Thrombophilia and newborn

: Introduction: The term thrombophilia (TF) describes disorders associated with an increased predisposition of developing venous thromboembolism. Thrombotic accidents during pregnancy are now widely recognized as a cause of morbidity and mortality. Objectives: To compare maternal and term newborn (NB) characteristics between healthy and thrombophilic pregnancies. Methods: The study included 31 full-term newborns whose mothers were diagnosed with TF before the current pregnancy and treatment was carried out through it. In the control group were included 37 full-term NBs. NB indicators which were used are gender, gestation age, birth weight, Apgar score, morbidity during the early neonatal period, hospital stay, treatment during the early neonatal period. The indicators for the mothers are the type of TF, mechanism of childbirth, sequence of pregnancy and sequence of childbirth. Results: In the observed groups of patients, we found that mothers with TF have an average higher age and have a higher number of unsuccessful pregnancies. Тhey more often give birth by operation. The higher the number of maternal TF mutations, the more unsuccessful pregnancies. The NB of mothers with TF have a lower Apgar score, develop RDS more often during the early neonatal period and need a larger volume of therapeutic manipulations and have a significantly longer hospital stay. Conclusions: TF in pregnant women, even when adequate treatment is administered during pregnancy, is associated with increased morbidity in their full-term NBs during the early neonatal period. This requires additional therapeutic measures in full-term newborns and is associated with a prolonged hospital stay.


Introduction:
The term thrombophilia (TF) describes disorders associated with an increased predisposition to develop venous thromboembolism.It was first used by O. Egeberg in 1965 when it described the propensity to venous thrombosis in patients deficient in antithrombin III.Subsequent discoveries of other defects of the hemostasis system and their role in the development thrombotic complications contribute to the use of this term in clinical practice¹⸴²⸴³⸴⁴ .The physiology of pregnancy is characterized by an increase in the synthesis of procoagulant factors (plasma coagulation factors II, VII, VIII, IX, X, fibrinogen, von Willebrand factor), a decrease in blood concentrations and the effects of natural anticoagulants (protein S and C).As a result, the coagulation potentialprothrombotic activity of the bloodis increased, which is evolutionarily necessary to prevent massive obstetric hemorrhages during childbirth and preserve the life of the woman⁵ ⸴⁶ .Thrombotic accidents during pregnancy are now widely recognized as a cause of morbidity and mortality⁷ .The increased risk of blood clotting can be caused by genetic factors, acquired changes in the clotting process or, more often, a combination of hereditary and acquired ones.Hereditary TF is the most common cause of thromboembolism in the mother.It is associated with an increased risk of adverse evolution during pregnancy, including fetal death in the second and third trimesters, abruptio, severe intrauterine fetal International Journal of Medical Science and Clinical Invention, vol.11, Issue 03, March 2024 hypotrophy and early, severe preeclampsia, premature birth⁷ ⸴⁸ .The most prevalent hereditary TF were associated with pathological mutations localized in prothrombin gene mutation (factor II) at position G20210A, factor V Leiden gene mutation (FVL) at position G1691A, methylenetetrahydrofolate reductase (MTHFR) gene mutation at the C677T and A1298C positions and plasminogen activator inhibitor-1 (PAI-1) gene mutation.All these pathological mutations may increase the risk of developing thrombosis ⁹ ⸴¹⁰ ⸴⁴ .The data for the present study were obtained from the patient files of the newborns and their mothers, who were treated in the Department for Newborns and in the Department of Obstetrics, respectively, for the period 2021 -2023.The statistical processing of the data was carried out using a statistical processing program IBM SPSS Statistics version 23 and a spreadsheet program, part of the MS Office -Microsoft Excel package.For a significance level at which the null hypothesis is rejected, p <0.05 was chosen.The following methods were applied: descriptive analysis, tests to establish statistically significant difference, correlation and graphical analysis.

Results:
From the selected 36 parturients with TF and their NBs dropped out 5: one with stillbirth and 4 who gave birth to children before 37 weeks.The average age of the other 31 mothers with TF is 31.4±5.9 years and is significantly higher than the age of the control group B -28.5±4.8 years (p=0.023).In Group A, the share of operative births SC (Cesarean section) is significantly higher -82,7% compared to Group B -37,8% (p=0.004)(Table 1).This difference is at the expense of more operative deliveries in Group A, due to aggravated obstetric history -37,9%, while in Group B this percentage is only 5,4%.The two groups do not differed in the proportion of resections -in Group A 27,6%, in Group B -in 24,3%.
Incorrect presentation/pelvio-fetal disproportion as an indication of SC in the first group was registered slightly more often -13,8%, and in the second groupin 8,1%.Only in one case was an emergency operative birth permit required in Group A (Figure1).The distribution according to the sequence of childbirth is the same in both groups of mothersin 62% it is first and in 38% -second.The average number of pregnancies in women with TF is reliably greater -1.9±1.1, against 1.4±0.5 in the control group of women (p=0.024).The distribution according to pregnancy sequence also shows a significant differencein Group A women with first pregnancy are 52%, second -17%, third -21% and fourth -10%, while in Group B with first are 57%, with second -43% and there are none with third or fourth pregnancy (p=0.024)(Table 1) .The Pearson correlation coefficient for assessing the linear relationship between maternal TF and pregnancy sequence showed a much greater than typical positive correlation (p=(0.034; r=0.787).
Diagnosis TF in 17(55%) of mothers is due to the search for the cause of a previous unsuccessful pregnancy.In 5 (16%) of the mothers of group A, a test for TF was made after establishing such a disease in a close relative.In the course of treatment of infertility and preparation for IVF in 5(16%) cases, TF was proven.Four (13%) of the Group A mothers did their own tests before planning a pregnancy (Table 2).From the collected documentation from pregnancy keeping, it was found that 17(55%) of mothers are carriers of the mutant allele responsible for inhibition of plasminogen activator (PAI -1 5G>4G), 7 are homozygous and 10 heterozygotes.Increased risk of venous thromboembolism due to hyperhomocysteinaemia (decreased activity of the enzyme MTHFR Mutation 677 C>T) was also found in 17(55%) of the studied women, 7 were homozygotes and 10 were heterozygotes.Increased levels of Factor II Prothrombin as heterozygous carrier of the mutant allele (Mutation 20210G>A), were found in one mother.Heterozygotes in the pathological allele for FactorV Leiden (FVL) associated thrombophilia (mutation R506Q) was detected in 5 (16%) cases (Table 3).Some of the patients had more than one form of TF.Using the Pearson correlation coefficient to estimate the linear relationship between established types of TF mutations in mothers and pregnancy sequence, we found a positive correlation (p <0.001; r=0.792) that can be interpreted as much greater than the typical one.When comparing demographic indicators of NB in Group A and Group B, there was no significant difference between them by average birth weight, GA and sex.Children from Group A, however, had a significantly lower score on Apgar score at 1-th and 5-th minutes (7.7±2.1 and 8.7±2.1)compared to those from Group B (8.7±2.1 and 9.6±0.6)(p=0.022,р=0.010) (Table 1).In Group A there is one child with an Apgar score below 7 at 5 minutes, while in Group B there is none.

Plasminogen
A comparison of NB's blood count from the first postnatal day showed no difference in the levels of mean leukocyte counts (Group A -22.8±7.2x10^9/l and Group B -22.4±6.7x10^9/l) and hemoglobin (Group A -176±22g/L and Group B -169±18g/L).Significantly higher were the levels of erythrocytes in Group A (5.0±0.7x10^12/l)compared to Group B (4.2±1.8x10^12/l)(p=0.034).On the other hand, in the NBs from Group A significantly lower average platelet count is registered (Group A 239±59x10^9/l and Group B 305.0±57.9х10^9/l)(p<0.001)(Table 1).Pathology of NBs during an early neonatal period requiring therapy in both groups showed uneven distribution.In Group A, a higher proportion -17(55%) vs. 11(30%) in Group B) of NB who received treatment (p=0.033).In the group of children of mothers with TF, oxygen therapy was much more common 18(59%) compared to the control group 6(16%) (p=0.001).In 3 patients (10%) from Group A, moderately respiratory distress syndrome (RDS) was developed, and in one-severe RDS, while in Group B only one patient with moderate RDS was registered.Verified intraamniotic infection (IAI) requiring an antibiotic course of treatment in Group A was recorded in 10(31%) of children, compared to only 4(11%) from Group B (p=0.041).Parenteral infusion was used significantly more frequently -10(31%) in the first group vs.3 (8%) in the control group (p=0.019).We also reported a significantly longer hospital stay in the patients from Group A -4.6±1.5 days than in Group B -3.6±1.0 days (p=0.002).Using Pearson's correlation coefficient an assessment was made of the linear relationship between maternal TF and morbidity of full-term NBs during the early neonatal period.We found a positive correlation (p=0.004;r=0.348) that can be interpreted as big or even bigger than the typical one.

Discussion:
In the group of patients we observed, we found that mothers with TF have an average higher age and have a higher number of unsuccessful pregnancies.They more often give birth by SC.As the number of mutations for the mother's TF increases, so does the number of unsuccessful pregnancies.The NBs of mothers with TF have a lower Apgar score, develop RDS more often during the early neonatal period and need a larger volume of therapeutic manipulations.These NBs have higher erythrocyte counts and lower platelet counts.For Europe, according to a study by Dugalic et al, the most common forms of TF among the white population are FVL and MTHFR C677T gene mutation.The distribution of the type of TF in our Group A in labor is different, a smaller share is FVL mutations.The most common complications of TF in pregnant women in the European region are recurrent pregnancy loss, abortion, intrauterine fetal death, stillbirth, intrauterine fetal hypotrophy, preeclampsia, placental abruption, venous thromboembolism⁴ .We also have one stillbirth in the initial cohort.In western Romania, observations in 200 mothers with TF found that they faced a significantly increased risk of giving birth to an underweight newborn.Their children had a lower Apgar score, similar to our results.The higher the BMI the mother with TF, the lower the Apgar score of NB ⁷ .
Dusek et al has screened 339 premature NBs with birth weights below 1500 g for carrying mutations for TF in the Czech Republic.They observed the Leiden mutation 2.5 times more frequently compared to the general population¹⁰ .FVL is a disease that does not pose an immediate threat to NBs, however, this risk should not be ignored at a later age, especially in women, when other cumulative risks are present.Routine screening for thrombophilic defects in women without previous pregnancy complications is not currently recommended.However, the prevention of placenta-mediated complications such as recurrent miscarriages, early and late-onset fetal growth restriction, and stillbirth remains a major and topical health problem⁸ .Bremme et al in observation among 38 women with TF and their newborns in Sweden found similar to our results higher age within mothers with TF and a higher proportion of operative delivery in the group with hemostasis disorders.From the NB group, 16% had intrauterine hypotrophy or were SGA.There is one stillbirth.As in our observed TF group, they also had only one patient with an adverse Apgar score at 5 min.The mean NB's weight of mothers with TF was marginally lower compared to the control group, similar to our results ¹⁵ .A study conducted in Cuba among 62 pregnant women and their children showed no association of TF type and maternal age with NB weight, but the later the treatment for TF was initiated, the lower the body weight of NB was²¹.Intrauterine hypotrophy complicates up to 10% of pregnancies, representing a major cause of morbidity and mortality in early childhood.This percentage reaches 25 in third world countries¹².After birth, newborns with intrauterine hypotrophy are at increased risk of hypoglycemia, hypothermia, hyperbilirubinemia, necrotizing enterocolitis, intraventricular hemorrhage, seizures, respiratory distress syndrome, sepsis and neonatal death in extreme cases.Predisposition to certain diseases also remains significant in adulthood, including cognitive or neurological impairment, as well as cardiovascular or endocrine disorders such as stroke, coronary artery disease, dyslipidemia or even diabetes mellitus¹¹⸴²².The risk of thrombosis in NB born after 37 weeks is significantly lower than in premature babies, and the risk of thrombosis correlates with the degree of prematurity: thrombotic complications International Journal of Medical Science and Clinical Invention, vol.11, Issue 03, March 2024 reach their peak in the group of children born 22-27 weeks.A serious risk factor for neonatal thrombosis is the presence of maternal TF and genetic forms of thrombophilia in newborns.Maternal thrombophilia can lead to increased coagulation potential and prethrombotic conditions during pregnancy, causing thrombotic vasculopathy at the placenta level²³⸴²⁴ .In Group A, we associate the low total platelet count with the high proportion of registered congenital infections, because IAI tend to lead to increased consumption of platelets ²⁵ .The higher levels of hemoglobin and erythrocytes on the first postnatal day in Group A are probably related to the lower Apgar score and hypoxemia of the newborns.Polycythemia may be due not only to intrauterine hypotrophy.Due to decreased tissue oxygenation, increased production of erythropoietin by the kidney is followed by an increasing number of erythrocytes and raised fetal blood volume²⁶ .

Limitations of the study
The usual problems discussed in women with thrombophilia and current pregnancy are the risks of birth to premature or hypotrophic children and the pathology that these newborns have.Our retrospective study is of a small group of term neonates who developed with well-controlled maternal thrombophilia.There is clearly a difference in the pathology of the early neonatal period of this group of children.To make a more complete assessment, larger-scale observations and over a longer period of time are needed.

Conclusion:
TF in pregnant women, even when adequate treatment is administered during pregnancy, is associated with increased morbidity in their fullterm NBs during the early neonatal period.This is manifested in a higher Apgar score, delayed cardiopulmonary adaptation, and a higher incidence of infectious pathology.They, in turn, require additional therapeutic measures in newborns and are associated with a prolonged hospital stay.
Scientific searches and observations of pregnancy development against the background of TF are in most cases focused on the causes of intrauterine hypotrophy of the fetus and fetal loss ¹¹⸴¹²⸴¹³⸴¹⁴ .Children born to mothers who have been treated for TF during pregnancy are most likely to have intrauterine hypotrophy, young for gestational age, or born prematurely.Early neonatal health problems can be foreseen by the anamnesis and pathology of the pregnancy in prematural or hypotrophic newborn timely treatment can be carried out¹⁵ ⸴¹⁶ .

International Journal of Medical Science and Clinical Invention, vol. 11, Issue 03, March 2024 Table 1. Demographic and obstetric indicators of the observed groups
(PNpartus normalis, SC -Cesarean section, GAgestation age)