Printer Friendly

Can we predict severity of intrahepatic cholestasis of pregnancy using inflammatory markers?/Enflamatuvar belirtecleri kullanarak gebelik kolestazinin ciddiyeti ongorulebilir mi?

Introduction

Intrahepatic cholestasis of pregnancy (ICP) is the most common liver disease seen during pregnancy, with a changing prevalence worldwide (1,2). The etiology and pathogenesis of ICP are multifactorial. Environmental factors, nutritional deficiencies, hormonal changes, and genetic variations have been found to be responsible for ICP (3,4). It presents most often in the form of pruritus in the second and third trimesters of pregnancy, with elevated serum aminotransferases and/or elevated serum bile acid levels ([greater than or equal to]10 [micro]mol/L) (5). ICP can be differentiated from other types of liver diseases unique to pregnancy that share similar laboratory abnormalities such as preeclampsia, acute fatty liver of pregnancy, and hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome (1,6,7). In addition, other skin diseases that cause high transaminase levels in pregnancy must be excluded. After delivery, the symptoms of ICP usually resolve within 48 hours, with laboratory abnormalities normalizing within 2-8 weeks (8,9).

Bile acid levels can affect perinatal outcomes and are related to an increased risk of iatrogenic preterm delivery, spontaneous preterm delivery, meconium-stained amniotic fluid (MSA), and sudden intrauterine death of the fetus (8,10-12). In the severe ICP group, the incidence of complications is higher than in the mild group (8). Unfortunately, ultrasonography, cardiotocography, fetal movements, and Doppler ultrasonography cannot predict fetal death; there is no perfect test or prognostic marker available to predict fetal outcome (8,13,14).

Recent studies demonstrated the prognostic role of inflammatory markers in both cardiovascular diseases and malignancies (15,16), but few studies have been performed with ICP. The neutrophil-to-lymphocyte (NLR) ratio, platelet-to-lymphocyte (PLR) ratio, mean platelet volume (MPV), and red blood cell distribution width (RDW) are hematologic inflammatory markers. One important pathogenesis responsible for the occurrence of ICP is inflammation; however, it is not known which mechanism initiates this inflammation (17). Recently, NLR has been found to be a promising diagnostic marker in ICP (18). To the best of our knowledge, no studies have investigated the roles of PLR and RDW in ICP. Therefore, we aimed to evaluate the role of inflammatory markers, which are readily available and easily calculated parameters, in the severity of ICP.

Materials and Methods

This retrospective case-control study was conducted at Zeynep Kamil Women and Children's Health Training and Research Hospital, Istanbul. Patients with ICP who delivered their babies in this hospital from January 2013 to January 2016 were enrolled in this study. All data were obtained from hospital files and our computer database. This study was approved by the Zeynep Kamil Women and Children's Health Training and Research Hospital Local Ethics Committee (approval number: 136). The term ICP was used if the serum bile acid level was [greater than or equal to]10 [micro]mol/L with pruritus that could not be explained by any other condition. A total of 102 women with ICP were enrolled in this study. The exclusion criteria were: patients with incomplete data, fetal congenital anomalies, multiple pregnancies, chronic/acute liver disease (Wilson's disease, cholecystitis, primary sclerosing cholangitis, primary biliary cirrhosis, alpha-1-antitrypsin deficiency, symptomatic cholelithiasis, cytomegalovirus, Epstein-Barr virus, autoimmune hepatitis, or acute fatty liver of pregnancy), and HELLP syndrome. A total of 84 singleton pregnancies were included in this research.

The patients with ICP were categorized into two groups according to their serum bile acid levels: mild (<40 [micro]mol/L, n=53) and severe ([greater than or equal to]40 [micro]mol/L, n=31). The control group was selected from age-matched healthy women who had singleton deliveries on the same day as that of patient's with ICP. All gestational age-matched controls complied with the exclusion criteria (n=145).

Serum bile acids were evaluated using an enzymatic assay with intra and inter-assay precisions of 3% and 4%, respectively, [Diazyme Total Bile Acids (TBA) kit; Diazyme Diagnostic Laboratories, USA] and a Cobas C501 (Roche, USA). A blood analyzer (Cell-Dyn 3700; Abbott, USA) was used to determine the complete blood cell count (CBC). The CBC inflammatory markers measured were white blood cell counts (WBC), platelets, NLR, PLR, MPV, and RDW.

Perinatal death was defined as mortality from over 24 weeks' gestation until 7 days postpartum. A low Apgar score was defined as a score of below 7 at 5 minutes. The main outcome of the measures was the association of the inflammatory factors (WBC, NLR, PLR, MPV, and PDW) with the severity of ICP.

Statistical Analysis

The statistical analysis was performed using the Statistical Package for the Social Sciences for Windows version 18 (SPSS Inc., Chicago, IL, USA). A p value of less than 0.05 was accepted as being statistically significant, and all measurements were performed within a 95% confidence interval. The results of the study are expressed as means, standard deviations, and percentages. According to the data distribution, comparisons were made using Student's t-test, ANOVA, or the chi-square ([chi square]) test, when appropriate. A post-hoc least significant difference test was used after the ANOVA analysis. Relationships between the data were evaluated using Pearson's correlations.

Results

The comparison between the patients with ICP (n=84) and controls (n=145) showed similar ages (28[+ or -]5.5 vs. 28.1[+ or -]5.2 years, p>0.05) and gravidities (2.1[+ or -]1.3 vs. 2.3[+ or -]1.2, p>0.05). The ICP group showed significantly decreased gestational weeks at delivery (36.2[+ or -]2.3 vs. 39.1[+ or -]1.4 weeks, p<0.001) and birth weights (2899[+ or -]623.3 g vs. 3373[+ or -]413.9 g, p<0.001) when compared with the healthy controls. The comparison of the characteristic findings of the patients with mild and severe ICP is presented in Table 1. The majority of patients (77.3% mild ICP vs. 74.1% severe ICP) were overweight/obese and aged younger than 35 years (79.2% mild ICP vs. 70.9% severe ICP), respectively. The women with mild and severe ICP exhibited similar characteristics with regard to educational status, chronic disease history, and previous ICP history (p<0.05). Table 2 presents the laboratory findings; with the exception of serum bile acid levels, the women with mild and severe ICP had similar findings.

Serum bile acids were positively and significantly correlated with PLR (r=0.343, p=0.003), but the correlations of bile acids with WBC (r=-0.062), neutrophils (r=-0.198), lymphocytes (r=-0.112), MPV (r=0.08), RDW (r=-0.174), and NLR (r=-0.110) were statistically non-significant (p>0.05). Serum bile acids were negatively significantly correlated with gestational age at delivery (r=-0.390, p<0.001) and birth weight (r=-0.252, p=0.02), and PLR was negatively correlated with gestational age at delivery (r=-0.254, p=0.003).

The comparison of the obstetric outcomes in the women with mild and severe ICP is given in Table 3. The percentages of those having male fetuses, low Apgar scores, fetal distress, MSA, preeclampsia, perinatal/neonatal mortality, gestational diabetes, Rh isoimmunization, and abortus imminence were similar between the women with mild and severe ICP. However, the gestational age at delivery and time of diagnosis were earlier in the severe group (p<0.05). In addition, the cesarean section rate was significantly increased in the severe group (p<0.05).

Table 4 shows the comparison of the inflammatory markers between the normal and ICP groups. Overall, the inflammatory markers were significantly increased in the ICP group, including WBC, MPV, and PLR (p<0.05), and neutrophils, lymphocytes, and RDW were significantly decreased in the ICP group (p<0.05). However, NLRs were similar between the normal and ICP groups.

Table 5 presents the comparison of the inflammatory markers in the healthy controls and women with mild and severe ICP. The RDW (p=0.128) and WBC (p=0.535) values were similar between the women with mild and severe ICP. MPV was significantly increased in the severe ICP group when compared with controls and the mild ICP group (p<0.05). Despite the fact that PLR was increased and RDW was decreased in patients with ICP, they were not significantly changed between the mild and severe groups. MPV was the marker that significantly increased in the severe group.

Discussion

ICP is a liver disease of pregnancy that increases fetal mortality; therefore, early diagnosis and assessment of the severity of the disease is an important task. In this study, we aimed to investigate the associations between the readily available, but newly defined, inflammatory markers, NLR, PLR, MPV, and RDW, with the severity of ICP. The present study found that the inflammatory markers were significantly increased in patients with ICP, and that MPV increased with the severity of ICP. Fetal distress, premature delivery, perinatal asphyxia, and intrauterine fetal death may all occur in patients with ICP (2,8,19), and increased bile acid levels are thought to be the cause of these complications (20). Consistent with previous studies, we observed lower birth weights and more preterm deliveries among patients with ICP (11,21-23). However, there were no significant differences found in maternal age, parity, diabetes history, history of chronic systemic disease, preeclampsia or maternal hepatitis B and C infections in the women with mild and severe ICP, which was consistent with the study by Kawakita et al. (24). Some studies found similar cesarean section rates (12,25,26), in contrast to others (20,27). In our study, cesarean rates were higher with severe ICP. Some authors found an increased MSA risk in the ICP group when compared with controls (8,28,29), but some authors did not support these findings (27). In addition, some previous studies reported an increased MSA risk in the severe ICP group when compared with the mild group (26,27), but conflicting results have been reported (29) in the literature. Also in our study, we didn't find an increased MSA risk in the severe group when compared with the mild group. Fetal asphyxia in the newborns of patients with ICP has been reported frequently in the literature (30,31). Overall, the characteristics of these patients show wide variations, and the findings are inconsistent in the literature (30).

Previous studies about ICP and inflammation suggested that ICP was an inflammatory process, and that perinatal outcomes were related to inflammation (18,31-33). Bile acids are thought to be related to inflammation, and they directly affect hepatocytes and stimulate the secretion of proinflammatory mediators, which causes neutrophil accumulation, extravasation, and activation (17). Prior studies used the hematologic markers WBC (18), MPV (31,32), and NLR (18) as inflammatory markers in ICP. However, as far as we know, no studies have investigated the relationships between ICP and PLR and RDW. Therefore, to the best of our knowledge, this paper is the first to determine the associations between ICP and all CBC inflammatory markers. The results showed that serum bile acids were positively and significantly correlated with PLR (r=0.343, p=0.003), and the ICP group had a significantly increased PLR and significantly decreased RDW ratio when compared with the controls. Despite the increased PLRs and decreased RDWs in the patients with ICP, they were not significantly changed in severe ICP. Kirbas et al. (18) found significantly higher mean WBC and NLR values and a lower lymphocyte count in their severe ICP group than in controls, and NLR was found to be even higher in patients with mild ICP. They also found a significant association between fasting TBA levels and NLR (18). However, we found that neutrophil and lymphocyte counts were significantly decreased in patients with ICP; NLRs were similar between the normal and ICP group. Platelets in the blood vary in size, with the granules and adhesion molecules of the platelets increasing when they become larger and play an active role in homeostasis (34). MPV, which is the most frequently used platelet size measurement, is also an index of platelet activation (34). Platelets release thrombin, which plays a role in inflammation (34) and angiogenesis (35), and a high platelet volume allows greater coagulability and fibrinolysis (36). However, there is a limited number of studies about the relationship between MPV and the severity of ICP, and the relationship between MPV and perinatal outcomes, even though an MPV increase can be seen in patients with ICP (31,32). Kebapcilar et al. (31) investigated the relationship between coagulation parameters and low 5-minute Apgar scores in both patients with ICP and normal pregnancies. In addition, Oztas et al. (32) reported higher MPVs in patients with ICP when compared with a control group, with an increased preterm delivery likelihood just after exceeding an MPV of 11.2 fL. In our study, MPV was significantly increased in women with ICP cases compared with healthy controls. Moreover, apart from the PLR and WBC, the MPV levels increased in the severe group.

Study Limitations

The main limitation of this study was its retrospective design, but despite this methodologic limitation, this research investigated all of the available hematologic inflammatory parameters. It confirmed prior data that inflammatory markers are significantly increased in patients with ICP. Despite the significant changes in the inflammatory markers in patients with ICP, only MPV was significantly increased with the severity of the disease. These results suggest that MPV may be a valuable marker in patients with severe ICP, but large scale studies are needed to confirm this result.

Conclusion

Based on the results of this study, the inflammatory markers were significantly increased in patients with ICP. PLR, WBC, and MPV were all significantly increased, whereas the RDW was significantly decreased in ICP. MPV was related to the severity of disease and might be a valuable marker for ICP disease severity in the future.

Ethics

Ethics Committee Approval: This study was approved by the Zeynep Kamil Women and Children's Health Training and Research Hospital Local Ethics Committee (approval number: 136).

Informed Consent: Consent form was filled out by all participants.

Peer-review: External and internal peer-reviewed.

Authorship Contributions

Surgical and Medical Practices: C.Y.A., F.V., O.P., C.K., Concept: C.Y.A., F.V., Design: C.Y.A., F.V., Data Collection or Processing: C.Y.A., E.B.E., I.Y., A.E., O.P., Analysis or Interpretation: C.Y.A., F.V., E.B.E., Literature Search: C.Y.A., I.Y., C.K., Writing: C.Y.A., F.V .

Conflict of Interest: No conflict of interest was declared by the authors.

Financial Disclosure: The authors declared that this study received no financial support.

References

(1.) Lammert F, Marschall HU, Glantz A, Matern S. Intrahepatic cholestasis of pregnancy: molecular pathogenesis, diagnosis and management. J Hepatol 2000;33:1012-21.

(2.) Arrese M, Reyes H. Intrahepatic cholestasis of pregnancy: a past and present riddle. Ann Hepatol 2006;5:202-5.

(3.) Pathak B, Sheibani L, Lee RH. Cholestasis of pregnancy. Obstet Gynecol Clin North Am 2010;37:269-82.

(4.) Heinonen S, Kirkinen P. Pregnancy outcome with intrahepatic cholestasis. Obstet Gynecol 1999;94:189-93.

(5.) Kenyon A P, Piercy CN, Girling J, Williamson C, Tribe RM, Shennan AH. Pruritus may precede abnormal liver function tests in pregnant women with obstetric cholestasis: a longitudinal analysis. BJOG 2001;108:1190-2.

(6.) Ropponen A, Sund R, Riikonen S, Ylikorkala O, Aittomaki K. Intrahepatic cholestasis of pregnancy as an indicator of liver and biliary diseases: a population-based study. Hepatology 2006;43:723-8.

(7.) Geenes V, Williamson C. Liver disease in pregnancy. Best Pract Res Clin Obstet Gynecol 2015;29:612-24.

(8.) Brouwers L, Koster M P, Page-Christiaens GC, Kemperman H, Boon J, Evers IM, et al. Intrahepatic cholestasis of pregnancy: maternal and fetal outcomes associated with elevated bile acid levels. Am J Obstet Gynecol 2015;212:100.e1-e7.

(9.) Geenes V, Williamson C. Intrahepatic cholestasis of pregnancy. World J Gastroenterol 2009;15:2049-66.

(10.) Diken Z, Usta IM, Nassar AH. A Clinical Approach to Intrahepatic Cholestasis of Pregnancy. Am J Perinatol 2014;31:1-8.

(11.) Geenes V, Chappell LC, Seed PT, Steer PJ, Knight M, Williamson C. Association of severe intrahepatic cholestasis of pregnancy with adverse pregnancy outcomes: a prospective population-based case-control study. Hepatology 2014;59:1482-91.

(12.) Rook M, Vargas J, Caughey A, Bacchetti P, Rosenthal P, Bull L. Fetal outcomes in pregnancies complicated by intrahepatic cholestasis of pregnancy in a Northern California cohort. PLoS One 2012;7:e28343.

(13.) Asulyman OM, Ouzounian JG, Ames-Castro M, Goodwin TM. Intrahepatic cholestasis of pregnancy: perinatal outcome associated with expectant management. Am j obstet Gynecol 1996;175:9957-60.

(14.) Oztekin D, Aydal I, Oztekin O, Okcu S, Borekci R, Tinar S. Predicting fetal aspyhxia in intrahepatic cholestasis of pregnancy. Arch Gynecol Obstet 2009;280:975-9.

(15.) Nunez J, Nunez E, Bodi V, Sanchis J, Minana G, Mainar L, et al. Usefulness of the neutrophil to lymphocyte ratio in predicting long-term mortality in ST segment elevation myocardial infarction. Am J Cardiol 2008;101:747-52.

(16.) Zhang W W, Liu KJ, Hu GL, Liang WJ. Preoperative platelet/lymphocyte ratio is a superior prognostic factor compared to other systemic inflammatory response markers in ovarian cancer patients. Tumour Biol 2015;36:8831-7.

(17.) Allen K, Jaeschke H, Copple BL. Bile acids induce inflammatory genes in hepatocytes: a novel mechanism of inflammation during obstructive cholestasis. Am J Pathol 2011;178:175-86.

(18.) Kirbas A, Biberoglu E, Daglar K, Iskender C, Erkaya S, Dede H, et al. Neutrophil-to-lymphocyte ratio as a diagnostic marker of intrahepatic cholestasis of pregnancy. Eur J Obstet Gynecol Reprod Biol 2014;180:12-5.

(19.) Garcia-Flores J, Canamares M, Cruceyra M, Garicano A, Espada M, Lopez A, et al. Clinical value of maternal bile Acid quantification in intrahepatic cholestasis of pregnancy as an adverse perinatal outcome predictor. Gynecol Obstet Invest 2015;79:222-8.

(20.) Glantz A, Marschall HU, Mattsson LA. Intrahepatic cholestasis of pregnancy: Relationships between bile acid levels and fetal complication rates. Hepatology 2004;40:467-74.

(21.) Roncaglia N, Arreghini A, Locatelli A, Bellini P, Andreotti C, Ghidini A. Obstetric cholestasis: outcome with active management. Eur J Obstet Gynecol Reprod Biol 2002;100:167-70.

(22.) Puljic A, Kim E, Page J, Esakoff T, Shaffer B, LaCoursiere DY, et al. The risk of infant and fetal death by each additional week of expectant management in intrahepatic cholestasis of pregnancy by gestational age. Am J Obstet Gynecol 2015;212:667.e1-5.

(23.) Kondrackiene J, Kupcinskas L. Intrahepatic cholestasis of pregnancy-current achievements and unsolved problems. World J Gastroenterol 2008;14:5781-8.

(24.) Kawakita T, Parikh LI, Ramsey PS, Huang CC, Zeymo A, Fernandez M, et al. Predictors of adverse neonatal outcomes in intrahepatic cholestasis of pregnancy. Am Obstet Gynecol 2015;213:570.e1-e8.

(25.) Friberg AK, Zingmark V, Lyndrup J. Early induction of labor in high-risk intrahepatic cholestasis of pregnancy: what are the costs? Arch Gynecol Obstet 2016;294:709-14.

(26.) Lee RH, Kwok KM, Ingles S, Wilson ML, Mullin P, Incerpi M, et al. Pregnancy outcomes during an era of aggressive management for intrahepatic cholestasis of pregnancy. Am J Perinatol 2008;25:341-5.

(27.) Wikstrom Shemer E, Marschall HU, Ludvigsson J, Stephansson O. Intrahepatic cholestasis of pregnancy and associated adverse pregnancy and fetal outcomes: a 12-year population-based cohort study. BJOG 2013;120:717-23.

(28.) Blackwell SC, Wolfe HM, Redman ME, Hassan SS, Berry SM, Treadwell MC, et al. Relationship between meconium staining and amniotic fluid volume in term pregnancies. Fetal Diagn Ther 2002;17:78-82.

(29.) Sargin Oruc A, Seckin B, Ozcan N, Ozyer S, Uzunlar O, Danisman N. Role of postprandial bile acids in prediction of perinatal outcome in intrahepatic cholestasis of pregnancy. J Obstet Gynaecol Res 2014;40:1883-9.

(30.) Sentilhes L, Verspyck E, Pia P, Marpeau L. Fetal death in a patient with intrahepatic cholestasis of pregnancy. Obstet Gynecol 2006;107:458-60.

(31.) Kebapcilar AG, Taner CE, Kebapcilar L, Bozkaya G. High mean platelet volume, low-grade systemic coagulation, and fibrinolytic activation are associated with pre-term delivery and low APGAR score in intrahepatic cholestasis of pregnancy. J Matern Fetal Neonatal Med 2010;23:1205-10.

(32.) Oztas E, Erkenekli K, Ozler S, Ersoy AO, Kurt M, Oztas E, et al. Can routine laboratory parameters predict uadverse pregnancy outcomes in intrahepatic cholestasis of pregnancy? J Perinat Med 2015;43:667-74.

(33.) Biberoglu E, Kirbas A, Daglar K, Kara O, Karabulut E, Yakut HI, et al. Role of inflammation in intrahepatic cholestasis of pregnancy. J Obstet Gynaecol Res 2016;42:252-7.

(34.) Martin J F, Trowbridge EA, Salmon G, Plumb J. The biological significance of platelet volume: its relationship to bleeding time, platelet thromboxane B2 production and megakaryocyte nuclear DNA concentration. Thromb Res 1983;32:443-60.

(35.) Kisucka J, Butterfield CE, Duda DG, Eichenberger SC, Saffaripour S, Ware J, et al. Platelets and platelet adhesion support angiogenesis while preventing excessive hemorrhage. Proc Natl Acad Sci U S A 2006;103:855-60.

(36.) Ross R. Atherosclerosis:an inflammatory disease. N Engl J Med 1999;340:115-26.

Cigdem Yayla Abide (1), Fisun Vural (2), Cetin Kilicci (1), Evrim Bostanci Ergen (1), Ilter Yenidede (1), Ahmet Eser (1), Oya Pekin (1)

(1) University of Health Sciences, Zeynep Kamil Women and Children's Health Training and Research Hospital, Clinic of Obstetrics and Gynecology, Istanbul, Turkey

(2) University of Health Sciences, Haydarpasa Numune Training and Research Hospital, Clinic of Obstetrics and Gynecology, Istanbul, Turkey

Address for Correspondence/Yazisma Adresi: Cigdem Yayla Abide, MD, University of Health Sciences, Zeynep Kamil Women and Children's Health Training and Research Hospital, Clinic of Obstetrics and Gynecology, Istanbul, Turkey

Phone: +90 506 601 56 00 E-mail: cigdemabide@gmail.com ORCID ID: orcid.org/0000-0001-5437-7987

Received/Gelis Tarihi: 27.05.2017 Accepted/Kabul Tarihi: 16.09.2017

[c]Copyright 2017 by Turkish Society of Obstetrics and Gynecology

Turkish Journal of Obstetrics and Gynecology published by Galenos Publishing House

DOI: 10.4274/tjod.67674
Table 1. The basal characteristics of mild (n=53) and severe (n=31)
intrahepatic cholestasis of pregnancy

                                       Mild ICP    Severe ICP

Age <35 years                          42 (79.2%)  22 (70.9%)
BMI (overweight/obese) (kg/[m.sup.2])  41 (77.3%)  23 (74.1%)
Nulliparity                            33 (62.5%)  11 (35.4%)
Abortion                               17 (32%)     8 (25.8%)
Education (primary school)             38 (71.6%)  26 (83.8%)
Prior ICP                               4 (7.5%)    2 (6.4%)
IVF pregnancy                           3 (5.8%)    2 (6.4%)
Progesterone use in pregnancy          13 (22.6%)   5 (16.1%)

ICP: Intrahepatic cholestasis of pregnancy, BMI: Body mass index, IVF:
In vitro fertilization

Table 2. The comparison of the laboratory findings between patients
with mild and severe intrahepatic cholestasis of pregnancy

                               Mild ICP          Severe ICP
                                (n=53)             (n=31)

Hemoglobin (g/dL)           11.1[+ or -]1.1     11.0[+ or -]1.1
Hematocrit (%)              34.0[+ or -]4.1     34.1[+ or -]3.0
Alkaline phosphatase       259[+ or -]391.2    249[+ or -]102.0
(ng/mL)
Lactate dehydrogenase       24.3[+ or -]71.0    25.0[+ or -]51.0
(U/L)
Gamaglutamyl transferase    27.7[+ or -]28.7    23.8[+ or -]14.5
(U/L)
AST (U/L)                  135.1[+ or -]139.2  144.8[+ or -]173.1
ALT (U/L)                  134.1[+ or -]133.5   94.3[+ or -]96.4
Bile acids ([micro]mol/L)   20.5[+ or -]7.6     78.9[+ or -]50.0
Fibrinogen (mg/dL)          54[+ or -]105.0     52.0[+ or -]128.0

                           p ([dagger])


Hemoglobin (g/dL)           0.757
Hematocrit (%)              0.895
Alkaline phosphatase        0.899
(ng/mL)
Lactate dehydrogenase       0.648
(U/L)
Gamaglutamyl transferase    0.518
(U/L)
AST (U/L)                   0.773
ALT (U/L)                   0.133
Bile acids ([micro]mol/L)  <0.001
Fibrinogen (mg/dL)          0.743

([dagger]) P value is obtained by t-test (Levene test used for
homogeneity of variances)
ICP: Intrahepatic cholestasis of pregnancy, AST: Aspartate
aminotransferase, ALT: Alanine aminotransferase

Table 3. The comparison of obstetric outcomes in mild (n=53) and severe
(n=31) intrahepatic cholestasis of pregnancy

Mean [+ or -] SD                      Mild ICP

Gestational age at diagnosis        (33.5[+ or -]2.8)
Gestational age at delivery         (36.7[+ or -]1.2)
Birth weight (g)                  (2975[+ or -]568)
Cesarean rate n (%)                  29 (54.7%)
n (%) Male fetus                     20 (37.7%)
Fetal distress                        2 (3.7%)
Low Apgar score                       1 (1.9%)
Meconium stained aminiotic fluid      2 (3.8%)
Perinatal mortality                   0 (0%)
Neonatal mortality                    1 (1.9%)
Neonatal intensive care unit         10 (19%)
Preeclampsia                          7 (13.2%)
Gestational diabetes                 13 (24.5%)
Rh isoimmunization                    8 (15%)
Hyperemesis gravidarum                1 (1.9%)
Abortus imminence                     7 (13.2%)

Mean [+ or -] SD                     Severe ICP

Gestational age at diagnosis        (30.8[+ or -]4.7) ([dagger])
Gestational age at delivery         (35.3[+ or -]3.2) ([dagger])
Birth weight (g)                  (2733[+ or -]653)
Cesarean rate n (%)                  26 (83.6%) ([dagger])
n (%) Male fetus                     11 (35.4%)
Fetal distress                        4 (12.9%)
Low Apgar score                       2 (6.4%)
Meconium stained aminiotic fluid      3 (9.6%)
Perinatal mortality                   1 (3.2%)
Neonatal mortality                    1 (3.2%)
Neonatal intensive care unit          9 (29%)
Preeclampsia                          2 (6.4%)
Gestational diabetes                  4 (12.9%)
Rh isoimmunization                    4 (12.9%)
Hyperemesis gravidarum                1 (3.2%)
Abortus imminence                     4 (12.9%)

P values were obtained using chi-square test or the t-test as
appropriate (([dagger]) significant at p<0.05 level)
ICP: Intrahepatic cholestasis of pregnancy, SD: Standard deviation

Table 4. The comparison of hematologic indices between control and
intrahepatic cholestasis of pregnancy group

Hematologic parameters                    ICP (n=84)


Hemoglobin (g/dL)                      11.0[+ or -]1.1
Hematocrit (%)                         34.1[+ or -]3.7
Platelet ([10.sup.3]/[mm.sup.3])      249[+ or -]80
White blood cell count              17449[+ or -]3932
([10.sup.3]/[mm.sup.3])
Neutrophil ([10.sup.3]/[mm.sup.3])      7.2[+ or -]2.2
Lymphocyte ([10.sup.3]/[mm.sup.3])      1.8[+ or -]0.5
MPV (f/L)                               9.2[+ or -]2.6
RDW (%)                                15.1[+ or -]2.7
NLR                                     4.1[+ or -]1.7
PLR                                   145[+ or -]64

Hematologic parameters                   Control        p ([dagger])
                                         (n=145)

Hemoglobin (g/dL)                      10.0[+ or -]1     0.11
Hematocrit (%)                         34.3[+ or -]3     0.66
Platelet ([10.sup.3]/[mm.sup.3])      246[+ or -]69      0.81
White blood cell count              10333[+ or -]2259   <0.001
([10.sup.3]/[mm.sup.3])
Neutrophil ([10.sup.3]/[mm.sup.3])      7.9[+ or -]1.9   0.04
Lymphocyte ([10.sup.3]/[mm.sup.3])      2.0[+ or -]0.5   0.01
MPV (f/L)                               8.2[+ or -]1.2   0.004
RDW (%)                                17.1[+ or -]3.4  <0.001
NLR                                     4.0[+ or -]1.4   0.77
PLR                                   125[+ or -]43      0.02

([dagger]) P value is obtained by t-test (Levene test used for
homogeneity of variances) ICP: Intrahepatic cholestasis of pregnancy,
MPV: Mean platelet volume, RDW: Red blood cell distribution width, NLR:
Neutrophil-to-lymphocyte ratio, PLR: Platelet-to-lymphocyte ratio

Table 5. The comparison of inflammatory markers

                            Control (n=145)      Mild ICP (n=53)

WBC ([10.sup.3]/[mm.sup.3]   10.360[+ or -]2300   15.000[+ or -]3670
Platelet
([10.sup.3]/[mm.sup.3])     246[+ or -]68.0      242[+ or -]72.3
MPV (f/L)                     8.2[+ or -]1.2       8.7[+ or -]1.9
RDW (%)                      17.1[+ or -]3.4      15.5[+ or -]2.6
NLR                           4.0[+ or -]1.4       4.3[+ or -]1.7
PLR                         125.4[+ or -]43.0    144.0[+ or -]61.0

                            Severe ICP (n=31)  p  ([dagger])

WBC ([10.sup.3]/[mm.sup.3]   21.4[+ or -]4419  <0.001
Platelet
([10.sup.3]/[mm.sup.3])     261[+ or -]93.6     0.525
MPV (f/L)                    10.1[+ or -]3.4   >0.001
RDW (%)                      14.3[+ or -]2.8   >0.001
NLR                           3.8[+ or -]1.5    0.312
PLR                         147.0[+ or -]69.0   0.06

([dagger]) P value is obtained by ANOVA test (post-hoc least
significant difference is used for subgroup analysis)
WBC: White blood cell count, MPV: Mean platelet volume, RDW: Red blood
cell distribution width, NLR: Neutrophil-to-lymphocyte ratio, PLR:
Platelet-to-lymphocyte ratio
COPYRIGHT 2017 Galenos Yayinevi Tic. Ltd.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Clinical Investigation / Arastirma
Author:Abide, Cigdem Yayla; Vural, Fisun; Kilicci, Cetin; Ergen, Evrim Bostanci; Yenidede, Ilter; Eser, Ahm
Publication:Turkish Journal of Obstetrics and Gynecology
Article Type:Report
Date:Sep 1, 2017
Words:4619
Previous Article:No increase in free fetal DNA level in ectopic pregnancy: A preliminary study/Ektopik gebelik tanisinda serbest fetal DNA'nin yeri: On hazirlik...
Next Article:Third trimester anemia extends the length of hospital stay after delivery/Ucuncu trimesterdeki anemi dogum sonrasi hastanede kalis suresini...
Topics:

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters