Introduction
Preeclampsia is a maternal syndrome with the symptoms such as hypertension, proteinuria, and edema after 20th weeks of pregnancy.1 The symptoms of preeclampsia include persistent headache, blurred vision, vomiting, and abdominal pain.2 It may complicate the pregnancy by leading to fetal uterine growth restriction, preterm delivery, maternal and fetal morbidity and mortality.3,4 Preeclampsia is a leading cause of hypertension and complicates up to 10% of the pregnancy.5 In the hypertensive disorders, preeclampsia and eclampsia have huge impact on the maternal and fetal morbidity and mortality. In Indian scenario, preeclampsia and eclampsia accounts for 24% of the maternal deaths.6 The incidence of preeclampsia alone in India is reported to be 8-10% among the pregnant women. It usually occurs during the second half of the pregnancy. Pre-eclampsia is more common in primigravida women than the second or later pregnancies.7
Although exact cause of preeclampsia is unknown, evidences on placenta playing a role in the pathophysiology have become significant. Shallow endovascular cytotrophoblast invasion in spiral arteries, inappropriate endothelial cell activation and an exaggerated inflammatory response are key features in the pathogenesis of preeclampsia.8 Pathological placental specimen in preeclampsia shown infarcts by ischemia, occlusion of spiral arteries and failure of vascular remodeling of spiral arteries by trophoblastic cells. This is life threatening for mother and fetus by vasospasm, endothelial dysfunction and ischemia. As a consequence of possible etiological factors, several disturbances in the mother is reason for preeclampsia, which includes changes in hemodynamic, cardiovascular, hematological, endocrine, liver, kidney functions, cerebrovascular, neurological and visual activity.9
Serum lactate dehydrogenase (LDH) and serum gamma glutamyl transferase (GGT) have no metabolic functions in the extracellular space. But its level indicates the disturbance. Altered endothelial function play important role in pathogenesis of preeclampsia. Intra cellular enzyme such as LDH increased in serum of preeclamptic women due to cellular death. It is also used to assess the presence of tissue damage. GGT present in many tissues particularly in liver.10
Objective of the study was to determine serum lactate dehydrogenase and serum gamma glutamyl transferase as biochemical markers in preeclamptic pregnant women and its comparison with normal pregnant women in third trimester. Also, to find the role of Hb in preeclampsia.
Materials and Methods
Study designed was o bservational prospective case control which was confined to R L Jalappa Hospital and Research Centre, Tamaka, Kolar. The duration of the study was three years (August 2013 to August 2016)11. Ethical Clearance was obtained from Institutional Ethics Committee of Sri Devaraj Urs Medical College. The study population enrollment was commenced after obtaining patient written informed consent. The study was conducted in collaboration with Department of Obstetrics and Gynecology.
All pregnant women after 20 weeks of gestation with preeclampsia diagnosed as per National High Blood Pressure Education Programme working group (NHBPEP) classification admitted with singleton pregnancy, no fetal anatomical anomaly, nonsmokers were included in the study at R L Jalappa Hospital and Research Center. Pre-eclampsia was diagnosed with blood pressure of ≥140/90 mm of Hg noted for the first time during pregnancy on ≥2 occasions at least 4 hours apart, after 20 weeks of gestation with proteinuria of ≥300 mg/24 hours or ≥ 1+. History of renal disease, history of thyroid disorder, history of chronic hypertension, history of gestational diabetics, history of epilepsy, history of hypertensive encephalopathy, history of cardio vascular disease and multigravida were excluded. 50 preeclamptic women and 50 normotensive pregnant women in the third trimester and age between 18-35 were included in the study.
Four ml of blood was collected and aliquoted from the non-pregnant, normotensive pregnant and preeclamptic women visited department of obstetrics and gynecology. Blood samples were collected and centrifuged at 3000 rpm for 10 minutes to obtain the clear plasma and serum. Thus, obtained clear sera and plasma were stored at -80 ˚C until analysis.
Protein in random urine was estimated by dipstick method. Gamma glutamyl transferase activity was determined by a coupled enzyme assay, in which Gamma glutamyl transferase transfers the Gamma glutamyl group from the substrate L-Gamma glutamyl-p-nitroanilide releasing the chromogen p-nitroanilide. The chromogen p-nitroanilide was measured colorimetrically at 418nm. The intensity of the colour is directly proportional to the amount of the GGT present. Lactate dehydrogenase was measured by spectrophotometric method where lactate is converted to pyruvate with simultaneous reduction of NAD to NADH which was measured colorimetrically at 450nm.
Result
The demographic characteristics such as age distribution of the normotensive pregnant and preeclampsia were depicted in percentage. Table 1 shows that 25% of the normal pregnant population were in the 18-20 age group and 24% had preeclampsia. In 21-25 age group 56% were normotensive pregnant and 51% were in preeclampsia group.26-30 age group 17% were normotensive and 16% were in preeclampsia with age group more than 30, 2% were in normotensive and 9% had preeclampsia.
Table 1
| Age in years | Normotensive pregnant (n=50) | Preeclampsia (n=50) |
| Percentage | Percentage | |
| 18-20 | 25 | 24 |
| 21-25 | 56 | 51 |
| 26-30 | 17 | 16 |
| >30 | 2 | 9 |
Age distribution of the subjects under the study groups
Table 2
| Gestational age in weeks | Normotensive pregnant (n=50) | Pre-eclampsia (n=50) | |
| Percentage | Percentage | ||
| 28-33 | 4 | 16 | |
| 34-37 | 14 | 25 | |
| 38-40 | 82 | 59 | |
| >40 | 0 | 0 | |
Gestational age distribution of the subjects under the study groups
The distribution of gestational age for the subjects of normotensive pregnant and preeclampsia were represented as percentage. Gestational week between 34-37 shows 14% ormotensive and 25% preeclamptic. Gestational week between 38-40 week had 82% normotensive and 59% preeclampsia.
Table 3 shows that systolic blood pressure, diastolic blood pressure, LDH and GGT had P value<0.001. Haemoglobin has not showed significance between normal pregnant women and preeclampsia levels between mild and severe preeclampsia.
Table 3
Showing biochemical parameters in preeclampsia and healthy pregnant women
Discussion
Our finding shows that women with more than 30 age groups are at increased risk of getting preeclampsia compared to the normal pregnant women. Previous studies reported teenage pregnancy and increased maternal age increases risk of preeclampsia.12 We found preterm delivery is the major consequence of preeclampsia which goes with literature.13 Odul AA et al showed high maternal haemoglobin concentration in normotensive women associated with IUGR. But in our studies we found no difference in haemoglobin levels in normotensive pregnant women and preeclampsia.14
GGT and LDH significantly increased in preeclampsia group when compared to normal pregnant women.13 Study conducted by Amburgey showed increase in haemoglobin levels in preeclampsia but in the present study found no change in haemoglobin levels.15,16
Normal placentation involves extensive implantation of spiral arterioles which were invaded by endovascular trophoblast that replaces vascular endothelial and muscular linings leading to the enlargement of the vessel diameter. Abnormal placentation involves incomplete trophoblastic shallow invasion which fails to replace vascular endothelial cell and muscular linings. The defective trophoblastic invasion leads to the constriction of spiral arteries and diminish the vessel diameter compare to normal placentation. Thus, leads to the varied oxygenation in placenta generating free radicals and oxidative stress. As compensatory mechanism to hypo perfusion and oxidative stress, placenta releases factors in to the circulation which may results in systemic alterations.17,18 Ischemic placenta contributes to the endothelial dysfunction by altering circulating levels of angiogenic and antiangiogenic factors. Endothelial cell dysfunction may be also due to activated leukocytes by cytokines which adds to the oxidative stress and destructs the endothelial cells.19,20 In preeclampsia, cellular dysfunction leads to the LDH leakage to the extracellular space. GGT is a microsomal enzyme its levels increases in hepatic injury.21 However in the current study the increased GGT levels shows that not only by hepatic origin but its levels are a lso increased in tissue damage in preeclampsia.
Conclusion
In preeclampsia, vascular endothelial damage may lead to multi organ dysfunctions leads to excessive LDH leakage and elevated levels in serum due to cellular dysfunction. GGT is increased in hepatic injury, however in the current study the increased GGT levels shows that not only by hepatic origin but its levels are also increased in tissue damage during preeclampsia as a major cause of endothelial vascular damage. Elevated levels of serum LDH and serum GGT indicates the tissue damage related to endothelial vascular damage and is the main cause of preeclampsia.
