Lin Tiffany Y, Shekar Anshula O, Li Ning, Yeh Michael W, Saab Sammy, Wilson Mark, Leung Angela M
UCLA David Geffen School of Medicine, Los Angeles, CA, USA.
Department of Medicine, UCLA David Geffen School of Medicine, Los Angeles, CA, USA.
Clin Endocrinol (Oxf). 2017 May;86(5):755-759. doi: 10.1111/cen.13312. Epub 2017 Mar 9.
Abnormal serum liver function tests are common in patients with untreated thyrotoxicosis, even prior to the initiation of antithyroidal medications that may worsen the severity of the abnormal serum liver biochemistries. There is a wide range of the incidence of these abnormalities in the published literature. The aim of this study was to assess the risks factors and threshold of thyrotoxicosis severity for developing an abnormal liver biochemical test upon the diagnosis of new thyrotoxicosis.
Single-institution retrospective cohort study.
Patients of ≥18 years old receiving medical care at a large, academic, urban US medical centre between 2002-2016.
Inclusion criteria were a serum thyroid stimulating hormone (TSH) concentration of <0·3 mIU/l or ICD-9 code for thyrotoxicosis, with thyrotoxicosis confirmed by either a concurrent elevated serum triiodothyronine (T3) or thyroxine (T4) concentration ([total or free] within 3 months), and an available liver biochemical test(s) within 6 months of thyrotoxicosis. The biochemical liver tests assessed were serum aspartate transaminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (AP), gamma-glutamyltransferase (GGT), total bilirubin, and conjugated bilirubin concentrations.
In this cohort of 1514 subjects, the overall incidence of any biochemical liver test abnormality within 6 months of thyrotoxicosis was 39%. An initial serum TSH concentration <0·02 mIU/l, male gender, and African-American race were significant predictors of an abnormal serum liver biochemical test within 6 months of the diagnosis of new-onset untreated thyrotoxicosis.
This study identifies risk factors for patients who develop an abnormal serum liver biochemical test result within 6 months of a diagnosis of untreated thyrotoxicosis.
在未经治疗的甲状腺毒症患者中,血清肝功能检查异常很常见,甚至在开始使用可能会加重血清肝脏生化指标异常严重程度的抗甲状腺药物之前就已出现。已发表文献中这些异常的发生率差异很大。本研究的目的是评估新诊断的甲状腺毒症患者发生肝脏生化检查异常的危险因素及甲状腺毒症严重程度阈值。
单机构回顾性队列研究。
2002年至2016年期间在美国一家大型学术性城市医疗中心接受治疗的18岁及以上患者。
纳入标准为血清促甲状腺激素(TSH)浓度<0.3 mIU/l或甲状腺毒症的ICD-9编码,且通过同时升高的血清三碘甲状腺原氨酸(T3)或甲状腺素(T4)浓度([总或游离]在3个月内)确诊甲状腺毒症,以及在甲状腺毒症发生后6个月内可获得肝脏生化检查结果。评估的肝脏生化检查包括血清天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、碱性磷酸酶(AP)、γ-谷氨酰转移酶(GGT)、总胆红素和结合胆红素浓度。
在这1514名受试者的队列中,甲状腺毒症发生后6个月内任何肝脏生化检查异常的总体发生率为39%。初始血清TSH浓度<0.02 mIU/l、男性性别和非裔美国人种族是新诊断的未经治疗的甲状腺毒症患者在诊断后6个月内血清肝脏生化检查异常的显著预测因素。
本研究确定了未经治疗的甲状腺毒症患者在诊断后6个月内出现血清肝脏生化检查异常结果的危险因素。