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ISSN 2155-6113
Journal of AIDS & Clinical Research
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Intrahepatic Cholestasis of Pregnancy and Serum Bile Acids in HIV Infected Pregnant Women

Adriana Weinberg MD1,2,3,6,7*, Amanda Allshouse MS4,7, Kay Kinzie NP1,7, Alice Cho BS1, Jill K Davies MD5,6,8 and Elizabeth J Mc Farland MD1,7

1Department of Pediatrics, the University of Colorado School of Medicine, USA

2Department of Medicine, the University of Colorado School of Medicine, USA

3Department of Pathology, the University of Colorado School of Medicine, USA

4Department of Preventative Medicine, the University of Colorado School of Medicine, USA

5Departments of Obstetrics and Gynecology, the University of Colorado School of Medicine, USA

6University of Colorado Hospital, USA

7Childrens Hospital Colorado, Aurora CO, USA

8Denver Health Medical Center, Denver CO, USA

*Corresponding Author:
Adriana Weinberg
Professor of Pediatrics, Medicine and Pathology
University of Colorado Denver
12700 E. 19th Avenue, Aurora, CO 80045, USA
Tel: 3037244480
E-mail: [email protected]

Received date: May 20, 2015; Accepted date: May 22, 2015; Published date: May 30, 2015

Citation: Adriana Weinberg MD, Amanda Allshouse MS, Kay Kinzie NP, Alice Cho BS, Jill K Davies MD, et al. (2015) Intrahepatic Cholestasis of Pregnancy and Serum Bile Acids in HIV-Infected Pregnant Women. J AIDS Clin Res 6:464. doi:10.4172/2155-6113.1000464

Copyright: © 2015 Adriana Weinberg MD, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Objectives: Intra-hepatic cholestasis of pregnancy (ICP) is uncommon, but has severe effects on pregnancy outcomes. ICP is characterized by elevated serum bile acids and liver enzymes and preferentially affects women with liver disorders. We compared bile acids and pregnancy outcomes of HIV-infected pregnant women, who commonly have elevated live enzymes, with uninfected controls.

Methods: Twenty-four HIV-infected, including 2 co-infected with hepatitis C virus (HCV), and 25 uninfected women were tested during early and late pregnancy and postpartum.

Results: After exclusion of the HCV-infected women, serum bile acids were similar in HIV-infected and uninfected participants. -glutamyl transpeptidase was elevated in HIV-infected compared with uninfected women during pregnancy and postpartum. Bilirubin and aspartate transaminase were higher in uninfected compared with HIV-infected women in early pregnancy, but subsequently similar. Bile acids in late pregnancy correlated with bile acids in the baby at birth. An HIV- and HCV-co-infected pregnant woman with active hepatitis developed ICP complicated by fetal distress. Another co-infected participant without active hepatitis had an uneventful pregnancy and delivery.

Conclusion: In the absence of HCV co-infection, bile acid metabolism appeared to be similar in HIV-infected and uninfected pregnant women. Both HIV-infected and uninfected pregnant women had mild liver enzyme elevations.

Keywords

Intrahepatic cholestasis; Pregnancy; Human Immunodeficiency Virus; Antiretroviral Therapy; Hepatitis C virus; Bile acids; Liver function

Introduction

Intra-hepatic cholestasis of pregnancy (ICP) is a clinical complication of pregnancy defined by pruritus without rash occasionally accompanied by jaundice and elevated liver enzymes. It typically arises in the second half of pregnancy and subsides after delivery. Although this disease is distressing to the gravida, it has minimal long-term effects on maternal health, but carries significant risks to the fetus including prematurity, low birth weight, intrapartum asphyxia [1] and increased fetal mortality. ICP is associated with a 1-60% risk of fetal demise [2].

Biochemically, ICP is characterized by increased levels of serum bile acids sometimes in association with elevated liver enzymes, consistent with a pathogenic mechanism of decreased hepatic excretion of bile acids [3,4]. Bile acids may increase 10 to 100 fold over normal levels [5,6]. The retained bile acids are purported to have a vaso-constrictive effect on the fetal blood circulation leading to the serious complications mentioned above [7]. ICP may cause placental alterations that reduce the ability of the fetus to dispose of bile acids, as evidenced by elevated bile acids in cord blood and meconium [8]. There is no universally accepted treatment of ICP. Diphenhydramine or other symptomatic medication has been used to control pruritus and cholestyramine or ursodeoxycholic acid (UDCA) have been recommended to increase intestinal excretion and decrease reabsorption of bile acids [9]. UDCA has been proposed as a therapeutic intervention, because it decreases serum bile acid levels, improves maternal symptoms of ICP, and may decrease the incidence of fetal adverse events [10,11]. Elective early term delivery is also suggested, because most of the fetal mortality associated with ICP condition occurs after week 37 [12].

The decreased hepatic excretion of bile acids, which represents the pathogenic mechanism of ICP, has been ascribed to hepatic effects of estrogen and progesterone metabolites, which are typically elevated in pregnancy [3,4]. Genetic and nutritional factors [13,14] and liver injury also play a role in this disease. As such, the incidence of ICP varies from 0.1%-0.2% in Europe and North America to 12%-22% in areas of South Asia and South Americ10a and first degree relatives of affected women have a 20-fold higher risk [7,15]. HCV infection is associated with a 10-fold increase in the incidence of ICP over local background [16]; and elevated liver enzymes and/or total bilirubin are found in 30 to 50% of ICP cases [10,15].

HIV-infected pregnant women are subject to multiple hepatotoxic factors, which might affect their bile acid metabolism and increase their risk to develop ICP. Protease inhibitors (PI) commonly used for HIV therapy alter cytochrome P450 function, which is essential for normal enzymatic activity of the liver [17,18]. Some of the nucleoside (NRTI) and non-nucleoside analogue reverse transcriptase inhibitors (NNRTI) also have hepatotoxic effects by different mechanisms [18]. Antiretroviral (ARV)-associated hepatotoxicity is particularly common in pregnant women [19]. HIV infection per se has been associated with hepatitis, particularly in advanced stages of the disease, and with fatty liver. In addition, the epidemiology of HIV infection makes HCV infection, alcohol abuse, and other drug use more common in these patients than in the general population, further contributing to the overall decreased liver reserve in HIV-infected individuals [20]. Data regarding ICP and pregnancies complicated by HIV infection is scarce. ICP is passively reported to the Antiretroviral Pregnancy Registry (), but bile acid metabolism has not been systematically studied in HIVinfected pregnant women.

To explore if HIV infection and its therapy may be associated with abnormal bile acid metabolism, we conducted a pilot study comparing serum bile acid levels of HIV-infected pregnant women and their infants with those of HIV-uninfected mother-infant dyads.

Materials and Methods

Participants

The study was approved by the Colorado Multiple Institutions Review Board. HIV-infected and uninfected pregnant women who consented to this study were enrolled between the years of 2005 and 2009. Exclusion criteria were acute hepatitis, liver failure, preeclampsia with liver dysfunction and severe systemic illness.

Design

Participants underwent an ICP-targeted questionnaire and physical exam and had bile acids, alanine transaminase (ALT), aspartate transaminase (AST), γ-glutamyl transpeptidase (GGT) and total bilirubin were measured at entry, during 2nd trimester and/or 3rd trimester if different from entry and 6 to 12 weeks after delivery. A standardized meal was administered 2 hours before each set of tests. Assays were performed in CLIA- and CAP-certified clinical laboratories using FDA-approved methods. Reference normal values were as established by Abbassi-Ghavanati et al. [21]. For HIV-infected pregnant women, CD4 cell numbers, plasma HIV RNA and antiretroviral information were abstracted from medical records. Concomitant medications were recorded both in HIV-infected and uninfected participants. Cord blood was collected for bile acid measurements. Newborn physical exam information was abstracted from the medical records.

Statistical analyses

Demographics, clinical characteristics at study entry and laboratory values at each time point were summarized and compared between HIV-negative and HIV-positive groups using two-sample t-tests for continuous measures and chi-square tests for categorical measures. Scatterplots and Spearman’s Correlation were used to assess the monotonic relationship between fold-difference from threshold AST, ALT, and GGT with bile acids.

Results

Demographic and HIV disease characteristics at entry

The study enrolled 24 HIV-infected and 25 uninfected pregnant women. An HIV-infected woman withdrew from the study after the first visit and was excluded from the analysis. Two of the HIV-infected women had anti-HCV antibodies and were analyzed separately, because they had an established ICP risk factor. Table 1 summarizes the baseline characteristics of the remaining 46 subjects. There were no significant differences with respect to age, but there was an excess of black women in the HIV-infected compared with uninfected group. The parity was also significantly higher in HIV-infected compared with uninfected women. At entry, the 21 HIV-mono-infected participants were on highly active antiretroviral therapy (HAART) including 2 NRTIs in all subjects plus PIs (protease inhibitor or principal investigator?) in 19 subjects and NNRTIs in another 2 subjects. The most commonly used PI was lopinavir co-formulated with ritonavir (N=11) followed by atazanavir with ritonavir boost (N=5) and nelfinavir (N=3). The plasma HIV RNA was undetectable (<50 copies/mL) in 14 participants (70%); six participants had mean (95% CI) log10 plasma HIV RNA 2.87 (1.86, 3.89); and one participant did not have the data recorded. The mean (95% CI) CD4 count was 609 (490; 728) cells/μL.

  HIV positive
(n= 21)
HIV negative
(n=25)
p value
Mean age years (95% CI) 28.2 (24.91, 31.49) 30.4 (28.15, 32.72) 0.247
Mean week gestation (95% CI) 25.9 (22.78, 29.03) 19.9 (18.52, 21.29) 0.001
Ethnicity      
  Non- Hispanic 10 (47%) 19 (76%) 0.259
  Hispanic 5 (23%) 4 (16%)  
  Unknown 6 (29%) 2 (8%)  
Race      
  Not White 8 (38%) 0 <.001
  White 7 (33%) 23 (88%)  
  Unknown 6 (29%) 2 (8%)  
Parity      
  Nulliparous 6(29%) 23(88%) <.001
 Multiparous 7(33%) 1(4%)  
  Unknown 8 (38%) 1(4%)  
HAART      
  Yes 21 (100%)    
HIV plasma RNA      
<50 copies/mL 14 (67%)    
≥50 copies/mL 6 (29%)    
  Unknown 1 (4%)    
Mean Log10 Viral Load if not suppressed (95% CI) 2.87 (1.86, 3.89)    
Mean CD4 cells/mm3 (95% CI) 609 (490, 728)    

Table 1: Entry Demographic and HIV Disease Characteristics.

Bile acids and liver function tests (LFT) in HIV-infected and uninfected pregnant women

At entry [median (IQR) of 21.4 (19.5-24.5) weeks gestation], 7 of 20 HIV-infected and 10 of 23 uninfected pregnant women with available data had bile acid levels above the upper normal limit of the test for their gestational ages (Table 2). The geometric means of the serum bile acid concentrations did not differ significantly between the 2 groups. The highest level was observed in an HIV-infected subject at 23 μmol/L. At the last visit before delivery [median (IQR) of 36.0 (33.0-37.0) weeks gestation], 2 each HIV-infected and uninfected women had elevated bile acid levels for their gestational ages and the geometric means were also similar in the two groups. The highest bile acid level in late pregnancy of 22 μmol/L was observed in an uninfected asymptomatic woman. In the postpartum period [median (IQR) of 7.4 (5.6-12.1) weeks after delivery], 6 HIV-infected and 11 uninfected women had bile acid levels above the upper normal of non-pregnant women. Overall, only 1 HIVinfected and 1 uninfected woman had elevated bile acid levels at ≥ 2 visits.

  Geometric mean value (95% Confidence Interval) Number above upper limit of normal/number evaluated (%) p value
HIV positive HIV negative p value HIV positive HIV negative
Bile acids (μmol/L)
Entry1 4.96
(3.63, 6.76)
4.75
(4.05, 5.56)
0.798 7/20
(35.00)
10/23
(43.48)
0.571
Last pregnancy visit2 4.04
(3.43, 4.76)
4.45
(3.49, 5.68)
0.494 2/21
(9.52)
2/21
(9.52)
1.0
Post-partum3 4.73
(3.40, 6.59)
5.16
(4.18, 6.38)
0.639 6/14
(42.86)
11/18
(61.11)
0.305
Aspartatetransaminase (AST; U/L)
Entry 16.2
(12.85, 20.42)
22.5
(20.07, 25.13)
0.013 2/20
(10.00)
6/22
(27.27)
0.155
Last pregnancy visit 20.4
(15.93, 26.18)
24.0
(22.38, 25.76)
0.202 3/19
(15.79)
1/21
(4.76)
0.246
Post-partum 23.7
(17.26, 32.47)
27.7
(23.11, 33.26)
0.362 2/14
(14.29)
4/17
(23.53)
0.517
Alanine transaminase (ALT; U/L)
Entry 19.5
(14.57, 26.07)
19.6
(16.27, 23.65)
0.968 4/20
(20.00)
2/22
(9.09)
0.313
Last pregnancy visit 22.0
(16.38, 29.50)
18.0
(15.40, 20.95)
0.213 4/19
(21.05)
1/21
(4.76)
0.12
Post-partum 30.9
(22.81, 41.75)
29.5
(21.83, 39.81)
0.82 4/14
(28.57)
4/17
(23.53)
0.75
γ-glutamiltranspeptidase(GGT; U/L)
Entry 15.7
(8.03, 30.73)
11.0
(9.66, 12.47)
0.284 4/19
(21.05)
0/22
(0.00)
0.023
Last pregnancy visit 17.0
(7.80, 36.85)
10.8
(8.66, 13.55)
0.255 6/17
(35.29)
1/20
(5.00)
0.019
Post-partum 23.3
(13.67, 39.77)
13.2
(10.99, 15.79)
0.044 1/11
(9.09%)
0/17
(0.00)
0.206
Total bilirubin (mg/dL)
Entry 0.3
(0.24, 0.55)
0.59
(0.48, 0.72)
0.041 3/20
(15.00)
16/22
(72.73)
<0.001
Last pregnancy visit 0.42
(0.29, 0.62)
0.61
(0.51, 0.73)
0.077 2/19
(10.53)
7/21
(33.33)
0.085
Post-partum 0.56
(0.36, 0.88)
0.71
(0.57, 0.89)
0.321 1/13
(7.69)
0/17
(0.00)
0.245

Table 2: Maternal bile acids and liver function values during pregnancy and post-partum.

The proportions of HIV-infected and uninfected participants with elevated AST for gestational age did not differ significantly. AST concentrations were significantly lower at entry in HIV-infected compared with uninfected women (p=0.01), but concentrations were similar at subsequent visits. ALT levels were similar and the proportions of subjects with elevated levels for the gestational age were also similar in the 2 groups both in pregnancy and post-partum. GGT elevations were present in a higher proportion of HIV-infected compared with uninfected women, but all concentrations were < 3-fold of the upper normal level the test. Total bilirubin levels were high in 1 to 3 HIVinfected and 0 to 16 uninfected pregnant women across all time points, with concentrations < 3-fold of the upper normal level the test.

There was a weak, but significant correlation of bile acid with AST concentrations (ρ=0.37, p=0.02), but not with other LFTs (Figure 1).

aids-clinical-research-spearman

Figure 1: Correlation analyses of maternal serum bile acid and liver enzyme levels during late pregnancy. Data were derived from 43 pregnant women. Panels A, B and C show correlation analyses of bile acid levels with AST, ALT and GGT levels, respectively. Spearman coefficients of correlation and p values are shown on each graph.

Characteristics of the neonates and their bile acid levels

There were 47 newborns, including 45 singletons and 1 pair of twins, after exclusion of pregnancies complicated by HCV co-infection. Seven of 22 HIV-exposed infants with known gestational age at birth (31.8%) were born before 37 weeks gestation compared with 2 out of 23 unexposed (8.7%, p=0.05; Table 3). The birth weight was lower in HIVexposed compared with unexposed infants, but Apgar scores and bile acid levels were similar in HIV-exposed and unexposed infants.

  HIV exposed HIV unexposed p value
Mean weeks gestation at birth (95% CI) 38(36.9, 39.1) 39.1(38.3, 40) 0.099
Number born at <37 weeks gestation (percent) 7/22 (31.8) 2/23 (8.7) 0.053
Mean birth grams (95% CI) 2761 (2534, 2988) 3302 (3032, 3572) 0.003
 
Weight for gestational age
Number large for gestational age  (%) 0/21 (0) 5/22(22.7) 0.02
Number appropriate for gestational age (%)  21/21(100) 17/22 (77.3)  
 
Mean one-minute APGAR score (95% CI) 7.39 (6.45, 8.33) 7.59 (6.98, 8.2) 0.706
Mean five-minute APGAR score (95% CI) 8.78 (8.51, 9.05) 8.95 (8.79, 9.12) 0.254
Mean bile acids (μmol/mL; 95% CI) 4.45 (3.62, 5.45) 4.36 (3.30, 5.77) 0.961

Table 3: Infant characteristics at birth.

The analysis showed that late pregnancy maternal and infant cord blood bile acid concentrations had a correlation coefficient of 0.38 corresponding to a strong statistical trend (p=0.06; Figure 2). There were no significant correlations between maternal bile acid levels during late pregnancy and gestational age at delivery, infant weight or Apgar scores.

aids-clinical-research-association

Figure 2: Association of late pregnancy maternal and infant cord blood bile acid levels. Data were derived from 25 mother-infant pairs. The levels tended to correlate (rho=0.38, p=0.059) .

Pregnancies complicated by HIV and HCV co-infection

Two HIV and HCV co-infected pregnant women were enrolled. One of the women had HCV viremia in addition to antibodies against HCV. Her 3rd trimester bile acid concentration was approximately 11- fold the upper normal limit at 106 μmol/L. She also had elevated AST, ALT and GGT at 3-, 1.5- and 2-fold, respectively, the upper normal limit but normal total bilirubin. This participant did not develop pruritus, but had premature labor at 28 weeks gestation, fetal distress and meconium-stained amniotic fluid at delivery, which are wellrecognized complications of ICP. At the postpartum visit, the bile acid levels normalized at 8 μmol/L, but the hepatic enzymes remained elevated. The other HCV seropositive participant, who did not have detectable viremia, had an uneventful pregnancy and delivery and normal chemistry results at all visits.

Discussion

At the Children’s Immunodeficiency Mother-to-Child Prevention Program in Denver, Colorado, 4 out of 350 HIV-infected pregnant women were diagnosed with ICP over a period of 15 years, only 2 of whom had HCV co-infection (A. Weinberg, personal communication). One of these cases was complicated by fetal demise, which was avoided in the remaining 3 cases by early delivery with or without UDCA. This incidence of 1.14% was significantly higher compared with the overall incidence of 0.2% at our institution over a period of 5 years (26 cases of ICP per 13700 live births; J. Davies, personal communication) and prompted us to conduct this pilot study. However, our data showed that HIV infection and use of HAART during pregnancy were not associated with increased bile acid concentrations in the absence of HCV co-infection. The number of subjects enrolled in this study was too small to draw definitive conclusions on the incidence of ICP, but all the bile acid levels in pregnant women without HCV infection were <40 μmol/L, a threshold that has been previously shown to correlate with the development of ICP [22]. Therefore, our findings suggest that HIVinfected pregnant women on HAART may not be at increased risk of ICP in the absence of HCV co-infection. This is also in accordance with the Antiretroviral Pregnancy Registry data in which the incidence of ICP in HIV-infected pregnant women has been similar to the incidence in the general population.

Our data showed that GGT was more frequently abnormal in HIV-infected compared with uninfected pregnant women. Mildly elevated LFTs (<3-fold the upper normal level of the test) are common findings in HIV-infected individuals, including pregnant women, and may be caused by HIV-infection and/or drug-associated liver toxicity. However, mildly elevated occurred in a large proportion of HIVuninfected pregnant women, too. The frequency of mildly abnormal results was partially driven by the low pregnancy-specific normal standard values reported by Abbassi-Ghavanati et al. [21]. Correlation analyses showed significant associations between bile acid levels and AST concentrations, which did not differ between HIV-infected and uninfected pregnant women.

Very little is known about the effect of elevated serum bile acid levels in the fetus or infant other than the deleterious effect of highly increased serum bile acids on the overall outcome of pregnancy including increased incidence of spontaneous premature delivery, stained meconium, in-utero fetal distress and fetal demise. Fetal demise has been ascribed to vasoconstriction of the placental circulation [1]. We sought to determine if bile acid elevations below the threshold associated with ICP may be associated with placental deficiency reflected on infant gestational age and/or weight at birth and/or Apgar scores. Although none of the infant parameters measured in this study were associated with maternal bile acid levels in late pregnancy, the findings cannot be considered definitive due to the limited number of subjects with abnormal bile acid levels and the small elevations that were observed. Larger studies are warranted to further explore this association.

The HIV-infected pregnant woman with active HCV infection had high serum bile acids, in the range associated with ICP. Although she did not have pruritus, she had other complications consistent with ICP, including premature labor at 28 weeks gestation, fetal distress and meconium-stained amniotic fluid. This underscores the risk of ICP associated with active HCV infection. HCV co-infection occurs in 15 to 30% of HIV-infected individuals in the US [23]. HIV-infected pregnant women with active HCV infection may warrant serum bile acid level monitoring in the second half of pregnancy. The pregnancy outcome of women with bile acid concentrations ≥ 40 μmol/L, even in the absence of pruritus, may benefit from antepartum surveillance of the fetus beginning at 36 or 37 weeks gestation [22,24] or even as early as 26 to 27 weeks gestation in those women with known elevated levels or other risk factors for adverse outcome. In addition, new therapeutic interventions, such as dexamethasone, are being explored [25]. The results of a randomized trial of UCDA and/or induction of delivery at 37-38 weeks gestation may soon become available and may inform on the utility of these potential interventions [11].

Acknowledgements

This work was supported by grant M01 RR000069 (AW) and NIH/NCATS Colorado CTSI Grant Number UL1 TR000154. Contents are the authors’ sole responsibility and do not necessarily represent official NIH views. We thank Donna Roden for subject enrollment.

Conflicts of Interest

The authors do not have any conflicts of interest.

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