<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jin X</submitter><funding>Pfizer</funding><funding>Astra Zeneca</funding><funding>Bayer</funding><funding>NovoNordisk</funding><funding>Nestle</funding><funding>Merck Serono</funding><funding>Illuminatio Medical Technology</funding><funding>Zuellig Pharma</funding><funding>Abbott</funding><funding>Boehringer Ingelheim</funding><funding>HKSAR</funding><funding>Eli-Lilly</funding><funding>Dexcom</funding><funding>Kyowa Kirin</funding><funding>Sanofi</funding><funding>Gilead Sciences</funding><funding>Merck Sharp and Dohme</funding><pagination>353-367</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12835781</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(1)</volume><pubmed_abstract>&lt;h4>Background/aims&lt;/h4>Previous studies suggest that hypothyroidism is associated with metabolic dysfunction-associated steatotic liver disease (MASLD) and its histological severity, but clinical outcome data are largely lacking. We aimed to study the impact of hypothyroidism on liver-related events (LREs).&lt;h4>Methods&lt;/h4>Patients with MASLD were identified from a territory-wide registry in Hong Kong during 2000-2024. Thyroid status was determined using diagnosis codes and thyroid function tests. The primary outcome, LRE, was defined as a composite of hepatic decompensation, hepatocellular carcinoma, liver transplantation, and liver-related death.&lt;h4>Results&lt;/h4>A total of 20,478 patients with MASLD were included in the final analysis (mean age 56.4±13.2 years; 43.9% male). At baseline, 18,178 (88.8%) patients were euthyroid, 598 (2.9%) were hyperthyroid, and 1,702 (8.3%) were hypothyroid. Compared with euthyroid patients, both hyperthyroidism and overt hypothyroidism were associated with cirrhosis. At a median follow-up of 4.8 years, 179 patients developed LREs, and 26 died from liver disease. Compared with patients with normal serum thyroid-stimulating hormone (TSH) levels of 0.4-4 mIU/L, those with subclinical (4-10 mIU/L; adjusted time-dependent cause-specific hazard ratio [aCSHR], 2.49; 95% CI, 1.51-4.13) and overt hypothyroidism (>10 mIU/L; aCSHR, 4.91; 95% CI, 1.56-15.47) had an increased risk of LREs. Time-dependent, but not baseline, TSH and thyroid status were associated with LRE risk.&lt;h4>Conclusions&lt;/h4>Subclinical and overt hypothyroidism are associated with an increased risk of LREs in a dose-dependent manner. The association with time-dependent but not baseline thyroid status underscores the importance of thyroid monitoring and suggests that correction of hypothyroidism may mitigate LRE risk.</pubmed_abstract><journal>Clinical and molecular hepatology</journal><pubmed_title>Hypothyroidism and the risk of liver-related events in patients with metabolic dysfunction-associated steatotic liver disease.</pubmed_title><pmcid>PMC12835781</pmcid><funding_grant_id>14106923</funding_grant_id><pubmed_authors>Wong GL</pubmed_authors><pubmed_authors>Lai JC</pubmed_authors><pubmed_authors>Jin X</pubmed_authors><pubmed_authors>Wong VW</pubmed_authors><pubmed_authors>Yip TC</pubmed_authors><pubmed_authors>Kong AP</pubmed_authors><pubmed_authors>Xiao X</pubmed_authors><pubmed_authors>Peng N</pubmed_authors><pubmed_authors>Song SJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hypothyroidism and the risk of liver-related events in patients with metabolic dysfunction-associated steatotic liver disease.</name><description>&lt;h4>Background/aims&lt;/h4>Previous studies suggest that hypothyroidism is associated with metabolic dysfunction-associated steatotic liver disease (MASLD) and its histological severity, but clinical outcome data are largely lacking. We aimed to study the impact of hypothyroidism on liver-related events (LREs).&lt;h4>Methods&lt;/h4>Patients with MASLD were identified from a territory-wide registry in Hong Kong during 2000-2024. Thyroid status was determined using diagnosis codes and thyroid function tests. The primary outcome, LRE, was defined as a composite of hepatic decompensation, hepatocellular carcinoma, liver transplantation, and liver-related death.&lt;h4>Results&lt;/h4>A total of 20,478 patients with MASLD were included in the final analysis (mean age 56.4±13.2 years; 43.9% male). At baseline, 18,178 (88.8%) patients were euthyroid, 598 (2.9%) were hyperthyroid, and 1,702 (8.3%) were hypothyroid. Compared with euthyroid patients, both hyperthyroidism and overt hypothyroidism were associated with cirrhosis. At a median follow-up of 4.8 years, 179 patients developed LREs, and 26 died from liver disease. Compared with patients with normal serum thyroid-stimulating hormone (TSH) levels of 0.4-4 mIU/L, those with subclinical (4-10 mIU/L; adjusted time-dependent cause-specific hazard ratio [aCSHR], 2.49; 95% CI, 1.51-4.13) and overt hypothyroidism (>10 mIU/L; aCSHR, 4.91; 95% CI, 1.56-15.47) had an increased risk of LREs. Time-dependent, but not baseline, TSH and thyroid status were associated with LRE risk.&lt;h4>Conclusions&lt;/h4>Subclinical and overt hypothyroidism are associated with an increased risk of LREs in a dose-dependent manner. The association with time-dependent but not baseline thyroid status underscores the importance of thyroid monitoring and suggests that correction of hypothyroidism may mitigate LRE risk.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-15T04:56:49.135Z</modification><creation>2026-06-15T03:08:31.723Z</creation></dates><accession>S-EPMC12835781</accession><cross_references><pubmed>41321024</pubmed><doi>10.3350/cmh.2025.0860</doi></cross_references></HashMap>