Total Alanine Aminotransferase (ALT) Flares in Pregnant North American Women With Chronic Hepatitis B Infection: Results From a Prospective Observational Study.


Journal

The American journal of gastroenterology
ISSN: 1572-0241
Titre abrégé: Am J Gastroenterol
Pays: United States
ID NLM: 0421030

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 15 5 2019
medline: 19 3 2020
entrez: 15 5 2019
Statut: ppublish

Résumé

Alterations in the immune system can result in alanine aminotransferase (ALT) flares either during pregnancy or after delivery in women with chronic hepatitis B virus (HBV) infection. The aim of this study was to prospectively assess changes in serum biochemical and virological markers of HBV infection during and after pregnancy in a large North American cohort of pregnant women with chronic HBV. Adult pregnant women enrolled in the Hepatitis B Research Network between 2011 and 2016 were included. Serum ALT values and HBV DNA viral levels were obtained at <28 weeks and >28 weeks of gestation and <16 weeks, 16-31 weeks, and 32-48 weeks postpartum. Outcomes of ALT flares included severity, duration, and initiation of antiviral therapy. Among the 158 pregnant women with chronic HBV, the median age was 33 years, 73% were Asian, and 63% were hepatitis B e antigen (HBeAg) negative. The median HBV DNA level was substantially higher in the HBeAg-positive vs HBeAg-negative women (1.3 × 10 vs 343 IU/mL), but serum ALT levels at their first study visit were similar. Among untreated pregnant women, there was a very mild increase in serum ALT postpartum among both HBeAg-positive and HBeAg-negative women (P < 0.001). Serum ALT flares (range 107-513 U/L) developed in 3.4% (5/149) during pregnancy and in 4.3% (4/92) after delivery. Twenty-two percent were initiated on antiviral therapy. After withdrawal of prophylactic anti-HBV therapy, 17.2% (5/29) developed serum ALT flares (range 107-208 U/L) within 14 weeks of drug discontinuation, and 3 additional women had flares despite continuous anti-HBV therapy during pregnancy or postpartum. Many ALT flares were not associated with significant changes in HBV DNA levels. No flares were severe with elevations of bilirubin or clinical decompensation. Spontaneous ALT flares in untreated pregnant women with chronic HBV are infrequent, mild, and self-limited both prepartum and postpartum. Although flares after the withdrawal of antiviral therapy postpartum are more common, they were also mild and self-limited. Further studies of the immunopathogenesis of pregnancy-related flares are needed, as well as effects on long-term outcome of the mother and infant.

Identifiants

pubmed: 31082876
doi: 10.14309/ajg.0000000000000221
pmc: PMC7132838
mid: NIHMS1564031
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
Hepatitis B e Antigens 0
Lamivudine 2T8Q726O95
Tenofovir 99YXE507IL
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1283-1291

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001111
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082923
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000058
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082867
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082874
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024986
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082919
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082927
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082872
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082943
Pays : United States
Organisme : NIAAA NIH HHS
ID : K24 AA022523
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK050306
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR000040
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082871
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082944
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082864
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082843
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082863
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000004
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK082866
Pays : United States

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Auteurs

Natalie H Bzowej (NH)

Ochsner Medical Center, New Orleans, Louisiana, USA.

Tram T Tran (TT)

Cedar Sinai Medical Center, Los Angeles, California, USA.

Ruosha Li (R)

University of Texas Health Science Center, Houston, Texas, USA.

Steven H Belle (SH)

University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Coleman I Smith (CI)

Georgetown University Hospital, Washington, District of Columbia, USA.

Mandana Khalili (M)

University of California San Francisco, San Francisco, California, USA.

Ray Chung (R)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Naoky Tsai (N)

University of Hawaii, Honolulu, Hawaii.

Norah Terrault (N)

University of California, San Francisco, San Francisco, California, USA.

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Classifications MeSH