Bril Fernando, Portillo Sanchez Paola, Lomonaco Romina, Orsak Beverly, Hecht Joan, Tio Fermin, Cusi Kenneth
Division of Endocrinology, Diabetes and Metabolism, University of Florida, Gainesville, Florida 32610.
Malcom Randall Veterans Affairs Medical Center, Gainesville, Florida 32608.
J Clin Endocrinol Metab. 2017 Aug 1;102(8):2950-2961. doi: 10.1210/jc.2017-00867.
Patients with nonalcoholic fatty liver disease have a high cardiovascular risk, but statins are rarely prescribed because of fear of hepatotoxicity.
To prospectively assess the long-term safety of statins in patients with prediabetes/type 2 diabetes mellitus (T2DM) and nonalcoholic steatohepatitis (NASH).
Post hoc analysis of statin use during a randomized, controlled trial assessing pioglitazone vs placebo for NASH.
A total of 101 patients (86 receiving statins) with biopsy-proven NASH and prediabetes/T2DM were followed for up to 36 months.
Oral glucose tolerance test and percutaneous liver biopsy (baseline, month 18, and month 36); liver magnetic resonance spectroscopy and euglycemic insulin clamp (baseline and month 18).
Histologic and biochemical safety of statin use among patients with NASH.
Only 37% of patients were receiving statins at enrollment despite their high cardiovascular risk. Statin nonusers had higher plasma alanine aminotransferase levels but similar histologic severity of liver disease at baseline. In both statin users and nonusers, the same number of patients (n = 4) had a twofold or greater increase in plasma aminotransferases during follow-up. One statin nonuser was discontinued from the study because of this elevation. Values returned to normal without any active measure in all other cases. No changes on liver histology or hepatic insulin resistance were observed in patients with NASH newly started on a statin and receiving placebo during the main study.
Statin therapy is safe in patients with prediabetes/T2DM and NASH. Given their high cardiovascular risk, statin therapy should be encouraged in this population.
非酒精性脂肪性肝病患者心血管风险较高,但由于担心肝毒性,很少开具他汀类药物。
前瞻性评估他汀类药物在糖尿病前期/2型糖尿病(T2DM)和非酒精性脂肪性肝炎(NASH)患者中的长期安全性。
在一项评估吡格列酮与安慰剂治疗NASH的随机对照试验中,对他汀类药物的使用进行事后分析。
共有101例经活检证实为NASH且患有糖尿病前期/T2DM的患者(86例接受他汀类药物治疗),随访长达36个月。
口服葡萄糖耐量试验和经皮肝活检(基线、第18个月和第36个月);肝脏磁共振波谱和正常血糖胰岛素钳夹试验(基线和第18个月)。
NASH患者使用他汀类药物的组织学和生化安全性。
尽管心血管风险高,但仅37%的患者在入组时接受他汀类药物治疗。未使用他汀类药物的患者血浆丙氨酸转氨酶水平较高,但基线时肝病的组织学严重程度相似。在使用他汀类药物和未使用他汀类药物的患者中,随访期间血浆转氨酶升高两倍或更多的患者数量相同(n = 4)。一名未使用他汀类药物的患者因这种升高而退出研究。在所有其他病例中,无需采取任何积极措施,数值即可恢复正常。在主要研究期间新开始使用他汀类药物并接受安慰剂的NASH患者中,未观察到肝脏组织学或肝脏胰岛素抵抗的变化。
他汀类药物治疗在糖尿病前期/T2DM和NASH患者中是安全的。鉴于该人群心血管风险高,应鼓励在该人群中使用他汀类药物治疗。