ABSTRACT
One of two late preterm twins at gestational age 36 weeks suffered idiopathic cerebral infarction. The first symptom was an apneic attack about 3 hours after birth. The lesion was extensive in the left middle cerebral artery region. Cord blood and early postnatal serum levels of high mobility group box-1 (HMGB-1), histoneH3, and syndecan-1 were measured simultaneously. All values of HMGB-1 remained within the reference value range. HMGB-1 and histoneH3 showed a very strong positive correlation (r=0.956). Syndecan-1 was detected but did not show a significant correlation with either HMGB-1 or histoneH3. This twin was delivered by Caesarean section before the first labor pains, and it was suspected that the ischemia-reperfusion injury that occurs at birth was minimal. Based on the serial changes of HMGB-1 in the early postnatal period, including in the umbilical cord blood, it is highly possible that the cerebral infarction had already occurred before birth. This case suggests that measurement of these three biomarkers released into the blood by ischemic reperfusion injuries such as stroke may be also useful for predicting these onsets.
Keywords: high mobility group box-1; histoneH3; ischemia-reperfusion injury; neonatal stroke; syndecan-1
Introduction
Neonatal cerebral infarction is a relatively rare central nervous
system disorder that occurs in about 1 in 5000 neonates. The most
common cause is ischemic cerebral injury resulting from neonatal
asphyxia but can also be idiopathic. Half of the infarctions develop
by the day 1, and few occur over the 3rd day of life. Most occur in
the middle cerebral artery region, most often on the left side [1-
3]. Convulsions are the most common initial symptom, but there
are many non-specific symptoms such as decreased feeding ability
and apneic attacks. Treatment is mainly systemic management
and symptomatic treatment for convulsions. Currently, there are
only a few reported cases of the use of thrombomodulin, tissue
plasminogen activator, and Edaravone® (free radical scavenger),
of which treatment method has been useful in adults [4], probably
because of the many side effects for neonates. Neonatal cerebral
infarction is currently classified into six categories from the
viewpoint of pathogenesis, and most of the idiopathic cerebral
infarctions belong to the category of ischemic cerebral infarction
[1,2]. Similar cerebral ischemia and subsequent inflammation are
pathological conditions of cerebral infarction in both newborns
and adults, and the indication for treatment depends on how
many hours have passed since the onset of cerebral infarction. In
newborns, infarct lesions may appear shortly after birth or may
have already occurred before birth and may be diagnosed by the
detection of postnatal symptomsin the infant. Therefore, it is very
difficult to determine the onset of neonatal cerebral infarction
compared to that of adults.
We have confirmed and reported in a multicenter cohort study
that the effectiveness of brain hypothermia in neonatal asphyxia
can be judged by changes in the serum high mobility group box-
1 (HMGB-1) concentration [5]. Furthermore, we observed the
serial changes of HMGB-1 in the blood of infants who had already
developed fetal asphyxia and suffered severe sequelae even though
brain hypothermia was started within 6 hours after birth. We found
that a long time had passed following the onset of ischemic lesions
and reported that postnatal brain hypothermia may be ineffective
for such hypoxic ischemic encephalopathy within utero onset [6].
This time we experienced a case of cerebral infarction in one of two
twins. We had the opportunity to simultaneously measure three
biomarkers, HMGB-1, histone H3, which is a nuclear protein similar
to HMGB-1, and syndecan-1, which is present on the surface of
vascular endothelial cells and is thought to be released in the blood
during angiopathy. As a result, we report a case in which the onset
of cerebral infarction was suspected to have occurred before birth.
Case Presentation
The mother was 35 years old and had one pregnancy and zero deliveries. She had preeclampsia and was indicated for an emergency caesarean section due to exacerbation of her hypertension on the 36th week, 3rd day of her pregnancy. A female with a birth weight of 2420 g was born as the second baby of a diamniotic dichorionic twin pregnancy with an Apgar score of 8-9 and umbilical arterial pH of 7.273. At 2 hours and 54 minutes after her birth, she was admitted to the NICU due to an apneic attack. The infant was given intravenous phenobarbital for pedaling-like and muffled mouth movements on day 1 after birth, but it was ineffective and was changed to continuous administration of midazolam on day 2. Head echo showed no obvious lesions, but computed tomography and magnetic resonance imaging showed extensive cerebral infarction in the left middle cerebral artery region (Figure 1). The patient was diagnosed as having idiopathic cerebral infarction because a coagulation system test, amino acid fraction, and ophthalmologic examination were all negative. Midazolam was used from 2 to 8 days of age. No particular abnormalities such as in oral feeding and muscle tone were observed. An electroencephalogram was performed on day 22, and a decrease in activity on the left side was observed, but no obvious seizures were observed, so the patient was discharged from the hospital on day 31 after birth.
Material and Methods
Measurement of HMGB-1 Levels
The HMGB-1 measurements were performed by technicians with no knowledge of the personal data of the patient providing the samples using a commercially available ELISA kit (Shino-Test Corporation, Sagamihara, Japan). The detection sensitivity of this assay system was 0.2 ng/mL [7].
Measurement of HistoneH3 Levels
Because there is no commercially available ELISA kit, the measurement of histone H3 was performed by the ELISA prepared in our laboratory. The following is the method which had been presented in our laboratory was adopted this time as well [8]. Polystyrene microtiter plates (Nunc, Roskilde, Denmark) were coated with 100μL/well of 1 mg/L anti-histone H3 peptide polyclonal antibody (Shino-Test Corporation) in phosphatebuffered saline (PBS), and incubated overnight at 2–8°C. After three washes with PBS containing 0.05% Tween-20 (washing buffer), the remaining binding sites were blocked by incubation with 400 μL/well of PBS containing 1% bovine serum albumin (BSA) for 2 h. The plates were washed again and incubated with 100 μL/ well of diluted calibrator and serum samples (1:10 dilution in 0.2 mol/L Tris pH 8.5, 0.15 mol/L NaCl, and 1% BSA) for 24 h at room temperature. After washing, the plates were incubated with 100 μL/ well of anti-histoneH3 peroxidase-conjugated peptide polyclonal antibody (Shino-Test Corporation) for 2 hours at room temperature. The plates were washed again, and the chromogenic substrate 3,3′,5,5′-tetra-methylbenzidine (TMBZ; Dojindo Laboratories, Kumamoto, Japan) was added to each well. The reaction was terminated with 0.35 mol/L Na2SO4, and the absorbance at 450 nm was measured with a microplate reader (Model 680; Bio-Rad, Hercules, CA, USA). A standard curve was obtained with purified calf thymus histoneH3 (Roche, Stockholm, Sweden). The amino acid sequence of histone H3 is highly conserved throughout species, and that of the antibody recognition in humans, calves, mice, and rats. This ELISA specifically detects histone H3 and does not react with other histone family proteins, including histone H2A, H2B, and H4, even if 104 times excess proteins are loaded. The detection sensitivity of this assay system was 2.0 ng/mL.
Measurement of Syndecan-1 Levels
The following is the ELISA method which was presented originally in our laboratory. Polystyrene microtiter plates (Nunc, Roskilde, Denmark) were coated with 100 μL anti-syndecan-1 monoclonal antibody (R&D Systems) in PBS, and the plates were sealed with a thin adhesive-coated plastic sheet and incubated overnight at 37°C. The unbound antibodies were removed by washing the plate 3 times with PBS containing 0.05% Tween 20, and the remaining binding sites in the wells were blocked by incubating the plates for 2 h with 400 μL/well of PBS containing 1% BSA. After washing, 100 μL of each dilution of the standard and samples in 0.2 mol/L Tris pH 7.4 and 0.15 mol/L NaCl2 containing 1% BSA was added to the wells. The samples and recombinant syndecan-1 standard were diluted 1:10. The microtiter plates were incubated for 20–24 hours at room temperature. After washing, 100 μL per well of anti-human syndecan-1 peroxidase-conjugated polyclonal antibody (R&D Systems) was added, and the plates were incubated at room temperature for 2 h. After washing, TMBZ (Dojindo Laboratories, Kumamoto, Japan) was added to each well. The enzyme reaction was allowed to proceed for 30 min at room temperature. The chromogenic substrate reaction was stopped by addition of stop solution (0.35 mol/L Na2SO4), and the absorbance was read at 450 nm.
Ethical Approval
This study was approved by the ethics committees of the Japanese Red Cross Musashino Hospital (#28060). Parents of the twins were informed of the study design, and their written informed consent was obtained
Results
HMGB-1 and histone H3, which are common substances as nuclear proteins, showed a fairly strong positive correlation with a correlation coefficient of r = 0.965 (Figure 2). Syndecan-1 was low in both twins at each measurement, and no significant correlation was observed between HMGB-1 and histone H3 as previously reported [14]. HMGB-1 and histone H3 showed no significant variation in their levels in the specimens obtained before and after the onset of the first apneic attack (Figure 3).
Discussion
Treatment for ischemic lesions of the brain is more effective
the sooner it can be initiated after ischemia onset. Within 6 hours
after the onset of ischemic lesions, HMGB-1 released from injured
cells disrupts the blood-brain barrier (BBB) [9]. Then, within 24
hours after lesion onset, peroxiredoxin released from the cells
acts on macrophages migrating from the injured part of the BBB
to release inflammatory cytokines such as IL-1β and TNFα. Then,
24 hours after the onset, IL-17 and IFNγ are released from T
cells, exacerbating damage to the BBB and brain cells [4,10]. The
indication for brain hypothermia to treat neonatal hypoxic-ischemic
encephalopathy is “the treatment can be started within 6 hours
after birth”, and that for Edaravone®, a free radical scavenger, as a
treatment for cerebral infarction in adults is “the treatment should
start within 72 hours of onset”. These indications make sense
in terms of protecting against this inflammatory response after
temporal ischemia. In adults, the origin of onset is often clear, but
in newborns, onset does not always occur at birth. In our previous
case, severe ischemic encephalopathy had already occurred before
birth, and the ischemic encephalopathy became severe even though
brain hypothermia was performed within 6 hours after birth [6].
The serum cytokine profile and HMGB-1 level in this case was
measured over time to develop a theoretical diagnosis and report.
We consider that asphyxia is a condition of systemic ischemiareperfusion
and cerebral infarction is a condition of local ischemiareperfusion.
Both HMGB-1 and histoneH3 are nuclear proteins. It was
expected that the blood concentrations of these two substances
would correlate, as they would be released into the blood when
the cells were injured. Although the number of samples obtained
was small, the values showed a very strong positive correlation (r =
0.965). In contrast, the serum HMGB-1 levels in this twin remained
within reference values we have already reported for all cord blood
and early postnatal specimens [7]. HistoneH3, which showed a
strong correlation, was also about the same value. As this baby was
born by a caesarean section before labor, it was inferred that the
so-called “physiological ischemia-reperfusion stress” associated
with birth would be minimal [11]. In addition, the changes in the
HMGB-1 level suggested that the probability of developing cerebral
infarction from immediately after birth to the onset of the apnea was
extremely low. Considering that the apneic attack occurred early
after birth, it is highly possible that the onset of cerebral infarction
in this baby occurred prenatally and that most of the injury process
was already completed by the time of birth. This suggested a reason
why the HMGB-1 and histoneH3 levels in the cord blood at birth
and as measured after birth did not increase [12,13].
Syndecan-1 is a representative proteoglycan expressed
on the surface of vascular endothelial cells. So far, it has been
reported that syndecan-1 is released into the bloodstream due to
vascular endothelial cell damage in the early stage of sepsis [14].
Furthermore, it has been confirmed to increase in an ischemic
perfusion injury model used in the animal experiment of Gayosso et
al. [15]. Syndecan-1 did not significantly correlate with HMGB-1 and
histone H3. This result was consistent with the report in adults by
Ikeda et al. To the best of our knowledge, the Ikeda et al. [14] report,
which focused on sepsis rather than cerebral infarction, is the only
report of the simultaneous measurement of the three biomarkers
HMGB-1, histone H3, and syndecan-1. The presentcase may be the
second report and especially the first report in newborns. When
released extracellularly, HMGB-1 not only directly damages the
BBB but also acts on monocytes to increase the expression level of
tissue factor and promote fibrin production by thrombin, thereby
promoting thrombus formation [4]. Histone H3, a structure of NETs
(neutrophil extracellular traps) released from neutrophils, is also
involved in thrombus formation when released extracellularly [8].
Furthermore, syndecan-1 is also exfoliated and released into the
bloodstream when vascular endothelial cells are damaged, and
a thrombus is formed on the surface of the vascular endothelial
cells [14]. If it can be confirmed that the levels of these three
substances, which are released in common into the blood stream
due to cells damaged by ischemia-reperfusion injury, are elevated
in the acute phase, the use of drugs such as thrombomodulin and
Edaravone® may be effective for neonatal cerebral infarction. Future
accumulation of additional cases and simultaneous measurement
of these three biomarkers must be useful for determining the onset
of cerebral infarction.
Conflict of Interest Statement
The authors have no conflicts of interest to declare.
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