Comparing the Diagnosis of White Matter Injury in Premature Newborns with Serial MR Imaging and Transfontanel Ultrasonography Findings

Steven P. Miller; Camilla Ceppi Cozzio; Ruth B. Goldstein; Donna M. Ferriero; J. Colin Partridge; Daniel B. Vigneron; A. James Barkovich

Abstract

BACKGROUND AND PURPOSE: The accurate identification of white matter injury in premature neonates is important for counseling parents and for targeting these high risk neonates for appropriate rehabilitation services. The objective of this study was to compare the diagnosis of white matter injury detected by serial MR imaging and ultrasonography of a contemporary cohort of premature neonates.

METHODS: Each of the 32 consecutively enrolled neonates was studied with MR imaging at a median postconceptional age of 31.9 weeks (range, 27.6–38.1 weeks) and again at a median postconceptional age of 36.5 weeks (range, 33.4–42.9 weeks) and with serial ultrasonography according to a clinical protocol. Because periventricular echogenicity shown on ultrasonograms evolves over time, both the highest grade of echogenicity and the grade of echogenicity shown on the last neonatal ultrasonogram were used in the analysis to determine the predictive values and correlation (Spearman’s rho) of ultrasonography for predicting white matter abnormalities shown on MR images.

RESULTS: White matter abnormalities were diagnosed in 18 (56%) neonates based on MR imaging, consisting of foci of scattered T1 hyperintensity in the periventricular white matter, and in 22 (69%) neonates based on ultrasonography, consisting of abnormal periventricular echogenicity. The severity of white matter abnormalities shown by MR imaging was not correlated with the highest grade of white matter abnormalities detected with ultrasonography (rho=0.18, P=.3) or with the grade of white matter abnormalities shown on the last ultrasonogram (rho = 0.16, P=.4).

CONCLUSION: Although ultrasonography is commonly used to screen premature neonates for white matter injury, it was not a sensitive predictor of the milder spectrum of MR imaging-defined white matter abnormalities.

Of all premature survivors of the intensive care nursery, it is estimated that 5% to 10% exhibit major motor deficits and another 25% to 50% exhibit significant developmental and visual difficulties (1–7). These deficits are classically associated with neonatal evidence of white matter injury that is typically in the centrum semiovale, optic, and acoustic radiations (1, 3–7). The identification of white matter injury is important for accurately counseling parents of premature neonates and for targeting these high risk neonates for appropriate rehabilitation services.

Ultrasonography is the primary imaging technique for the evaluation of brain injury in premature neonates. It is noninvasive, inexpensive, and portable, allowing examinations to be performed without the need to move the infant. The anterior fontanel provides a convenient sonographic window, allowing excellent noninvasive imaging of the deep midline regions of the brain. Although this allows accurate detection of cystic periventricular white matter injury, germinal matrix hemorrhage, and hydrocephalus, the ability of ultrasonography to accurately diagnose non-cystic white matter injury remains controversial (8–10).

MR imaging provides high resolution, noninvasive imaging of brain parenchyma in neonates. Compared with ultrasonography, MR imaging may better define the site, extent, and type of non-cystic white matter abnormalities in premature neonates (11–13).

The goal of the present study was to determine the spectrum of white matter injury detected by serial MR imaging and ultrasonography of a contemporary cohort of premature neonates. A second goal of the study was to then determine the correlation of abnormalities shown by ultrasonography with white matter injury diagnosed based on MR imaging. We hypothesized that MR imaging is more sensitive for detecting small abnormalities of the periventricular white matter compared with ultrasonography, whereas MR imaging and ultrasonography are similarly sensitive for detecting more severe abnormalities, such as cystic white matter injury and ventriculomegaly.

Methods

All neonates <36 weeks gestational age born in or transferred to our institution’s intensive care nursery were considered for enrollment in a prospective cohort study evaluating the detection of brain injury by MR imaging. This prospective cohort comprised a consecutive series of 32 neonates of <36 weeks gestational age who were enrolled in this study from September 2000 to March 2002 and who completed two MR imaging examinations. The inclusion criterion for this cohort was gestational age <36 weeks. Gestational age was calculated based on the last menstrual period or early sonography (<24 weeks); if the difference between the two methods was >7 days, the sonography date was used. Infants were excluded from enrollment if clinical evidence indicated a congenital malformation or syndrome, if congenital infection such as toxoplasmosis, rubella, cytomegalovirus infection, or herpes simplex infection was present; or if sonography showed evidence of large parenchymal hemorrhagic infarction (grade IV hemorrhage). Our institution’s Committee on Human Research approved the protocol. Infants were studied only after voluntary informed consent was obtained from parents.

Imaging Techniques

Each of the 32 neonates, with a median postconceptional age of 29 weeks (range, 24.7–32.4 weeks), was studied with MR imaging first at a median postconceptional age of 31.9 weeks (range, 27.6 –38.1 weeks) and again at a median postconceptional age of 36.5 weeks (range, 33.4–42.9 weeks). The first MR imaging session was performed as soon as the infants were stable enough to be transported to the MR imaging unit; the second MR imaging session was performed at term-equivalent age or just before discharge or transfer from the hospital. Each of the neonates was studied with ultrasonography of the head according to the clinical protocol of our intensive care nursery. For all except three of the neonates, this included at least one session of ultrasonography of the head performed during the first 3 days of life, then weekly ultrasonography sessions until 3 weeks of life, and one ultrasonography session before discharge at or near term-equivalent age. One neonate underwent the first ultrasonography session on the eighth day of life and then underwent weekly follow-up studies. Two neonates in the cohort each underwent only a single ultrasonography session coincident with MR imaging that had normal findings on the eighth day of life and the 32nd day of life, respectively; considering the normal MR imaging results, follow-up ultrasonography was not performed.

Cranial Ultrasonography

Cranial ultrasonography was performed according to a clinical protocol, acquiring images in the sagittal, parasagittal, and coronal planes via the anterior fontanel by using a multifrequency (5–8 MHz) transducer. A midline sagittal view image and five to 10 parasagittal planes of the white matter of the corticospinal tracts were obtained on each side. Ten to 20 images, including the area of the frontal horns through the posterior periventricular white matter, were obtained in coronal planes. Two or three axial view images, including the regions of the cerebellum, fourth ventricle, and cisterna magna, were obtained via the posterior fontanel. All ultrasonograms were reviewed initially by a clinical ultrasonologist and subsequently by a single ultrasonologist who was blinded to the neonate’s clinical course, MR imaging findings, and findings of the clinical ultrasonologist. The sonographic images were reviewed for the diagnosis of intraventricular hemorrhage, ventricular enlargement, and white matter injury (14). Intraventricular hemorrhage was graded according to the system presented by Papile et al (15). Neonates were diagnosed with ventriculomegaly if the largest atrial ventricular diameter (obtained at the level of the glomus of the choroids plexus) measured >10 mm. A ventricular size of 8 to 10 mm was considered borderline. A grading system of white matter abnormalities was developed for both MR imaging and ultrasonography to determine whether even subtle ultrasonographic findings (those that might not be considered abnormal in general practice) might correlate with subtle MR imaging findings (Table 1). A score was developed to correspond to those abnormalities diagnosed by a clinical ultrasonologist, such that grades 0 to 1 would be diagnosed as normal, grades 2 to 4 would be diagnosed as abnormal periventricular echogenicity, and grade 5 would be diagnosed as macrocystic periventricular lesions. To determine the reliability of this score, the diagnosis of white matter abnormalities in the primary interpretation in the clinical record was compared with the interpretation of the ultrasonologist reviewing these cases for this study. For the diagnosis of abnormal periventricular echogenicity and periventricular cysts, the clinical and study ultrasonologists agreed in 87.5% of cases (κ=0.68, P < .00001). Abnormal periventricular echogenicity was defined as transient if the abnormal echogenicity was present for <7 days, persistent if the abnormal echogenicity was present for ≥7 days, and uncertain if a follow-up examination was not performed within 7 days of the study with abnormal findings. Both the highest grade of periventricular echogenicity and the grade of periventricular echogenicity on the last neonatal sonogram by the study ultrasonologist were used in the analysis.

View this table:

TABLE 1:

Grading of white matter abnormalities based on ultrasonography and MR imaging

MR Imaging

The premature neonates were studied longitudinally. The first MR imaging session was performed as soon after birth as the neonate was stable enough to be transported safely to the MR imaging unit and imaging time was available, and the second MR imaging session was performed just before discharge or transfer from the hospital. Twenty-three neonates did not require mechanical ventilatory support, were fed before the MR imaging examination, and needed no pharmacologic sedation. Five neonates required sedation with IV administered Nembutal for both studies. Four neonates required sedation for only one MR imaging session. All studies were performed by using a 1.5-T Signa EchoSpeed system (GE Medical Systems) with an MR-compatible isolette that was developed for these studies. A neonatologist in the MR imaging suite monitored the neonates during imaging and hand-ventilated the intubated neonates. The same MR imaging techniques were used for the entire cohort. MR images of the brain included the following for all neonates: 1) T1-weighted sagittal and axial view spin-echo images; 500/11/1 (TR/TE/number of excitations); section thickness, 4 mm; flip angle, 90 degrees; acquisition matrix, 192 × 256; 2) T2-weighted spin-echo images; 3000/60, 120; section thickness, 4 mm; flip angle, 90 degrees; acquisition matrix, 192 × 256; 3) coronal view spoiled gradient recall images; 36/2 (TR/number of excitations); partition size, 1.5 mm; TE=9 ms; flip angle, 35 degrees; field of view, 18 cm.

Two pediatric neuroradiologists interpreted each of the MR imaging studies blinded to the patients’ clinical conditions and ultrasonographic findings. Discrepancies were resolved by discussion and consensus.

The white matter abnormalities detected included foci of abnormal T1 hyperintensity in the absence of marked T2 hypointensity in the periventricular white matter and foci of low intensity on T1-weighted images. The constellation of T1 hyperintensity, in the absence of marked T2 hypointensity, most likely represented areas of gliosis, which have been seen pathologically in similar patient populations in other pathologic studies, whereas areas of low intensity on T1-weighted images likely represented cavitation (11, 16). Areas of T1 hyperintensity and significant T2 hypointensity (“blooming” on the 120 TE images more than on the 60 TE images) were interpreted as foci of hemorrhage. Based on the severity of white matter abnormalities shown by MR imaging, neonates were classified as having normal, minimal, moderate, or severe white matter abnormalities (Table 1). In developing this grading system of white matter abnormalities, two pediatric neuroradiologists independently interpreted 38 MR imaging studies blinded to the patients’ clinical conditions and achieved agreement in 89.5% of cases (κ=0.84, P < .00001).

Neonates were diagnosed with ventriculomegaly if the largest atrial ventricular diameter (at the level of the glomus of the choroid plexus) measured >10 mm and were diagnosed as borderline if it measured 8 to 10 mm. Intraventricular hemorrhage was graded by using the same scale as that used for the ultrasonography. The presence of other brain abnormalities was noted separately.

Statistical Analysis

Statistical analysis was conducted by using Stata (Stata Corporation, College Station, TX). Clinical variables were compared between the groups with and without white matter injury by using the Kruskal Wallis test or the Fisher exact test for categorical variables. The severity of white matter abnormalities shown by MR imaging was correlated with the severity of white matter abnormalities shown by ultrasonography by using the Spearman Rank Correlation for categorical data. The relative risk associated with white matter abnormalities shown by MR imaging was determined for the presence of abnormal periventricular echogenicity. To determine the clinical value of abnormal periventricular echogenicity on ultrasonograms as a predictor of white matter abnormalities shown by MR imaging, the sensitivity, specificity, and predictive values were calculated. The analyses considering the severity of abnormal periventricular echogenicity were repeated for both the highest grade of periventricular echogenicity and the grade of periventricular echogenicity on the last neonatal ultrasonogram. Because these statistical analyses compared the diagnosis of white matter abnormalities shown by MR imaging and ultrasonography within an individual neonate, potential confounding variables, such as the severity of intraventricular hemorrhage, were accounted for in these univariate analyses.

Results

White Matter Abnormalities

White matter abnormalities were diagnosed in 18 (56%) of the 32 neonates based on MR imaging; they were minimal in 10, moderate in seven, and severe in one (Figs 1 and 2). Because only one neonate had severe white matter abnormalities, this patient was included with the moderate group (all P > .1). The timing of the MR imaging and ultrasonography studies did not significantly differ across the groups. Male neonates were significantly more likely to have white matter abnormalities shown by MR imaging (P = .02). In other respects, the clinical characteristics of the groups with and without white matter abnormalities did not differ meaningfully (Table 2).

Fig 1.

Minimal white matter injury shown on ultrasonograms and MR images of premature neonate born 31.1 weeks after conception and studied at 32.9 weeks postconceptional age.

A, Coronal view transfontanel ultrasonograms show diffuse foci of mildly increased echogenicity (less than that of the choroid plexus) in addition to irregularity of the lateral borders of the periventricular white matter (arrowheads).

B, Corresponding MR images (spoiled gradient-echo volumetric images) show a few small foci of T1 hyperintensity in the absence of marked T2 hypointensity, which were thought to represent astrogliosis in the periventricular white matter without cavitation (arrow). The abnormalities shown by MR imaging and ultrasonography are not anatomically concordant, although both were graded as minimal white matter abnormalities.

Fig 2.

Images show moderate to severe white matter injury in a premature neonate born 29.1 weeks after conception and studied at 32 weeks postconceptional age

A, Coronal view transfontanel ultrasonogram shows small areas of hypoechogenicity in the periventricular white matter, indicating small areas of cavitation, in addition to pronounced ventriculomegaly (arrowhead).

B and C, Corresponding MR images (spoiled gradient-echo volumetric images) show small areas of T1 hypointensity, indicating cavitation in the periventricular white matter (B, arrow), in addition to multiple small foci of T1 hyperintensity in the absence of marked T2 hypointensity, which were thought to represent astrogliosis in the periventricular white matter (C, arrow). The degree of ventriculomegaly is similar on the ultrasonogram and MR images. Note that the areas of T1 hyperintensity are more extensive than the small cystic lesions evident on the ultrasonogram or MR images.

View this table:

TABLE 2:

Clinical characteristics of the MR imaging defined white matter abnormality groups

The most common white matter abnormalities observed were foci of T1 hyperintensity that were seen throughout the white matter, more commonly within 1 to 2 cm of the ventricles. These foci of T1 hyperintensity were occasionally associated with small areas (<2 mm) of T1 hypointensity, which were interpreted as cavitation. Of note, both the cavitary and noncavitary areas were detected better on the T1-weighted images than on the T2-weighted images. The white matter abnormalities were present on the first MR images of all neonates and remained unchanged on the second MR images, except for one neonate who had minimal abnormalities shown by the first MR imaging session and moderate abnormalities shown by the second; this neonate was classified as having moderate abnormalities. In this one neonate, white matter abnormalities progressed from minimal to moderate severity; in the other cases, however, the T1 hyperintensity became less conspicuous over time. Large cystic lesions were not observed in this cohort. Areas of white matter T1 hyperintensity and T2 hypointensity consistent with foci of hemorrhage were not observed.

Abnormal periventricular echogenicities were commonly observed on the ultrasonograms of all three MR imaging-classified groups and were present for 22 (69%) of the 32 neonates (Table 3). However, five neonates with moderate white matter abnormalities shown by MR imaging (62% of the moderate group) did not have significant periventricular echogenicity on the ultrasonograms. The single neonate with periventricular cysts (grade 5) shown by ultrasonography had severe white matter abnormalities shown by MR imaging with extensive foci of T1 hyperintensity, small areas of white matter cavitation (T1 hypointensity), and marked volume loss of white matter. The duration of the abnormal periventricular sonographic echodensity among the patients in the three MR imaging-defined groups was similar. The severity of white matter abnormalities shown by MR imaging was not correlated with the greater severity of white matter abnormalities detected with ultrasonography (rho=0.18, P=.3) or with the severity of white matter abnormalities on the last ultrasonograms (rho=0.16, P=.4).

View this table:

TABLE 3:

Highest grade of periventricular echogenicity and the grade of periventricular echogenicity shown on the last neonatal sonogram in the MR imaging-defined white matter abnormality groups

Intraventricular Hemorrhage and Ventriculomegaly

The diagnoses of intraventricular hemorrhage and ventriculomegaly were similar based on ultrasonography and MR imaging (Table 4). Of neonates with moderate white matter abnormalities, only four (50%) had associated ventriculomegaly; this was associated with grade 3 intraventricular hemorrhage in three.

View this table:

TABLE 4:

Highest grade of intraventricular hemorrhage, ventriculomegaly, and thalamic echogenicity in the MR imaging-defined white matter abnormality groups

Other Injury

One neonate had thalamostriate vasculopathy (branching curvilinear hyperechogenicity in the deep gray cerebral nuclei) shown by ultrasonography, although no thalamic or striatal abnormalities were evident based on MR imaging. Ultrasonographically abnormal thalamic echogenicity for two neonates and abnormal echogenicity in the tegmentum of the mesencephalon of another neonate did not correspond to thalamic or brain stem abnormalities shown by MR imaging.

Sonogram Predictors of MR Imaging-defined White Matter Abnormalities

The presence of significant periventricular echogenicity on ultrasonograms (grades 3–5) or definite ventriculomegaly had a high specificity and positive predictive value for white matter abnormalities shown by MR imaging (Table 5). These features, however, had a low sensitivity and only moderate negative predictive values for predicting minimal or moderate white matter abnormalities based on MR imaging.

View this table:

TABLE 5:

Periventricular echogenicity and ventriculomegaly shown on sonograms as predictors of MR imaging-defined white matter abnormalities^*

Discussion

Spectrum of White Matter Injury

We found cystic periventricular leukomalacia based on ultrasonograms for only one (3%) neonate. Although the presence of cystic periventricular changes shown by ultrasonography is specific for the diagnosis of periventricular leukomalacia (10) and correlates well with the development of motor and visual disabilities of affected children (1, 3–7, 17, 18), this type of lesion was distinctly uncommon in our cohort. Instead, we found scattered foci of predominantly noncavitary white matter abnormalities. The MR imaging characteristics of these lesions, with T1 hyperintensity in the absence of T2 hypointensity, are most consistent with increased focal cellularity secondary to astrogliosis, as shown by previous pathologic studies (11, 15). Such subtle white matter abnormalities have been associated with widespread impairment of cerebral development (19). Specifically, one study that used diffusion tensor imaging revealed that although anisotropy increased with age in all white matter regions in normal participants, it did not increase in frontal white matter in those with minimal white matter injury and in widespread white matter areas in those with moderate white matter injury (19). Another study that used volumetric MR imaging techniques showed that neonates with white matter abnormalities revealed by MR imaging, including those with diffuse rather than cystic abnormalities, had significantly lower volumes of cortical gray matter and myelinated white matter at term compared with control term infants (20). These results indicate that non-cystic white matter injury is associated with widespread impairments in cerebral development. Furthermore, the white matter abnormalities evident in our cohort present early in life and persist through the neonatal period. Therefore, this mild spectrum of white matter abnormalities detected only by MR imaging likely reflects an early and persistent form of white matter injury.

The finding that cystic periventricular leukomalacia is distinctly uncommon is consistent with other descriptions of MR imaging findings in recent cohorts of premature neonates (13, 21). Our findings, however, contrast with these other descriptions of white matter injury in that we did not observe hemorrhagic lesions or abnormal diffuse excessive high T2 signal intensity in the periventricular white matter (10, 13, 21). Several potential reasons might explain these discrepancies. In contrast with our cohort studied by using a 1.5-T MR imaging unit, other groups have studied premature neonates by using a 1.0-T unit. Other groups have selected neonates with abnormalities shown by sonography (10, 13, 21), whereas we recruited all neonates without brain anomalies, congenital infections, or catastrophic hemorrhages. Despite the discrepancies, these studies all indicated that MR imaging is a sensitive technique with which to detect white matter injury in premature neonates early in life.

Correspondence of Ultrasonography and MR Imaging for White Matter Abnormalities

Several groups have shown that macro-cystic lesions of the periventricular white matter (grade IV hemorrhage) in premature neonates, classic periventricular leukomalacia, and ventriculomegaly are associated with adverse neurodevelopmental outcomes (1, 3, 5, 6, 18, 22–24). In our cohort, these more severe sonographic abnormalities of the periventricular white matter were specific indicators of white matter abnormalities shown by MR imaging. Although the positive predictive value of these abnormalities shown by ultrasonography for predicting white matter abnormalities shown by MR imaging was high, the sensitivity of these findings was low. This is consistent with previous observations in which the correspondence between periventricular white matter abnormalities shown by sonography and MR imaging was best for neonates with cystic changes shown by sonography (8–10).

Because mild to moderate white matter injury may not cavitate, changes may not be detected by sonography of all premature neonates with periventricular white matter injury. This has been confirmed in some sonography-pathology correlation studies (6, 8, 25). Further, some cysts (<3 mm) may elude sonographic detection. This is consistent with the observation in this cohort that ultrasonography did not detect the small cavitations (<2 mm) observed with MR imaging in the periventricular white matter. These findings suggest that only periventricular cysts of sufficient size and severity are detected by sonography. In contrast with sonography, the extent and localization of MR imaging abnormalities in the white matter correspond closely to histopathologic changes found by postmortem examination (8, 11, 16, 25). However, in contrast to macro-cystic white matter injury, the neurodevelopmental consequences of the scattered foci of noncavitary or small cavitary abnormalities in the periventricular white matter are not yet defined.

No accepted in vivo measure of white matter injury in the premature neonate is currently available. Considering the strong association of MR imaging abnormalities in the white matter with injury evident on histopathology in other studies, we chose to compare the predictive value of white matter abnormalities shown by ultrasonography for those detected by MR imaging. In making this comparison, in the absence of an in vivo gold standard with which to compare both tests, the relatively poor sensitivity of ultrasonography for white matter abnormalities may have been exaggerated. However, the finding that sonography is relatively insensitive for the detection of mild white matter abnormalities detected by MR imaging is consistent with observations in other cohorts (8, 13, 21). Some investigators have reported that the duration of increased periventricular echogenicity, and not the degree of echogenicity, is the important predictive factor. It has been found that increased periventricular echogenicity persisting longer than 1 week significantly increases the risk of adverse outcome, whereas those lasting <1 week may be a normal finding (26, 27). Still others have suggested that rather than the duration of abnormal periventricular echogenicity, it is the timing of abnormal echogenicity after the first week of life or the degree of increased abnormal echogenicity that improves the predictive value of this finding for white matter injury shown by MR imaging (13, 27). In this cohort, no meaningful difference was observed in the duration of abnormal periventricular echogenicity on ultrasonograms among the MR imaging-defined white matter injury groups.

A limitation of this study was that all neonates in the cohort were not studied with ultrasonography and MR imaging on the same day. Although this would seem to limit our ability to compare these imaging techniques, the timing of the most severe abnormalities shown by ultrasonography was variable, with a marked tendency for ultrasonographically detected white matter abnormalities to resolve. This is an inherent problem in the diagnosis of white matter injury with ultrasonography and is in contrast to MR imaging, with which abnormalities in the white matter are stable over a period of weeks to several months. Therefore, calculating the predictive value of ultrasonography findings for MR imaging findings by using the most severe grade of echogenicity shown on the ultrasonograms would have biased our findings toward exaggerating the sensitivity of the ultrasonography. Because ultrsonography had limited sensitivity and high specificity for diagnosing MR imaging-detectable white matter injury, it is unlikely that the timing of the ultrasonograms studied in relation to the MR images substantially biased the comparison of the most severe abnormalities shown by ultrasonography with the MR imaging findings. Furthermore, consistent with previous observations, neither the periventricular echogenicities shown on the ultrasonograms nor the white matter injury detected by MR imaging progressed to macro-cystic periventricular white matter injury or classic periventricular leukomalacia (27).

The impact of the white matter lesions detected by MR imaging on neurodevelopmental outcome needs to be determined to understand the true importance of these MR imaging findings. Neurodevelopmental outcome after neonatal brain injury likely reflects both the severity of the brain injury measured by neuroimaging in addition to other genetic and environmental factors such as socioeconomic status (5, 28). However, because a substantial number of premature neonates with abnormal neurodevelopmental outcomes have normal ultrasonography findings during the neonatal period (23, 29), it will be important to determine whether these neonates have MR imaging-detectable white matter injury.

Other Lesions

Unlike the findings in the cerebral white matter, ultrasonography and MR imaging corresponded well regarding intraventricular hemorrhage and ventriculomegaly. Although ventriculomegaly was a highly specific sign for moderate white matter injury (and, when present, had a high predictive value), it was not a sensitive sign.

Conclusion

This study supports the previous observations that cystic periventricular leukomalacia is becoming distinctly uncommon (13, 21). Instead, the premature neonates in this study commonly had scattered foci of abnormalities in the periventricular white matter. This white matter injury was detected early in life by using MR imaging and persisted through the neonatal period. Although ultrasonography offers many advantages for screening premature neonates for white matter injury (noninvasive, inexpensive, and portable), it was not a sensitive predictor of the milder spectrum of MR imaging-defined white matter abnormalities. Better MR imaging techniques (such as diffusion-tensor MR imaging) and proton MR spectroscopy may offer the potential for even earlier diagnosis of this form of brain injury (30, 31). The neurodevelopmental consequences of the milder spectrum of white matter injury detected by MR imaging are not yet known and are currently being prospectively determined.

Acknowledgments

The authors thank the neonatal nurses of the Pediatric Clinical Research Center for help in screening and transporting neonates to the MR imaging unit. The authors also thank Dr. Shannon Hamrick for critical comments on the manuscript.

Footnotes

Supported by the National Institutes of Health grant NS35902 and the National Institutes of Health Pediatric Clinical Research Center grants M01-RR01271 and RO1 NS40117. S.P.M. is supported by the Canadian Institutes of Health Research Clinician Scientist Program (Phase I).

References

↵
Fawer CL, Diebold P, Calame A. Periventricular leucomalacia and neurodevelopmental outcome in preterm infants. Arch Dis Child 1987;62:30–36
Abstract/FREE Full Text
Hack M, Fanaroff AA. Outcomes of children of extremely low birthweight and gestational age in the 1990’s. Early Hum Dev 1999;53:193–218
CrossRef PubMed
↵
Vohr BR, Wright LL, Dusick AM, et al. Neurodevelopmental and functional outcomes of extremely low birth weight infants in the National Institute of Child Health and Human Development Neonatal Research Network, 1993–1994. Pediatrics 2000;105:1216–1226
Abstract/FREE Full Text
Cioni G, Fazzi B, Coluccini M, Bartalena L, Boldrini A, van Hof-van Duin J. Cerebral visual impairment in preterm infants with periventricular leukomalacia. Pediatr Neurol 1997;17:331–338
CrossRef PubMed
↵
Piecuch RE, Leonard CH, Cooper BA, Sehring SA. Outcome of extremely low birth weight infants (500 to 999 grams) over a 12-year period. Pediatrics 1997;100:633–639
Abstract/FREE Full Text
↵
Volpe J. Neurology of the Newborn. 4th ed. Philadelphia: W.B. Saunders Company;2001
↵
Jacobson L, Ygge J, Flodmark O. Oculomotor findings in preterm children with periventricular leukomalacia: a connection between lesions in the periventricular area and eye motility disorders? Acta Ophthalmol Scand 1996;74:645
PubMed
↵
Childs AM, Cornette L, Ramenghi LA, et al. Magnetic resonance and cranial ultrasound characteristics of periventricular white matter abnormalities in newborn infants. Clin Radiol 2001;56:647–655
CrossRef PubMed
de Vries LS, Eken P, Groenendaal F, van Haastert IC, Meiners LC. Correlation between the degree of periventricular leukomalacia diagnosed using cranial ultrasound and MRI later in infancy in children with cerebral palsy. Neuropediatrics 1993;24:263–268
PubMed
↵
Sie LT, van der Knapp MS, van Wezel-Meijler G, Taets van Amerongen AH, Lafeber HN, Valk J. Early MR features of hypoxic-ischemic brain injury in neonates with periventricular densities on sonograms. AJNR Am J Neuroradiol 2000;21:852–861
Abstract/FREE Full Text
↵
Schouman-Claeys E, Henry-Feugeas MC, Roset F, et al. Periventricular leukomalacia: correlation between MR imaging and autopsy findings during the first 2 months of life. Radiology 1993;189:59–64
PubMed
Keeney SE, Adcock EW, McArdle CB. Prospective observations of 100 high-risk neonates by high-field (1.5 Tesla) magnetic resonance imaging of the central nervous system: II. lesions associated with hypoxic-ischemic encephalopathy. Pediatrics 1991;87:431–438
Abstract/FREE Full Text
↵
Maalouf EF, Duggan PJ, Counsell SJ, et al. Comparison of findings on cranial ultrasound and magnetic resonance imaging in preterm infants. Pediatrics 2001;107:719–727
Abstract/FREE Full Text
↵
Barkovich AJ. Pediatric Neuroimaging. 3rd ed. Philadelphia: Lippincott Williams & Wilkins;2000
↵
Papile LA, Burstein J, Burstein R, Koffler H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr 1978;92:529–534
CrossRef PubMed
↵
Felderhoff-Mueser U, Rutherford MA, Squier WV, et al. Relationship between MR imaging and histopathologic findings of the brain in extremely sick preterm infants. AJNR Am J Neuroradiol 1999;20:1349–1357
Abstract/FREE Full Text
↵
Eken P, de Vries LS, van Nieuwenhuizen O, Schalij-Delfos NE, Reits D, Spekreijse H. Early predictors of cerebral visual impairment in infants with cystic leukomalacia. Neuropediatrics 1996;27:16–25
PubMed
↵
van de Bor M, den Ouden L, Guit GL. Value of cranial ultrasound and magnetic resonance imaging in predicting neurodevelopmental outcome in preterm infants. Pediatrics 1992;90:196–199
Abstract/FREE Full Text
↵
Miller SP, Vigneron DB, Henry RG, et al. Serial quantitative diffusion tensor MRI of the premature brain: development in newborns with and without injury. J Magn Reson Imaging 2002;16:621–632
CrossRef PubMed
↵
Inder TE, Huppi PS, Warfield S, et al. Periventricular white matter injury in the premature infant is followed by reduced cerebral cortical gray matter volume at term. Ann Neurol 1999;46:755–760
CrossRef PubMed
↵
Maalouf EF, Duggan PJ, Rutherford MA, et al. Magnetic resonance imaging of the brain in a cohort of extremely preterm infants. J Pediatr 1999;135:351–357
CrossRef PubMed
↵
Ment LR, Vohr B, Allan W, et al. The etiology and outcome of cerebral ventriculomegaly at term in very low birth weight preterm infants. Pediatrics 1999;104:243–248
Abstract/FREE Full Text
↵
Roth SC, Baudin J, McCormick DC, et al. Relation between ultrasound appearance of the brain of very preterm infants and neurodevelopmental impairment at eight years. Dev Med Child Neurol 1993;35:755–768
PubMed
↵
Whitaker AH, Feldman JF, Van Rossem R, et al. Neonatal cranial ultrasound abnormalities in low birth weight infants: relation to cognitive outcomes at six years of age. Pediatrics 1996;98:719–729
Abstract/FREE Full Text
↵
Hope PL, Gould SJ, Howard S, Hamilton PA, Costello AM, Reynolds EO. Precision of ultrasound diagnosis of pathologically verified lesions in the brains of very preterm infants. Dev Med Child Neurol 1988;30:457–471
PubMed
↵
de Vries LS, Rademaker KJ, Groenendaal F, et al. Correlation between neonatal cranial ultrasound, MRI in infancy and neurodevelopmental outcome in infants with a large intraventricular haemorrhage with or without unilateral parenchymal involvement. Neuropediatrics 1998;29:180–188
PubMed
↵
van Wezel-Meijler G, van der Knaap MS, Sie LT, et al. Magnetic resonance imaging of the brain in premature infants during the neonatal period: normal phenomena and reflection of mild ultrasound abnormalities. Neuropediatrics 1998;29:89–96
PubMed
↵
Miller S, Newton N, Ferriero D, et al. Predictors of 30-month outcome after perinatal depression: role of proton MRS and socioeconomic factors. Pediatr Res 2002;52:71–77
PubMed
↵
Goldstein RB, Filly RA, Hecht S, Davis S. Noncystic “increased” periventricular echogenicity and other mild cranial sonographic abnormalities: predictors of outcome in low birth weight infants. J Clin Ultrasound 1989;17:553–562
PubMed
↵
Inder T, Huppi PS, Zientara GP, et al. Early detection of periventricular leukomalacia by diffusion-weighted magnetic resonance imaging techniques. J Pediatr 1999;134:631–634
CrossRef PubMed
↵
Vigneron DB, Barkovich AJ, Noworolski SM, et al. Three-dimensional proton MR spectroscopic imaging of premature and term neonates. AJNR Am J Neuroradiol 2001;22:1424–1433
Abstract/FREE Full Text

Received December 18, 2002.
Accepted after revision April 14, 2003.

View Abstract

[1] ↵
Fawer CL, Diebold P, Calame A. Periventricular leucomalacia and neurodevelopmental outcome in preterm infants. Arch Dis Child 1987;62:30–36
Abstract/FREE Full Text

[2] Hack M, Fanaroff AA. Outcomes of children of extremely low birthweight and gestational age in the 1990’s. Early Hum Dev 1999;53:193–218
CrossRef PubMed

[3] ↵
Vohr BR, Wright LL, Dusick AM, et al. Neurodevelopmental and functional outcomes of extremely low birth weight infants in the National Institute of Child Health and Human Development Neonatal Research Network, 1993–1994. Pediatrics 2000;105:1216–1226
Abstract/FREE Full Text

[4] Cioni G, Fazzi B, Coluccini M, Bartalena L, Boldrini A, van Hof-van Duin J. Cerebral visual impairment in preterm infants with periventricular leukomalacia. Pediatr Neurol 1997;17:331–338
CrossRef PubMed

[5] ↵
Piecuch RE, Leonard CH, Cooper BA, Sehring SA. Outcome of extremely low birth weight infants (500 to 999 grams) over a 12-year period. Pediatrics 1997;100:633–639
Abstract/FREE Full Text

[6] ↵
Volpe J. Neurology of the Newborn. 4th ed. Philadelphia: W.B. Saunders Company;2001

[7] ↵
Jacobson L, Ygge J, Flodmark O. Oculomotor findings in preterm children with periventricular leukomalacia: a connection between lesions in the periventricular area and eye motility disorders? Acta Ophthalmol Scand 1996;74:645
PubMed

[8] ↵
Childs AM, Cornette L, Ramenghi LA, et al. Magnetic resonance and cranial ultrasound characteristics of periventricular white matter abnormalities in newborn infants. Clin Radiol 2001;56:647–655
CrossRef PubMed

[9] de Vries LS, Eken P, Groenendaal F, van Haastert IC, Meiners LC. Correlation between the degree of periventricular leukomalacia diagnosed using cranial ultrasound and MRI later in infancy in children with cerebral palsy. Neuropediatrics 1993;24:263–268
PubMed

[10] ↵
Sie LT, van der Knapp MS, van Wezel-Meijler G, Taets van Amerongen AH, Lafeber HN, Valk J. Early MR features of hypoxic-ischemic brain injury in neonates with periventricular densities on sonograms. AJNR Am J Neuroradiol 2000;21:852–861
Abstract/FREE Full Text

[11] ↵
Schouman-Claeys E, Henry-Feugeas MC, Roset F, et al. Periventricular leukomalacia: correlation between MR imaging and autopsy findings during the first 2 months of life. Radiology 1993;189:59–64
PubMed

[12] Keeney SE, Adcock EW, McArdle CB. Prospective observations of 100 high-risk neonates by high-field (1.5 Tesla) magnetic resonance imaging of the central nervous system: II. lesions associated with hypoxic-ischemic encephalopathy. Pediatrics 1991;87:431–438
Abstract/FREE Full Text

[13] ↵
Maalouf EF, Duggan PJ, Counsell SJ, et al. Comparison of findings on cranial ultrasound and magnetic resonance imaging in preterm infants. Pediatrics 2001;107:719–727
Abstract/FREE Full Text

[14] ↵
Barkovich AJ. Pediatric Neuroimaging. 3rd ed. Philadelphia: Lippincott Williams & Wilkins;2000

[15] ↵
Papile LA, Burstein J, Burstein R, Koffler H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr 1978;92:529–534
CrossRef PubMed

[16] ↵
Felderhoff-Mueser U, Rutherford MA, Squier WV, et al. Relationship between MR imaging and histopathologic findings of the brain in extremely sick preterm infants. AJNR Am J Neuroradiol 1999;20:1349–1357
Abstract/FREE Full Text

[17] ↵
Eken P, de Vries LS, van Nieuwenhuizen O, Schalij-Delfos NE, Reits D, Spekreijse H. Early predictors of cerebral visual impairment in infants with cystic leukomalacia. Neuropediatrics 1996;27:16–25
PubMed

[18] ↵
van de Bor M, den Ouden L, Guit GL. Value of cranial ultrasound and magnetic resonance imaging in predicting neurodevelopmental outcome in preterm infants. Pediatrics 1992;90:196–199
Abstract/FREE Full Text

[19] ↵
Miller SP, Vigneron DB, Henry RG, et al. Serial quantitative diffusion tensor MRI of the premature brain: development in newborns with and without injury. J Magn Reson Imaging 2002;16:621–632
CrossRef PubMed

[20] ↵
Inder TE, Huppi PS, Warfield S, et al. Periventricular white matter injury in the premature infant is followed by reduced cerebral cortical gray matter volume at term. Ann Neurol 1999;46:755–760
CrossRef PubMed

[21] ↵
Maalouf EF, Duggan PJ, Rutherford MA, et al. Magnetic resonance imaging of the brain in a cohort of extremely preterm infants. J Pediatr 1999;135:351–357
CrossRef PubMed

[22] ↵
Ment LR, Vohr B, Allan W, et al. The etiology and outcome of cerebral ventriculomegaly at term in very low birth weight preterm infants. Pediatrics 1999;104:243–248
Abstract/FREE Full Text

[23] ↵
Roth SC, Baudin J, McCormick DC, et al. Relation between ultrasound appearance of the brain of very preterm infants and neurodevelopmental impairment at eight years. Dev Med Child Neurol 1993;35:755–768
PubMed

[24] ↵
Whitaker AH, Feldman JF, Van Rossem R, et al. Neonatal cranial ultrasound abnormalities in low birth weight infants: relation to cognitive outcomes at six years of age. Pediatrics 1996;98:719–729
Abstract/FREE Full Text

[25] ↵
Hope PL, Gould SJ, Howard S, Hamilton PA, Costello AM, Reynolds EO. Precision of ultrasound diagnosis of pathologically verified lesions in the brains of very preterm infants. Dev Med Child Neurol 1988;30:457–471
PubMed

[26] ↵
de Vries LS, Rademaker KJ, Groenendaal F, et al. Correlation between neonatal cranial ultrasound, MRI in infancy and neurodevelopmental outcome in infants with a large intraventricular haemorrhage with or without unilateral parenchymal involvement. Neuropediatrics 1998;29:180–188
PubMed

[27] ↵
van Wezel-Meijler G, van der Knaap MS, Sie LT, et al. Magnetic resonance imaging of the brain in premature infants during the neonatal period: normal phenomena and reflection of mild ultrasound abnormalities. Neuropediatrics 1998;29:89–96
PubMed

[28] ↵
Miller S, Newton N, Ferriero D, et al. Predictors of 30-month outcome after perinatal depression: role of proton MRS and socioeconomic factors. Pediatr Res 2002;52:71–77
PubMed

[29] ↵
Goldstein RB, Filly RA, Hecht S, Davis S. Noncystic “increased” periventricular echogenicity and other mild cranial sonographic abnormalities: predictors of outcome in low birth weight infants. J Clin Ultrasound 1989;17:553–562
PubMed

[30] ↵
Inder T, Huppi PS, Zientara GP, et al. Early detection of periventricular leukomalacia by diffusion-weighted magnetic resonance imaging techniques. J Pediatr 1999;134:631–634
CrossRef PubMed

[31] ↵
Vigneron DB, Barkovich AJ, Noworolski SM, et al. Three-dimensional proton MR spectroscopic imaging of premature and term neonates. AJNR Am J Neuroradiol 2001;22:1424–1433
Abstract/FREE Full Text

Main menu

User menu

Search

American Journal of Neuroradiology

Comparing the Diagnosis of White Matter Injury in Premature Newborns with Serial MR Imaging and Transfontanel Ultrasonography Findings

Abstract