Non-alcoholic fatty liver disease in pregnancy is associated with adverse maternal and perinatal outcomes.


Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
09 2020
Historique:
received: 23 11 2019
revised: 03 03 2020
accepted: 22 03 2020
pubmed: 13 6 2020
medline: 9 11 2021
entrez: 13 6 2020
Statut: ppublish

Résumé

The prevalence of non-alcoholic fatty liver disease (NAFLD) is rising in young adults, with potential implications for reproductive-aged women. Whether NAFLD during pregnancy confers more serious risks for maternal or perinatal health is unclear. Using weighted discharge data from the US national inpatient sample, we evaluated temporal trends of NAFLD in pregnancies after 20 weeks gestation, and compared outcomes to pregnancies with other chronic liver diseases (CLDs) or no CLD. Study outcomes included preterm birth, postpartum hemorrhage, hypertensive complications (pre-eclampsia, eclampsia, and/or hemolysis, elevated liver enzymes, and low platelets syndrome), and maternal or fetal death. NAFLD prevalence was estimated by calendar year and temporal trends tested by linear regression. Outcomes were analyzed by logistic regression adjusted for age, race, multiple gestation, and pre-pregnancy diabetes, obesity, dyslipidemia and hypertension. Among 18,574,225 pregnancies, 5,640 had NAFLD and 115,210 had other, non-NAFLD CLD. Pregnancies with NAFLD nearly tripled from 10.5/100,000 pregnancies in 2007 to 28.9/100,000 in 2015 (p <0.001). Compared to the other groups, patients with NAFLD during pregnancy more frequently experienced gestational diabetes (7-8% vs. 23%), hypertensive complications (4% vs. 16%), postpartum hemorrhage (3-5% vs. 6%), and preterm birth (5-7% vs. 9%), all p values ≤0.01. On adjusted analysis, compared to no CLD, NAFLD was associated with hypertensive complications, preterm birth, postpartum hemorrhage and possibly maternal (but not fetal) death. The prevalence of NAFLD in pregnancy has nearly tripled in the last decade and is independently associated with hypertensive complications, postpartum hemorrhage and preterm birth. NAFLD should be considered a high-risk obstetric condition, with clinical implications for pre-conception counseling and pregnancy care. The prevalence of non-alcoholic fatty liver disease (NAFLD) in pregnancy has almost tripled over the past 10 years. Having NAFLD during pregnancy increases risks for both the mother and the baby, including hypertensive complications of pregnancy, bleeding after delivery, and preterm birth. Thus, pre-conception counseling is warranted with consideration of high-risk obstetric management among women with NAFLD in pregnancy.

Sections du résumé

BACKGROUND & AIMS
The prevalence of non-alcoholic fatty liver disease (NAFLD) is rising in young adults, with potential implications for reproductive-aged women. Whether NAFLD during pregnancy confers more serious risks for maternal or perinatal health is unclear.
METHODS
Using weighted discharge data from the US national inpatient sample, we evaluated temporal trends of NAFLD in pregnancies after 20 weeks gestation, and compared outcomes to pregnancies with other chronic liver diseases (CLDs) or no CLD. Study outcomes included preterm birth, postpartum hemorrhage, hypertensive complications (pre-eclampsia, eclampsia, and/or hemolysis, elevated liver enzymes, and low platelets syndrome), and maternal or fetal death. NAFLD prevalence was estimated by calendar year and temporal trends tested by linear regression. Outcomes were analyzed by logistic regression adjusted for age, race, multiple gestation, and pre-pregnancy diabetes, obesity, dyslipidemia and hypertension.
RESULTS
Among 18,574,225 pregnancies, 5,640 had NAFLD and 115,210 had other, non-NAFLD CLD. Pregnancies with NAFLD nearly tripled from 10.5/100,000 pregnancies in 2007 to 28.9/100,000 in 2015 (p <0.001). Compared to the other groups, patients with NAFLD during pregnancy more frequently experienced gestational diabetes (7-8% vs. 23%), hypertensive complications (4% vs. 16%), postpartum hemorrhage (3-5% vs. 6%), and preterm birth (5-7% vs. 9%), all p values ≤0.01. On adjusted analysis, compared to no CLD, NAFLD was associated with hypertensive complications, preterm birth, postpartum hemorrhage and possibly maternal (but not fetal) death.
CONCLUSION
The prevalence of NAFLD in pregnancy has nearly tripled in the last decade and is independently associated with hypertensive complications, postpartum hemorrhage and preterm birth. NAFLD should be considered a high-risk obstetric condition, with clinical implications for pre-conception counseling and pregnancy care.
LAY SUMMARY
The prevalence of non-alcoholic fatty liver disease (NAFLD) in pregnancy has almost tripled over the past 10 years. Having NAFLD during pregnancy increases risks for both the mother and the baby, including hypertensive complications of pregnancy, bleeding after delivery, and preterm birth. Thus, pre-conception counseling is warranted with consideration of high-risk obstetric management among women with NAFLD in pregnancy.

Identifiants

pubmed: 32531415
pii: S0168-8278(20)30215-4
doi: 10.1016/j.jhep.2020.03.049
pmc: PMC7438303
mid: NIHMS1601598
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

516-522

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK111944
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK026743
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest MS is the site principal investigator for a NAFLD clinical trial funded by Zydus pharmaceuticals. NT is on the advisory board at Intercept Pharmaceuticals and receives grant support Gilead Sciences. No other authors have relevant conflicts of interest. Please refer to the accompanying ICMJE disclosure forms for further details.

Références

Am J Gastroenterol. 2016 May;111(5):658-64
pubmed: 27002796
Nat Rev Gastroenterol Hepatol. 2018 Jan;15(1):11-20
pubmed: 28930295
Hepatology. 2018 May;67(5):1726-1736
pubmed: 28941364
J Pediatr. 2013 May;162(5):930-6.e1
pubmed: 23260099
Liver Int. 2019 Apr;39(4):740-747
pubmed: 30179294
BJOG. 2017 Apr;124(5):e106-e149
pubmed: 27981719
Clin Liver Dis. 2016 May;20(2):325-38
pubmed: 27063272
JAMA. 2012 Feb 1;307(5):491-7
pubmed: 22253363
Diabetes. 1999 Apr;48(4):834-8
pubmed: 10102701
BJOG. 2017 Apr;124(5):804-813
pubmed: 27510598
Obstet Gynecol. 2017 Oct;130(4):e168-e186
pubmed: 28937571
J Pediatr Gastroenterol Nutr. 2015 Feb;60(2):152-8
pubmed: 25079479
Hepatology. 2018 Jan;67(1):108-122
pubmed: 28665032
Nat Rev Nephrol. 2019 May;15(5):275-289
pubmed: 30792480
Nat Rev Cardiol. 2018 Apr;15(4):230-240
pubmed: 29022571
Am J Public Health. 2010 Jun;100(6):1047-52
pubmed: 20395581
Liver Int. 2016 Feb;36(2):268-74
pubmed: 26114995
Clin Gastroenterol Hepatol. 2019 Mar;17(4):748-755.e3
pubmed: 29908364
J Obstet Gynaecol. 2013 May;33(4):331-7
pubmed: 23654309
PLoS One. 2019 Aug 26;14(8):e0221400
pubmed: 31449538
J Clin Gastroenterol. 2018 Apr;52(4):339-346
pubmed: 28961576
Hepatology. 2018 Jan;67(1):328-357
pubmed: 28714183
Nat Rev Dis Primers. 2019 Jul 11;5(1):47
pubmed: 31296866
Am J Gastroenterol. 2018 Nov;113(11):1649-1659
pubmed: 29880964
Am J Gastroenterol. 2016 May;111(5):665-70
pubmed: 26977755
Am J Clin Nutr. 2014 May;99(5):1034-40
pubmed: 24572562
JAMA. 2017 Nov 28;318(20):2011-2018
pubmed: 29183077
PLoS One. 2019 Apr 12;14(4):e0215326
pubmed: 30978266
Pediatr Res. 2011 Sep;70(3):287-91
pubmed: 21629154
Diabetologia. 2019 Feb;62(2):238-248
pubmed: 30470912
Cell Metab. 2008 Jun;7(6):496-507
pubmed: 18522831

Auteurs

Monika Sarkar (M)

Division of GI/Hepatology, University of California, San Francisco, San Francisco, CA, USA. Electronic address: monika.sarkar@ucsf.edu.

Joshua Grab (J)

Department of Surgery, University of California, San Francisco, San Francisco, CA, USA.

Jennifer L Dodge (JL)

Department of Surgery, University of California, San Francisco, San Francisco, CA, USA.

Erica P Gunderson (EP)

Kaiser Permanente Northern California, Division of Research, Oakland, CA, USA.

Jessica Rubin (J)

Division of GI/Hepatology, University of California, San Francisco, San Francisco, CA, USA.

Roxanna A Irani (RA)

Department of Obstetrics and Gynecology, University of California, San Francisco, San Francisco, CA, USA.

Marcelle Cedars (M)

Department of Obstetrics and Gynecology, University of California, San Francisco, San Francisco, CA, USA.

Norah Terrault (N)

Division of GI and Liver, University of Southern California, Los Angeles, CA, USA.

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Classifications MeSH