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Hepatol Int. 2026;20(1):69-80.

Metabolic dysfunction-associated steatotic liver disease and adverse pregnancy outcomes: a nationwide cohort study.

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제1저자 정영미 · 교신저자 김원, 조금준

소속 (8)
  1. Department of Obstetrics and Gynecology, Korea University College of Medicine, Seoul, Korea.
  2. Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Korea.
  3. Department of Statistics, Sungkyunkwan University, Seoul, Korea.
  4. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
  5. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea.
  6. Department of Obstetrics and Gynecology, Korea University College of Medicine, Seoul, Korea. md_cho@hanmail.net.
  7. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea. drwon1@snu.ac.kr.
  8. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea. drwon1@snu.ac.kr.

Abstract

PURPOSE A recent international consensus introduced revised nomenclature for steatotic liver disease (SLD). This study evaluated the impact of SLD subtypes on adverse pregnancy outcomes (apos) using updated criteria.

METHODS In this nationwide, population-based study, we analyzed 290,527 female who underwent health check-ups within 1 year before pregnancy and delivered singleton infants. Participants were categorized into non-SLD, metabolic dysfunction-associated steatotic liver disease (MASLD), metabolic dysfunction and alcohol-related liver disease (MetALD), and alcohol-related liver disease (ALD) groups.

RESULTS A total of 290,527 female were analyzed. Compared to female without SLD, those with MASLD (adjusted odds ratio [aOR] 2.44, 95% CI 2.33-2.55), MetALD (aOR 2.45, 95% CI 2.26-2.66) and ALD (aOR 2.28, 95% CI 2.11-2.47) had significantly higher risks of apos. These associations were observed for gestational diabetes mellitus (GDM), hypertensive disorders of pregnancy (HDP), and preterm birth. Both MASLD and ALD were associated with increased risk of low birthweight (aOR 1.15, 95% CI 1.05-1.27 and aOR 1.21, 95% CI 1.02-1.43, respectively), whereas MetALD was not (aOR 0.96, 95% CI 0.79-1.18). Due to the low incidence of placental abruption across all groups (0.3-0.5%), associations with this outcome remained inconclusive. Additionally, a higher number of cardiometabolic risk factors (CMRFs) was associated with an increased risk of apos (p for trend of odds < 0.0001).

CONCLUSION MASLD, MetALD, and ALD were independently associated with increased risks of apos, with risk further amplified by a greater number of CMRFs. These findings underscore the importance of enhanced prenatal management for female with pre-existing SLD, particularly those with multiple CMRFs, to mitigate the risk of apos.

© 2025. Asian Pacific Association for the Study of the Liver.

Keywords

Cardiometabolic risk factorsDiabetesGestationalHypertensionLiver diseasePregnancy outcomePregnancy-induced

Comment · 정정

Conflict of interest statement

Declarations. Conflict of interest: None to declare. Ethical approval: This study was conducted in accordance with the Declaration of Helsinki and was approved by the Institutional Review Board of Korea University Guro Hospital (IRB approval number: 2025GR0092). Due to the retrospective nature of this study and the use of de-identified patient data, the requirement for informed consent was waived by the ethics committee. This study used de-identified retrospective data, and no individual patient data that could lead to identification is presented.

그 밖의 정보
출판 형태
Journal Article
저널
Hepatology international · eISSN 1936-0541
전자 출판
2025-11-27
MeSH
Humans · Female · Pregnancy · Adult · Pregnancy Outcome* / epidemiology · Fatty Liver* / complications / epidemiology · Pregnancy Complications* / epidemiology · Diabetes, Gestational / epidemiology · Cohort Studies · Infant, Newborn · Premature Birth / epidemiology · Risk Factors · Hypertension, Pregnancy-Induced / epidemiology
연구비
National Research Foundation of Korea RS-2024-00427361 · National Research Foundation of Korea 2021R1A2C2005820 · National Research Foundation of Korea RS-2021-NR056442 · National Research Foundation of Korea RS-2022-NR067269 · National Research Foundation of Korea RS-2023-00223831 · National Research Foundation of Korea RS-2024-00440883
참고문헌
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