Introduction

Hypertensive diseases of pregnancy are classified as preeclampsia–eclampsia, chronic hypertension, preeclampsia–eclampsia developed in the background of chronic hypertension, and transient hypertension [19]. The uteroplacental unit is one of the organs which is affected by capillary damage in hypertensive pregnant women. Early and long-term hypertension may lead to uteroplacental failure, fetal distress, intrauterine growth retardation (IUGR) and preterm delivery. It was shown that the risk of polycythemia was higher in babies of hypertensive mothers compared to the general population and maternal hypertension constituted a significant risk for polycythemia independent of fetal growth [12]. It has been reported that nucleated red blood cells increase secondary to uteroplacental hypoperfusion in babies of preeclamptic mothers [17]. In addition, it was shown that the possibility of thrombocytopenia was higher in newborns of preeclamptic mothers who had hypertension and especially thrombocytopenia, compared to normotensive mothers [4, 16]. Preeclampsia has been reported to be a risk factor for neonatal neutropenia and infections in premature newborns [6]. Therefore, early detection and prophylactic treatment are recommended in newborns at high risk.

Newborns of hypertensive mothers have a risk for polycythemic, infectious, and bleeding complications. However, there is no study comprehensively investigating the changes in hematologic parameters in the newborns which may be caused by hypertension in the mothers. In this study, the changes in the hematologic parameters were investigated in newborns of hypertensive mothers, including the morphologies of blood cells.

Materials and methods

Thirty-one pregnant women with a diagnosis of hypertension for at least 3 months and their newborns constituted the study group, and 32 healthy pregnant women and their newborns constituted the control group. Arterial blood pressure ≥140/90 mmHg was defined as hypertension. Women who have hypertension with proteinuria and/or edema that happens after 20th gestational week were defined as preeclamptic pregnant women. Women who have hypertension without the other signs of preeclampsia that happens during the pregnancy were defined as pregnant women with transient hypertension. Women who had hypertension also before the pregnancy or whose blood pressure ≥140/90 mmHg before the 20th gestational week were defined as chronic hypertensive pregnant women [19]. Newborns whose mothers used another drug in addition to anti-hypertensive drugs, whose mothers had another chronic disease, whose gestational age was <24 weeks, who had chromosomal anomalies, congential metabolic diseases, congenital malformations, premature rupture of membranes, perinatal infections and hematologic or endocrine diseases were excluded from the study.

The demographic data of the mothers (age, chronic disease, drug usage, parity, blood group, gestational week, interventional procedures during pregnancy, problems during pregnancy, mode of delivery, administration of anesthesia, delivery induction, presence of meconium, fetal deceleration and presence of a nuchal cord), birth weight of the newborn, gender of the newborn, Apgar scores at the first and fifth minutes and resuscitation status were recorded. Before the investigations were initiated, the content of the study was explained to the families and written informed consent was obtained.

In all subjects, umbilical cord blood was obtained after delivery and complete blood count, peripheral blood smear, reticulocyte count, serum vitamin B12, folate, ferritin levels and hemoglobin electrophoresis analyses were performed. Complete blood count was performed by a hemocytometer after routine daily calibration (Beckman Coulter PN 72377817, 2004 Fullerton, California, USA). Serum vitamin B12 (reference range 200–835 pg/mL), folate (reference range 5-21 ng/mL) and ferritin levels (reference range 13–150 ng/mL) were measured using a Modular Analytics E170 device with electrochemiluminescence immunologic test system (Hitachi Automatic Analyzer 1679-01 Tokyo, Japan) and hemoglobin electrophoresis was performed using a Sebia Hydrasys device with a semi-automatic agaroze gel electrophoresis system (Model 3187, 02/49, France).

In peripheral blood smears, neutrophils were examined in terms of hypersegmentation, nuclear abnormalities (a nucleus with hook, lump, flag-like projections or microlobes and pseudo Pelger–Huet anomalies), cytoplasmic abnormalities (hypogranulation or agranulation and granule distribution abnormalities), and membrane abnormalities (protrusion, loss of integrity). A segmentation index was calculated ([number of neutrophils with ≥5 lobes/number of neutrophils with 4 lobes] × 100) and a value of >16.9 was considered to be abnormal [2]. Smears with 2 % or more damaged nuclei was considered a nuclear structural defect, smears with 2 % or more hypogranulation was considered agranulation, smears with granule distribution abnormalities were considered cytoplasmic granule defects and smears with loss of membrane integrity were considered membrane abnormalities. One hundred thrombocytes were examined to detect the presence of giant thrombocytes (>20 % of thrombocytes with a diameter of >4 μm and >3 % of thrombocytes with a diameter >8 μm). The detected erythrocyte anomalies (spherocytes, poikilocytosis, polychromasia, anisocytosis, etc.) were also recorded.

Statistical analysis

The data were analyzed and processed in the computer using SPSS for Windows 11.0 Package program. In descriptive statistics, numbers and percentages were used for discontinuous variables, mean ± standard deviation and minimum and maximum values were used for continuous variables. Chi-square (χ 2) was used for comparison of discontinuous variables. The differences between groups were compared using T tests for the ones with a normal distribution and Mann–Whitney tests for the ones which had no normal distribution. Logistic regression analysis was done to define the risk related to independent variables. A p value of <0.05 was considered to be significant.

Results

Since no mother with eclampsia and acute hypertension developed in the background of chronic hypertension was present in the study group, hypertensive mothers were examined in three groups (preeclampsia, chronic hypertension, and transient hypertension induced by pregnancy).

Demographic findings

During the study, 31 of 63 neonates with a gestational age between 27 and 39 weeks born in our center were considered the study group and 32 of 63 neonates were considered the control group. The perinatal and neonatal properties of a total of 63 subjects constituting the study group and the control group are shown in Table 1.

Table 1 Prenatal–neonatal properties of the subjects
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There was no difference between the groups in terms of maternal age, parity, gestational week, prematurity state, mode of delivery, interventional procedures during pregnancy, meconium, nuchal cord, deceleration, neonatal resuscitation, Apgar scores at the first and fifth minutes, gender and neonatal mortality (p > 0.05). The number of general anesthesia in the study group and the number of spinal anesthesia in the control group was found to be higher. There was a significant difference between the two groups in terms of anesthesia procedures (p = 0.002). Birth weight in the study group was significantly lower compared to the control group (p = 0.008). No labor induction was performed in the pregnant women in either group. In the study group, one subject was lost after delivery because of prematurity and sepsis at the age of 3 days and there was no difference between the two groups in terms of neonatal mortality (p = 0.3). This subject was a newborn born from a preeclamptic mother at the 27th gestational week with a birth weight of 820 g who had neutropenia and thrombocytopenia.

The hypertensive group included 20 (64.5 %) preeclamptic pregnant women, 8 (25.8 %) pregnant women with transient hypertension induced by pregnancy and 3 (9.7 %) chronically hypertensive pregnant women. Mild preeclampsia was present in 14 (70 %) of the preeclamptic mothers and moderate preeclampsia was present in 6 (30 %); 300 mg–3 g/day proteinuria was found in 85 % of the preeclamptic mothers and 3–5 g/day proteinuria was found in 15 %. Three mothers who were hypertensive for more than 6 months were considered to be in the chronic hypertension group. Twenty of 28 mothers with a hypertension period of 3–6 months were preeclamptic mothers and the diagnosis for preeclamptic mothers was made before the 20th gestational week. Eight hypertensive mothers were diagnosed as transient hypertension induced by pregnancy, and hypertension started after the 20th gestational week and returned to normal before the 6th week after delivery in these mothers. Seven of the preeclamptic mothers, one of the mothers with transient hypertension induced by pregnancy, and all of the mothers with chronic hypertension were using anti-hypertensive drugs. Metoprolol was used by chronic hypertensive pregnant women (three women) and nifedipine and α methyl-dopa were used by the pregnant women belonging to the other groups (eight women). No severe side effects were observed with the aforementioned drugs. When the subjects whose mothers used drugs were compared with the subjects who did not use drugs, no significant difference was found in terms of birth weight (1,781 ± 788.3 vs. 2,172.3 ± 679.7 g), Apgar score at the first minute (7.7 ± 2.45 vs. 7.8 ± 1.4) and Apgar score at the fifth minute (8.8 ± 2.2 vs. 9.6 ± 0.8) (p > 0.05).

Complete blood count findings

A hemoglobin value of <13.5 g/dl was considered anemia and a venous hematocrit value of >65 % was considered polycythemia. A neutrophil count of <1,500/mm3 was considered neutropenia, a lymphocyte count of <3,000/mm3 was considered lymphopenia and a thrombocyte count of <150,000/mm3 was considered thrombocytopenia.

Complete blood count parameters of both groups are shown in Table 2 and the state of cytopenic subjects are shown in Table 3.

Table 2 Complete blood count parameters in the subjects of the study group and the control group
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Table 3 Cytopenic subjects in the study group and the control group
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(a) Erythrocyte indices

When the two groups were examined in terms of anemia, the study group included one anemic subject, the control group included three anemic subjects, and no significant difference was found between the two groups in terms of anemia (p = 0.31). None of the groups included polycythemic subjects. When the two groups were compared in terms of erythrocyte indices, no significant difference was found between the two groups in terms of MCV, MCH, and MCHC (p > 0.05). RBC, hemoglobin, RDW, reticulocyte percentage, and the number of normoblasts were significantly higher in the study group compared to the controls (p < 0.05).

(b) Leukocyte indices

Among leukocyte indices, total leukocyte, neutrophil, lymphocyte, monocyte and eosinophil counts were found to be lower in the study group compared to the controls (p < 0.05). No difference was found between the two groups in terms of basophil counts (p > 0.05).

When the two groups were evaluated in terms of cytopenia, 18 neutropenic subjects (4 severely neutropenic, 6 moderately neutropenic, 8 mildly neutropenic), 11 lymphopenic subjects, and 4 neutropenic + lymphopenic (1 severely neutropenic, 3 mildly neutropenic) subjects were found in the study group. In the control group, 2 neutropenic subjects and 6 lymphopenic subjects were found. When the cytopenic subjects were examined, the total number of neutropenic subjects in the study group was found to be higher compared to the control group (p < 0.001). Among neutropenic subjects, the numbers of mildly, moderately and severely neutropenic subjects were found to be higher in the study group (p < 0.05). No difference was found between the two groups in terms of the number of lymphopenic subjects (p > 0.05).

(c) Thrombocyte indices

MPV and PDW values were found to be significantly higher in the study group (p < 0.05). Thrombocyte counts in the subjects in the study group were found to be lower compared to the control group (p < 0.001).

When the two groups were evaluated in terms of cytopenia, ten thrombocytopenic subjects were found in the study group. Neutropenia and/or lymphopenia were found in thrombocytopenic subjects. There was no subject with isolated thrombocytopenia. No thrombocytopenic subject was found in the control group. Among ten thrombocytopenic subjects in the study group, one subject had a thrombocyte count of <20,000/mm3 (10 %), one subject had a thrombocyte count of 20,000–50,000/mm3 (10 %) and eight subjects had a thrombocyte count of 50,000–150,000/mm3 (80 %). Conclusively, 25 of 31 subjects (80.6 %) in the study group and 8 of 32 subjects (25 %) in the control group were cytopenic. The number of cytopenic subjects was found to be higher in the study group compared to the controls (p < 0.001).

When the subjects in the study group were evaluated in terms of complete blood count parameters between themselves, no significant difference was found between hypertensive groups (preeclampsia, chronic hypertension, and transient hypertension induced by pregnancy) (p > 0.05).

Prematurity and premature subjects

When prematurity was examined in cytopenic subjects, 15 of 18 neutropenic subjects, 8 of 11 lymphopenic subjects, 3 of 4 neutropenic + lymphopenic subjects and 9 of 10 thrombocytopenic subjects were premature in the study group. Both neutropenic subjects and 5 of 6 lymphopenic subjects were premature in the control group. While 20 of 25 cytopenic subjects (80 %) were premature in the study group, 7 of 8 cytopenic subjects (87.5 %) were premature in the control group.

When premature subjects were examined, the total number of neutropenic subjects (15 vs. 2) (p < 0.001), the number of moderately neutropenic subjects (4 vs. 0) (p = 0.05) and the number of thrombocytopenic subjects (9 vs. 0) (p = 0.004) was found to be higher in the study group. No significant difference was found between the two groups in terms of the number of mildly neutropenic subjects (6 vs. 2), the number of lymphopenic subjects (8 vs. 5) and the number of neutropenic + lymphopenic subjects (3 vs. 0) (p > 0.05).

Cytopenia was present in 20 of 25 premature subjects (80 %) in the study group and in 7 of 22 premature subjects (31.8 %) in the control group. When the rates of cytopenia of premature subjects were compared, the number of cytopenic subjects was again found to be higher in the study group compared to the controls (p = 0.002). In the study group, birth weight of neutropenic subjects was found to be lower compared to non-neutropenic subjects (p = 0.029). No significant difference was found between the lymphopenic and thrombocytopenic subjects of the study group and the neutropenic and lymphopenic subjects in the control group in terms of birth weight (p > 0.05).

Peripheral smear findings

Since fragmented neutrophils were found in the peripheral smear of two subjects in group 2, these subjects were excluded from the evaluation performed in terms of neutrophils. Therefore, peripheral smear findings of the control group were evaluated in 30 subjects in terms of neutrophils and in 32 subjects in terms of erythrocytes and thrombocytes.

(a) Erythrocyte findings

Erythrocyte abnormalities (spherocytosis, anisocytosis, poikilocytosis, and polychromasia) were found in 16 (51.6 %) of 31 subjects in the study group and in 7 (21.9 %) of 32 subjects in the control group. The difference was found to be statistically significant (p = 0.014).

(b) Leukocyte findings

There was no significant difference in terms of neutrophil hypersegmentation (p > 0.05). Mean number of lobes and abnormality in the segmentation index were found with a higher rate in the study group compared to the controls (p < 0.05). Nuclear structural defects were found in 96.7 % of the study group and in 56.6 % of the control group. This difference was considered to be significant (p < 0.001). The appearance of a defective nucleus was caused by nuclei with hook, lump, and flag-like projections (Table 4).

Table 4 Comparison of peripheral smear findings of neutrophils in the study group and the control group
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Cytoplasmic granular defect was found in 61.3 % of the study group and in 31.2 % of the control group. This difference was significant (p = 0.017). Similarly, membrane abnormality, was found with a significantly higher rate in the study group compared to the controls (35.5 % vs. 6.3 %, p = 0.004). In the evaluation of dysplastic findings performed by counting 100 neutrophils, defective nucleus (7.4 ± 2.9 vs. 1.8 ± 1.6), granular distribution abnormality (2.7 ± 4 vs. 0.9 ± 1.3), and cytoplasmic membrane protrusion (0.8 ± 0.7 vs. 0.03 ± 0.2) were found with a higher rate in the study group (p < 0.05). There was no significant difference between the two groups in terms of hypogranulation, which is one of the cytoplasmic defects (0.06 ± 0.2 vs. 0.09 ± 0.4), agranulation (0.03 ± 0.2 vs. 0), and loss of integrity of cytoplasmic membrane (0.7 ± 1.4 vs. 0.3 ± 1.1) (p > 0.05).

(c) Thrombocyte findings

Although the thrombocyte count was lower and MPV and PDW values were found to be higher in the study group, peripheral smears revealed giant thrombocytes only in three subjects in the study group, the percent of giant thrombocytes in these three subjects was 1 %, and thrombocyte counts were <100,000/mm3. No difference was found between the two groups in terms of percentages of giant thrombocytes (0.1 ± 0.3 vs. 0) and the number of subjects with giant thrombocyte (3 vs. 0) (p = 0.07). No difference was found between hypertensive groups in terms of peripheral smear findings when the subjects in the study group were evaluated between themselves (p > 0.05).

Vitamin B12, folate, ferritin

When serum vitamin B12, folate and ferritin levels were compared between the two groups, no difference was found (p > 0.05) (Table 5).

Table 5 Vitamin B12, folate and ferritin levels and hemoblobin electrophoresis in the study group and the control group
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Hemoglobin electrophoresis

When the two groups were compared in terms of hemoglobin electrophoresis, Hb F levels were found to be significantly higher and Hb A levels were found to be significantly lower in the study group compared to the controls (p < 0.001). There was no significant difference between the two groups in terms of HbA2 (p > 0.05) (Table 5).

Follow-up of the subjects

When the subjects of both groups were evaluated in terms of infections which occurred during a 1 year period, the number of infections diagnosed by a physician was found to be higher in the study group compared to the control group (6.7 ± 4.6 vs. 0.9 ± 1.1, p < 0.001) (Table 6). When the infections were classified, the numbers of upper respiratory infections (4.7 ± 3.4, vs. 0.7 ± 1, p < 0.001), urinary infections (0.9 ± 1.3 vs. 0.1 ± 0.2, p < 0.001), and acute bronchiolitis (0.7 ± 1.9 vs. 0.1 ± 0.2, p = 0.005) were found to be higher in the study group compared to the control group. There was no significant difference between the two groups in terms of the number of gastroenteritis (0.2 ± 0.6 vs. 0.1 ± 0.4, p = 0.2).

Table 6 Comparison of the numbers of infections which occurred in the subjects in the study group and the control group during a 1-year follow-up
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Occurrence of more than eight upper respiratory infections in 1 year is defined as frequent infections. It was observed that the number of frequent infections was higher in the study group compared to the control group (9 vs. 0, p < 0.001). Six of nine subjects with frequent infections were found to be neutropenic at birth (three mildly neutropenic, two moderately neutropenic, and one severely neutropenic) and three were found to be neutropenic + lymphopenic. Peripheral smears revealed nuclear structure defects in all subjects, cytoplasmic granule defects in 6 subjects and membrane abnormalities in four subjects.

Follow-up blood values were examined in 10 of 22 cytopenic subjects in the study group. All of these ten subjects were neutropenic at the time of birth (seven neutropenic +thrombocytopenic, three neutropenic + thrombocytopenic +lymphopenic). Blood samples were taken at the age of 1 month from two of these subjects, at the age of 2 months from two subjects, at the age of 10 months from one subject and at the age of 1 year from five subjects. Cytopenia was not found in any of the follow-up blood samples obtained from these subjects.

Discussion

The frequency of preeclampsia in pregnant women ranges between 10 and 14 % in primigravid women and between 5.7 and 7.3 % in multigravid women [19]. It is mainly observed during the first pregnancy of young mothers. In our study, hypertensive mothers were found to be in the young population and in their first pregnancies. Although there was no significant difference between the two groups in terms of mode of delivery, general anesthesia was performed with a significantly higher rate in the study group compared to the control group, when the procedure of anesthesia during delivery was evaluated. This difference was thought to arise from the fact that general anesthesia was performed at a higher rate among subjects in the study group, who were expected to have complications at a higher rate.

Early and long-term preeclampsia is reported to lead to a decrease in nutrients nourishing the baby and to IUGR [1]. The most commonly observed problem in the baby was growth retardation. In pregnant women with chronic hypertension, the rates of intrauterine growth retardation and fetal mortality are rather high [18]. In our study, birth weights in the study group were found to be significantly lower in the study group compared to the control group. This finding suggested that hypertension in pregnant women caused uteroplacental failure and this led to low birth weight.

In the study performed by Kurlat et al., the risk of polycythemia was shown to be 12.6-fold higher in babies of hypertensive mothers compared to the general population, and it was proven that maternal hypertension constituted a significant risk for polycythemia independent of fetal growth [12]. It has been reported that normoblasts increase in babies of preeclamptic mothers and this is secondary to uteroplacental hypoperfusion [17]. In different studies, hemoglobin, MCV, MCHC, RDW values, and reticulocyte counts were shown to be higher in newborns of preeclamptic mothers [3, 7]. In our study, the finding that erythrocyte counts, hemoglobin value, reticulocyte percent and normoblast count were significantly higher in babies of hypertensive mothers at the time of delivery can be explained by uteroplacental failure and increase in erythropoesis due to hypoxia. However, no significant difference was found between the two groups in terms of MCV, MCH, and MCHC values.

Preeclampsia is known to be a risk factor for neonatal neutropenia and thus for infections in premature newborns. Koenig and Christensen suggested that neutropenia was caused by a decrease in growth factors which increase neutrophil production, and decrease in response of progenitor cells to growth factors and presence of inhibitor substance inhibiting neutrophil production [10]. These investigators showed that the activity of colony stimulating factor decreased in the placenta of hypertensive mothers and found an inhibitor substance inhibiting neutrophil production in the placenta. However, decrease in the response of progenitor cells to growth factors could not be shown. In another study, Fas–Fas ligand interaction was reported to be involved in leucopenia in preeclampsia [11]. In another study, it was reported that the balance of erythropoesis and granulopoesis shifted to the direction of erythropoiesis, and because of hypoxia and the resulting increase in reticulopoesis in normal hematopoesis regulation, no adequate stem cells remained for granulopoesis and as a result inadequate granulopoesis was observed and dysgranulopoesis developed [13]. In our study, total counts of leukocytes, neutrophils, lymphocytes, monocytes, and eosinophils were found to be significantly lower in the hypertensive group. These findings are thought to be caused by one or more of the aforementioned mechanisms.

In newborns of preeclamptic mothers, the incidence of thrombocytopenia was shown to be higher compared to the newborns of normotensive mothers [4, 16]. Although the patophysiologic mechanism underlying thrombocytopenia is not clear, there are studies reporting that it arises from pathology at the placental level [14]. In these studies, it was reported that thrombocytopenia could occur as a result of thrombocyte adherence to the damaged endothelial region caused by segmental vasospasma and vasodilatation in the placenta of hypertensive mothers. Kleckner et al. reported that abnormal placental endothelial surface caused thrombocyte destruction and the resulting thrombocytopenia improved in a short time after delivery [9]. It was also reported that an undefined factor which leads to DIC was transported to the baby by the placenta and caused thrombocytopenia in the newborn [14]. In our study, thrombocyte counts and the number of thrombocytopenic subjects were found to be statistically lower in the hypertensive group. This finding indicates that hypertensive pregnancy is a risk factor for thrombocytopenia in the newborn. The finding that the number of cytopenic subjects was higher in the study group in our study indicates that the newborns of hypertensive mothers carry a higher risk in terms of cytopenia compared to other newborns. The fact that there was no difference between hypertensive groups in the study group in terms of complete blood count parameters suggests that different hypertensive diseases in pregnancy have similar effects in terms of causing cytopenia.

Increase in erythropoiesis, which develops because of uteroplacental failure, and hypoxia can lead to abnormal findings on peripheral smears, including spherocytosis, anisocytosis, and polychromasia [5, 8]. In our study, the aforementioned erythrocyte abnormalities were found on peripheral smear examinations in 51.6 % of the study group and 21.9 % of the control group. These findings support the fact that displastic changes in newborns of hypertensive mothers are observed at a higher rate.

Although platelet count was found to be low and MPV and PDW values were found to be high in the study group, no significant difference in peripheral smear examinations between the two groups in terms of percentage of giant thrombocytes suggests that the present thrombocytopenia is caused by the moderate response of bone marrow. The fact that no difference was found between the hypertensive sub-groups in the study group in terms of peripheral smear findings suggests that different hypertensive diseases of pregnancy have similar effects in terms of causing development of cellular dysplasia.

HbF has a higher affinity for oxygen compared to HbA. The reason for this is the fact that HbF does not interact with 2,3-diphosphoglycerate at a significant level, and cells which contain HbF display a higher oxygen affinity and have the advantage of extracting more oxygen from maternal blood by the placenta. There are studies which showed HbF levels were increased in the umbilical cord in preeclampsia, which is one of the diseases leading to uteroplacental failure, and hypoxia, in addition to studies which showed that HbF levels were increased also in maternal blood [15, 20]. In our study, HbF levels were found to be significantly higher in the hypertensive group compared to the control group and HbA levels were found to be low. This finding was thought to be caused by the stress developed in the fetus by uteroplacental failure and hypoxia.

When the subjects in both groups were evaluated in terms of infections during a 1-year period, it was observed that the number of infections diagnosed by a physician was significantly higher in the study group compared to the control group. Most babies (72.2 %) who had more frequent infections were found to be neutropenic at birth. In these babies lymphopenia was found at a lower rate (22.2 %). Nuclear structure defects were found in all of them, cytoplasmic granule defects were found in 66.6 % and membrane abnormalities were found in 38.8 %. This suggests that a positive relation is present between frequent infections and neutropenia, and nuclear and cytoplasmic dysplastic changes in neutrophils at birth.

In conclusion, birth weights were found to be lower in newborns of hypertensive mothers because of uteroplacental failure and hypoxia compared to the control group and HbF levels, and erythrocyte counts and Hb levels were found to be higher. However, it was observed that neutropenia, thrombocytopenia, and dysplastic changes in neutrophils, and erythrocytes on peripheral smears were found at a higher rate in newborns of hypertensive mothers. Newborns of hypertensive mothers carry a risk for complications including primarily infection and bleeding. Therefore, hematologic follow-up should be performed in these newborns. Complete blood counts and peripheral smear examinations are significant laboratory tests which can be used for early diagnosis of hematologic complications in the newborn which may be caused by hypertensive pregnancies.