Siegel Joanna L, Jorgensen Roberta, Angulo Paul, Lindor Keith D
Division of Gastroenterology and Hepatology, Mayo Clinic and Foundation Rochester, Minnesota 55905, USA.
J Clin Gastroenterol. 2003 Aug;37(2):183-5. doi: 10.1097/00004836-200308000-00018.
Ursodeoxycholic acid (UDCA) is the established treatment of primary biliary cirrhosis (PBC) and is a safe and well-tolerated medication. Nevertheless, patients often anecdotally complain of weight gain while on this drug.
We compared weight changes in patients treated with UDCA and those on placebo to characterize this potential side effect.
One-hundred eighty patients with PBC who were enrolled into a randomized, controlled trial received either UDCA (13-15 mg/kg/d) or an identical placebo. Changes from baseline weight were calculated at 12, 24, 36, and 48 months. Other markers of disease activity, including liver biochemistries, serum lipids, histologic stage, and Mayo Risk Score were evaluated in both groups.
The proportion of patients who gained weight during the first 12 months of therapy was significantly greater in the UDCA than placebo group (67/86 [78%] versus 43/73 [57%] respectively, P = 0.005). Patients in the UDCA group gained an average of 3.6 +/- 6.5% kg (2.2 +/- 5.1 kg) which was significantly greater than the average of 0.6 +/- 6.9% kg (0.6 +/- 4.9 kg) gained in the placebo group (P = 0.04). The biggest change in weight occurred in the first 12 months of treatment (P < 0.001); after this, weight was maintained for the 4-year duration of treatment. There was no significant correlation between initial body mass index (BMI) and weight change or changes in disease activity and weight.
UDCA treatment in patients with PBC is associated with a significant weight gain that occurs in the first 12 months of treatment, persists for the duration of treatment, and occurs independent of baseline BMI. Discussions with PBC patients beginning UDCA treatment should include the beneficial effects this medication has on disease outcome, but should also mention weight gain as a possible side effect.
熊去氧胆酸(UDCA)是原发性胆汁性肝硬化(PBC)的既定治疗药物,是一种安全且耐受性良好的药物。然而,患者常称服用此药后体重增加。
我们比较了接受UDCA治疗的患者与接受安慰剂治疗的患者的体重变化,以明确这种潜在的副作用。
180例纳入随机对照试验的PBC患者接受了UDCA(13 - 15毫克/千克/天)或相同的安慰剂治疗。在第12、24、36和48个月计算相对于基线体重的变化。对两组患者的其他疾病活动指标进行了评估,包括肝脏生化指标、血脂、组织学分期和梅奥风险评分。
在治疗的前12个月体重增加的患者比例,UDCA组显著高于安慰剂组(分别为67/86 [78%] 对43/73 [57%],P = 0.005)。UDCA组患者平均体重增加3.6 +/- 6.5%千克(2.2 +/- 5.1千克),显著高于安慰剂组平均增加的0.6 +/- 6.9%千克(0.6 +/- 4.9千克)(P = 0.04)。体重的最大变化发生在治疗的前12个月(P < 0.001);此后,在4年的治疗期间体重保持稳定。初始体重指数(BMI)与体重变化或疾病活动变化与体重之间无显著相关性。
PBC患者接受UDCA治疗与治疗的前12个月出现显著体重增加有关,且在整个治疗期间持续存在,与基线BMI无关。在与开始接受UDCA治疗的PBC患者讨论时,应提及该药物对疾病转归的有益作用,但也应提及体重增加这一可能的副作用。