8; 7.5] for myo-inositol, reflecting significantly better data quality. Based on these findings, spectral peak of lactate cannot be accurately assessed and interpreted in the general clinical setting and in the absence of post-processing techniques, despite its widespread use in previous studies.
In our study, the volume of interest was a 1 × 1 × 1 cm voxel in the left thalamus. In this cohort, only one patient presented with watershed injury in the left parieto-occipital region, and one patient with widespread cortical lesion. Due to the low prevalence of watershed lesions, we were unable to assess the prognostic value of H-MRS in this type of neuronal injury.
Our study also has a number of limitations. Even though we outlined our methodology to eliminate all possible errors, there are certain points that still might have given way to inaccuracy in our conclusions. First, our study is retrospective in nature, therefore we could not control for factors possibly affecting the findings such as the imaging process and the clinical parameters. This may be considered a limitation compared to a prospective clinical study, where imaging and clinical parameters would have been fine-tuned for the purpose of the study. On the other hand, this could be viewed as a strength from a clinical standpoint, since we had to rely on data that could have been obtained in any MR facility imaging asphyxiated neonates. Therefore, our findings might have more relevance in the general clinical practice. The small sample size of our population is another limitation decreasing the accuracy and reliability of the statistical analysis. The difference between the sizes of the outcome groups (35 good versus 16 poor) might also be considered as a limitation, as our analysis might have been underpowered. Moreover, some may criticize our approach, and may state that all neonates should be examined at the exact same age, which would enable prognostic results to be as accurate as possible. However, considering that infants cannot be assessed before reaching certain clinical stability, this would not be a realistic expectation in the clinical practice.
Obviously, our results must be verified in prospective trials on larger populations and on different MR scanners to corroborate the prognostic power of the proposed H-MRS metabolite ratios.
In summary, we propose that H-MRS performed before 96 h of age is a potentially promising tool for early prediction of outcome in asphyxiated neonates. The use of H-MRS may add valuable information for the clinicians to assess the severity of the hypoxic insult and potentially utilize additional neuroprotective therapies. Furthermore, our results suggest that even conventional H-MRS might have a high enough prognostic accuracy to be used in routine clinical practice.
Continuous normal voltage
Discontinuous normal voltage
Diffusion weighted imaging
Proton magnetic resonance spectroscopy
Mental Developmental Index
Magnetic resonance imaging
Psychomotor Developmental Index
Receiver Operating Characteristics
Volume of interest
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We would like to acknowledge the important contribution of Istvan Seri MD, PhD, HonD, Professor of Pediatrics, Children’s Hospital Los Angeles and USC Keck School of Medicine, Los Angeles, CA and Honorary Member at Hungarian Academy of Sciences, Budapest, Hungary. We would also like to acknowledge the technical contributions of Adam Gyorgy Szabo MD, MR Research Center, Semmelweis University, Budapest, Hungary.
AJ was supported by Hungarian Academy of Science, Premium Postdoctoral Fellowship (PPD460004). LRK was supported by the Bolyai Research Fellowship program of the Hungarian Academy of Sciences. The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript.
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on request.
Ethics approval and consent to participate
The study was approved by the Scientific and Medical Research Council Ethics Committee of Hungary (11790–2/2016/EKU). Consent for routine diagnostic procedures and clinical care was gained from parents or legal guardians for all the participating neonates. No additional procedures were carried out other than the routine diagnostic tests and routine clinical care of infants.
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The authors declare that they have no competing interests.
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Barta, H., Jermendy, A., Kolossvary, M. et al. Prognostic value of early, conventional proton magnetic resonance spectroscopy in cooled asphyxiated infants. BMC Pediatr 18, 302 (2018) doi:10.1186/s12887-018-1269-6
- Perinatal asphyxia
- Hypoxic-ischemic encephalopathy
- Proton magnetic resonance spectroscopy
- Conventional sequence
- Neurodevelopmental outcome