Printer Friendly

Evaluation of serum biomarkers for detection of preeclampsia severity in pregnant women.

Byline: Maryam Kasraeian, Nasrin Asadi, Homeira Vafaei, Tarlan Zamanpour, Hadi Raeisi Shahraki and Khadije Bazrafshan

ABSTRACT

Objectives: To determine serum biomarkers in detection of preeclampsia severity among pregnant women.

Methods: Among 450 pregnant women with various severity of preeclampsia, serum biomarkers ofaspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), hemoglobin (Hb), platelet count (PLT), uric acid, direct bilirubin, total bilirubin, creatinine, and alkaline phosphatase were compared using area under the Receiver operating characteristic (ROC) curve and Area Under the Curve (AUC).

Results: The mean age of women was 30.63+-6.43 years and with mean gestational age of 34.69+-3.97 weeks. The mean level of LDH, ALT, uric acid, and creatinine were significantly higher in the women with severe type of preeclampsia compared to those with mild type. LDH level had ROC and AUC of more than 0.80, with highest sensitivity, and moderatespecificityin comparison to other markers.

Conclusion: Biomarkers such as ALT, uric acid, and LDH were shown to be prognostic in detection of theseverity of preeclampsia. LDH was demonstrated to significantly be a better prognostic test in detection of preeclampsia severity.

KEYWORDS: Biomarker, Preeclampsia,Pregnancy, Severity.

INTRODUCTION

One of the important conditions in pregnant women is hypertensive disorder with serious maternal and fetal complications.1 Among hypertensive disorders, preeclampsia is one of the most important life threatening one for both mothers and neonates worldwide,with 10-15% of the 500,000 maternal deaths each year.2,3 Routine investigation of women with preeclampsia includes determination of liver function test (LFT) including aspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), bilirubin, and albumin levels. There are controversies for association between these parameters and severity of preeclampsia in literature.4

Mean arterial blood pressure, uterine vessels ultrasound,5 serum calcium level6, serum uric acid level,4,6 LDH,7 angiogenesis factors such as placental growth factor (PIGF) and vascular endothelial growth factor (VEGF),2,8 lipid profile,8 and glucose tolerance test9 were previously studied to evaluate the association between these parameters and severity of preeclampsia. In UK, several guidelines were presented for early diagnosis based on assessment of maternal risk factors; including a screening strategy based on maternal history and characteristics by the National Institute of Clinical Excellence (NICE) predicting less than 30% of those developing preeclampsia.10 So there is serious need to assess this association. The present study was undertaken to compare serum biomarkers in pregnant women with different severities of preeclampsiaas prognostic ones in maternal and fetal outcomes.

METHODS

This retrospective study included 450 women with preeclampsia who were referred to Hafez Hospital affiliated to Shiraz University of Medical Sciences from 2005 to 2014. The study was approved by the local Institutional Ethics Review Board (EC-P-9382-8682 dated Feb. 13, 2014). The inclusion criteria for the women with mild preeclampsia were (i) Systolic blood pressure [greater than or equal to]140 mmHg or diastolic blood pressure [greater than or equal to]90 mmHg and (ii) Proteinuria [greater than or equal to]0.3 grams in 24-hour urine specimen. The inclusion criteria for the women with severe preeclampsia11 were:

1. Signs of liver problems (such as vomiting with abdominal pain)

2. Signs of central nervous system problems (such as blurry vision and severe headache)

3. Very high blood pressure (greater than 160 systolic or 110 diastolic)

4. At least twice the normal measurements of certain liver enzymes on blood test

5. Thrombocytopenia

6. Greater than 5g of protein in a 24-hour sample

7. Very low urine output (less than 500mL in 24 hours)

8. Signs of respiratory problems (such as pulmonary edema)

9. Severe fetal growth restriction

10. Stroke

The women with unstable conditions were excluded from the study.Information such as age,gestational age (GA), and serum levels of LDH, hemoglobin (Hb), platelet count (PLT), uric acid, direct bilirubin, total bilirubin, AST, ALT, serum creatinine (SCr), and alkaline phosphatase, were compared between the women with mild and severe preeclampsia.The obtained data were reported as mean+-SD. SPSS software (Version 20, Chicago, IL, USA) was used for statistical analysis. Independent T-test,Pearson's chi-square and Fisher's exact tests were used to compare the groups. Receiver Operating Characteristic (ROC) curve was drawn to specify the optimal cut-off points of the variables for prediction of preeclampsia. Sensitivity, specificity, and the Areas Under the Curves (AUC) were also calculatedwith 95% confidence intervals. A P-value<0.05 was considered as statistically significant.

Table-I: Paraclinical parameters of the pregnant women with severe and mild preeclampsia.

Parameter###Severity of###Mean +- SE###P-value

###preeclampsia

Age(year)###Mild###30.16+-5.96###0.24

###Severe###30.89+-6.76

GA(month)###Mild###37.73+-2.27###<0.001

###Severe###32.67+-3.52

LDH(IU/L)###Mild###337.89+-173.15###<0.001

###Severe###556.41+-193.02

Hb(g/dL)###Mild###11.8+-1.62###0.89

###Severe###11.78+-1.8

PLT(x109.L-1)###Mild###191.18+-49.06###0.019

###Severe###179.08+-56.35

Uric acid###Mild###5.43+-1.2###<0.001

(mg/dL)###Severe###6.2+-1.4

Direct bilirubin###Mild###0.23+-0.08###0.415

(mg/dL)###Severe###0.24+-0.09

Total bilirubin###Mild###0.6+-0.22###0.86

(mg/dL)###Severe###0.6+-0.18

ALT(IU/L)###Mild###18.78+-30.38###0.001

###Severe###32.99+-54.07

AST(IU/L)###Mild###32.45+-50.8###0.07

###Severe###43.54+-73.63

SCr(mg/dL)###Mild###0.84+-0.27###0.017

###Severe###0.9+-0.26

Alkaline###Mild###333.94+-120.61###0.35

phosphatase###Severe###321.42+-147.74

(IU/L)

Table-II: The variables with high area under curve (AUC). The data are presented as point estimation with 95% confidence interval.

Paraclinical parameters###AUC###Cut-off point###Sensitivity###Specificity

LDH###0.805(0.765-0.842)###336###89.62(86.22-93.02)###59.3(51.6-66.7)

Uric acid###0.666( 0.618-0.712)###5.53###68.67(62.5-74.4)###58.54(50.6-66.2)

ALT###0.657( 0.609-0.702)###14.33###62.16(56-68.1)###62.73(54.8-70.2)

AST###0.604(0.556-0.651)###0.25###57.92(51.6-64)###60.49(52.5-68.1)

SCr###0.604( 0.555-0.652)###0.96###29.64(24.1-35.7)###89.1(83.1-93.5)

RESULTS

Out of the 450 women, 180 and 270 ones wereassignedto the mild and severe preeclampsia groups, respectively. Among the 450 births, 221 neonates were male, 217 were female, and 12 were twin male-female neonates. The mean age of pregnant women was 30.63+-6.43 years with the mean GA of 34.69+-3.97 weeks. Out of the 12 women with twin pregnancies, 11 (91.67%) showed severe preeclampsia (P=0.03). No significant association was noted between the neonates' sex and severity of preeclampsia (P=0.49).The comparison of serum biomarkers in pregnant women with mild and severe preeclampsia was presented in Table-I. The two groups were significantly different for GA, LDH, PLT, uric acid, ALT, and SCr.The mean GA of women with mild preeclampsia was higher compared to those with severe preeclampsia (P<0.001). The mean level of PLT was also higher among the mild cases of preeclampsia in comparison to those with severe preeclampsia (P=0.019).

The mean level of LDH, ALT, uric acid, and SCr were significantly higher in the women with severe type preeclampsia compared to those with mild type. The ROC curve for LDH is shown in Fig.1. Findings for variables with higher AUC are presented in Table-II, but for variables with AUC0.80, withthe highest sensitivity, and moderatespecificityin comparison to other tests. ALT,AST, and uric acid denoted to a moderatesensitivity and specificity, while SCr had the highest specificity and the lowest sensitivity among the variables (Table-II).

DISCUSSION

Maternal complications, such as proteinuria, eclampsia, severe hypertension, hemolysis, abnormal LFTs, and low platelet count can result from preeclampsia.12,13 Some biomarkers have also been reported to be significantly associated with preeclampsia during pregnancy.14 Martin et al.15 proposed a protocol for quick hazard assessment of severe preeclampsiashortlyafter meeting study admission criteria evaluating symptoms and levels of AST, ALT, LDH, uricacid, proteinuria, and creatinine.The differences in SCr level between the normal pregnant women and those suffering from preeclampsia were shown not to be significant.16 Our results were in line with the study presented an increased level of SCr in preeclampsia women compared to those with normal pregnancy.17 Our findings revealed that SCr test was poorly sensitive and had the lowestpredictive value to differentiate the severity of preeclampsia.

Uric acid level, as a marker of oxidative stress, tissue injury, and renal dysfunction, is increased in hypoxia and ischemia of the placenta.11 Thus, measuring serum uric acid may be used to predict preeclampsia and the mean level of uric acid can be associated with the severity of preeclampsia.18 Alavi et al.6 found a significant difference for serum calcium and uric acid between the normal pregnant women and those with signs of preeclampsia. In 2009, serum uric acid was found to predict maternal complications in management of preeclampsia under realistic assumptions. It was demonstrated that preeclamptic patients with increased serum uric acid values had to undergo induced labor due to their increased risk of complications.13 Similarly, our results showed a higher mean level of maternal serum uric acid in women with severe preeclampsia in comparison to those with mild type (P 0.70 and were modestly predictive tests to show adverse maternal outcomes in women with preeclampsia. In agreement with Kozic et al.4, our finding demonstrated that LDH level had ROC and AUC > 0.80, with the highest sensitivity, and moderatespecificityin comparison to other tests.

The study by Peralta et al.29 showed a significant difference between the mild and severe preeclampsia patients and healthy controls regarding LDH level too. In the present study, LDH levelsignificantly raised based on the severity of the disease (P<0.001).

Limitations of the study: It included lack of a normal and healthy control group and lack of attention to the patients' trimester of pregnancy as there are different strategies in prediction of preeclampsia in each trimester.

CONCLUSION

We canconclude that ALT, uric acid, and LDH levelscan be predictivefactors in identification and categorization of the severity of preeclampsiain pregnant women, even LDH level had the highest sensitivity and moderate specificity in comparison to other parameters.

ACKNOWLEDGMENTS

The authors are grateful to Shiraz University of Medical Sciences for financial support. The authors are also grateful to Mohsen Varzande for editing and improving English language in the manuscript.

Conflict of Interest: The authors declare that they have no competing interest.

REFERENCES

1. Hu WS, Feng Y, Dong MY, He J.Comparing maternal and perinatal outcomes in pregnancies complicated by preeclampsia superimposed chronic hypertension and preeclampsia alone.Clin Exp Obstet Gynecol. 2016;43:212-215.

2. Kar M. Role of biomarkers in early detection of preeclampsia. J Clin Diagn Res. 2014;8:BE01-BE04. doi: 10.7860/jcdr/2014/7969.4261.

3. Khan KS, Wojdyla D, Say L, Gulmezoglu AM, Van Look PF. WHO analysis of causes of maternal death: a systematic review. Lancet. 2006;367:1066-1074. doi: 10.1016/S0140-6736(06)68397-9.

4. Kozic JR, Benton SJ, Hutcheon JA, Payne BA, Magee LA, von Dadelszen P, et al. Abnormal liver function tests as predictors of adverse maternal outcomes in women with preeclampsia. J Obstet Gynaecol Can. 2011;33:995-1004. doi: 10.1016/s1701-2163(16)35048-4.

5. Baschat AA, Magder LS, Doyle LE, Atlas RO, Jenkins CB, Blitzer MG. Prediction of preeclampsia utilizing the first trimester screening examination. Am J Obstet Gynecol. 2014;211:514 e1-7.doi: 10.1016/j.ajog.2014.04.018.

6. Alavi A, Jahanshahi K, Karimia S, Arabzadea N, Fallahi S. Comparison of serum calcium, total protein and uric acid levels between hypertensive and healthy pregnant women in an Iranian population. Life Sci J. 2012;9:485-488.

7. Jaiswar SP, Gupta A, Sachan R, Natu SN, Shaili M. Lactic dehydrogenase: a biochemical marker for preeclampsia-eclampsia. J Obstet Gynaecol India. 2011;61:645-648. doi: 10.1007/s13224-011-0093-9.

8. Di Lorenzo G, Ceccarello M, Cecotti V, Ronfani L, Monasta L, Vecchi Brumatti L, et al. First trimester maternal serum PIGF, free beta-hCG, PAPP-A, PP-13, uterine artery Doppler and maternal history for the prediction of preeclampsia. Placenta. 2012;33:495-501. doi: 10.1016/j.placenta.2012.03.003.

9. Parra-Cordero M, Sepulveda-Martinez A, Preisler J, Pasten J, Soto-Chacon E, Valdes E, et al. Role of the glucose tolerance test as a predictor of preeclampsia. Gynecol Obstet Invest. 2014;78:130-135.doi: 10.1159/000358876.

10. Yu CK, Smith GC, Papageorghiou AT, Cacho AM, Nicolaides KH, Fetal Medicine Foundation Second Trimester Screening G. An integrated model for the prediction of preeclampsia using maternal factors and uterine artery Doppler velocimetry in unselected low-risk women. Am J Obstet Gynecol. 2005;193:429-436.doi: 10.1016/j.ajog.2004.12.014.

11. Practice ACoO. ACOG practice bulletin. Diagnosis and management of preeclampsia and eclampsia. Number 33, January 2002. American College of Obstetricians and Gynecologists. Int J Gynaecol Obstet. 2002;77:67-75. doi: 10.1016/s0020-7292(02)80002-9.

12. van Oostwaard MF, van Eerden L, de Laat MW, Duvekot JJ, Erwich J, Bloemenkamp K, et al. Maternal and neonatal outcomes in women with severe early onset pre-eclampsia before 26 weeks of gestation, a case series. BJOG. 2017;124:1440-1447. doi: 10.1111/1471-0528.14512.

13. Koopmans CM, van Pampus MG, Groen H, Aarnoudse JG, van den Berg PP, Mol BW. Accuracy of serum uric acid as a predictive test for maternal complications in pre-eclampsia: bivariate meta-analysis and decision analysis. Eur J Obstet Gynecol Reprod Biol. 2009;146:8-14.doi: 10.1016/j.ejogrb.2009.05.014.

14. Allen RE, Rogozinska E, Cleverly K, Aquilina J, Thangaratinam S. Abnormal blood biomarkers in early pregnancy are associated with preeclampsia: A meta-analysis. Eur J Obstet Gynecol Reprod Biol. 2014;182:194-201.doi: 10.1016/j.ejogrb.2014.09.027.

15. Martin JN Jr., May WL, Magann EF, Terrone DA, Rinehart BK, Blake PG. Early risk assessment of severe preeclampsia: admission battery of symptoms and laboratory tests to predict likelihood of subsequent significant maternal morbidity. Am J Obstet Gynecol. 1999;180:1407-1414.doi: 10.1016/s0002-9378(99)70026-8.

16. Salako BL, Odukogbe AT, Olayemi O, Adedapo KS, Aimakhu CO, Alu FE, et al. Serum albumin, creatinine, uric acid and hypertensive disorders of pregnancy. East Afr Med J. 2003;80:424-428.

17. Manjareeka M, Nanda S. Elevated levels of serum uric acid, creatinine or urea in preeclamptic women. Int J Med Sci Public Health. 2013;2:43-47.doi: 10.5455/ijmsph.2013.2.43-47.

18. Bainbridge SA, Roberts JM. Uric acid as a pathogenic factor in preeclampsia. Placenta. 2008;29SupplA:S67-72.doi: 10.1016/j.placenta.2007.11.001.

19. Roberts JM, Bodnar LM, Lain KY, Hubel CA, Markovic N, Ness RB, et al. Uric acid is as important as proteinuria in identifying fetal risk in women with gestational hypertension. Hypertension. 2005;46:1263-1269. doi: 10.1161/01.HYP.0000188703.27002.14.

20. Thangaratinam S, Ismail KM, Sharp S, Coomarasamy A, Khan KS. Tests in Prediction of Pre-eclampsia Severity review g. Accuracy of serum uric acid in predicting complications of pre-eclampsia: a systematic review. BJOG.2006;113:369-378. doi: 10.1111/j.1471-0528.2006.00908.x.

21. Williams KP, Galerneau F. The role of serum uric acid as a prognostic indicator of the severity of maternal and fetal complications in hypertensive pregnancies. J Obstet Gynaecol Can. 2002;24:628-632. doi: 10.1016/s1701-2163(16)30193-1.

22. Choi HK, Liu S, Curhan G. Intake of purine-rich foods, protein, and dairy products and relationship to serum levels of uric acid: the Third National Health and Nutrition Examination Survey. Arthritis Rheum. 2005;52:283-289.doi: 10.1002/art.20761.

23. Li S, Sanna S, Maschio A, Busonero F, Usala G, Mulas A, et al. The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. PLoS Genetics.2007;3:e194. doi: 10.1371/journal.pgen.0030194.

24. Burwick RM, Feinberg BB. Eculizumab for the treatment of preeclampsia/HELLP syndrome. Placenta. 2013;34:201-203. doi: 10.1016/j.placenta.2012.11.014.

25. Thangaratinam S, Koopmans CM, Iyengar S, Zamora J, Ismail KM, Mol BW, et al. Accuracy of liver function tests for predicting adverse maternal and fetal outcomes in women with preeclampsia: a systematic review. Acta Obstet Gynecol Scand. 2011;90:574-585.doi: 10.1111/j.1600-0412.2011.01112.x.

26. Demir SC, Evruke C, Ozgunen FT, Urunsak IF, Candan E, Kadayifci O. Factors that influence morbidity and mortality in severe preeclampsia, eclampsia and hemolysis, elevated liver enzymes, and low platelet count syndrome. Saudi Med J. 2006;27:1015-1058.

27. Hall DR, Odendaal HJ, Kirsten GF, Smith J, Grove D. Expectant management of early onset, severe pre-eclampsia: perinatal outcome. BJOG. 2000;107:1258-1264.

28. Qublan HS, Ammarin V, Bataineh O, Al-Shraideh Z, Tahat Y, Awamleh I, et al. Lactic dehydrogenase as a biochemical marker of adverse pregnancy outcome in severe pre-eclampsia. Med Sci Monit. 2005;11:CR393-CR397.

29. Peralta Pedrero ML, Basavilvazo Rodriguez MA, Cruz Avelar A, Sanchez Ambriz S, Guzman Ibarra Mde L, Martinez Garcia Mdel C. [Clinical significance of the laboratory determinations in preeclamptic patients]. Ginecol Obstet Mex. 2004;72:57-62.
COPYRIGHT 2018 Asianet-Pakistan
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Publication:Pakistan Journal of Medical Sciences
Article Type:Report
Geographic Code:9TAIW
Date:Aug 31, 2018
Words:3124
Previous Article:Predictors of serious findings on bi-directional endoscopy in young patients with anemia and GI symptoms.
Next Article:Efficacy of Vitamin D supplementation in achieving an early sputum conversion in smear positive Pulmonary Tuberculosis.
Topics:

Terms of use | Privacy policy | Copyright © 2024 Farlex, Inc. | Feedback | For webmasters |