HPB Surgery, Department of Surgery, Carolinas Medical Center, 1025 Morehead Medical Drive, Suite 600, Charlotte, NC, 28204, USA.
Obes Surg. 2014 Jan;24(1):15-21. doi: 10.1007/s11695-013-1044-6.
Nonalcoholic fatty liver disease (NAFLD) represents the most common cause of chronic liver disease in the USA. Biopsy has been the standard for determining fibrosis but is invasive, costly, and associated with risk. Previous studies report a calculated "NAFLD fibrosis scores" (cNFS) as a means to overcome the need for biopsy. We compared cNFS versus biopsy-pathological scoring for patients undergoing bariatric surgery.
We retrospectively reviewed patients with available preoperative labs and patient information undergoing Roux-en-Y gastric bypass (RYGBP) surgery at a single institution over a 5.5-year period. Biopsy samples were blind scored by a single hepatopathologist and compared with scores calculated using a previously reported cNFS.
Of the 225 patients that met the inclusion criteria, the mean body mass index was 44.6 ± 5.4 kg/m(2) and 85 % were female. Using the cNFS, 39.6 % of patients were categorized into low fibrosis, 52 % indeterminate, and 8.4 % high fibrosis groups. Analysis of fibrosis by pathology scoring demonstrated 2 of 89 (2.2 %) and 7 of 110 (3.4 %) had significant fibrosis in the low and intermediate groups, respectively. Conversely, in the high fibrosis group calculated by cNFS, only 6 of 19 (31.6 %) exhibited significant fibrosis by pathology scoring.
No definitive model for accurately predicting presence of NAFLD and fibrosis currently exits. Furthermore, under no circumstances should a clinical "NAFLD fibrosis score" replace liver biopsy at this time for RYGBP patients.
非酒精性脂肪性肝病(NAFLD)是美国最常见的慢性肝病病因。肝活检一直是确定纤维化的金标准,但具有侵袭性、昂贵且存在风险。既往研究报道了一种计算性“NAFLD 纤维化评分”(cNFS),以克服肝活检的需求。我们比较了 cNFS 与接受减重手术患者的肝活检病理评分。
我们回顾性分析了在一家机构接受 Roux-en-Y 胃旁路手术(RYGBP)的患者,这些患者在 5.5 年内有术前实验室检查和患者信息。对肝活检标本由一位单独的肝脏病理学家进行盲法评分,并与先前报道的 cNFS 计算的评分进行比较。
符合纳入标准的 225 例患者中,平均 BMI 为 44.6±5.4kg/m²,85%为女性。根据 cNFS,39.6%的患者被分为低纤维化组,52%为不确定纤维化组,8.4%为高纤维化组。通过病理评分分析纤维化程度,低纤维化组有 2/89(2.2%),中纤维化组有 7/110(3.4%)患者存在显著纤维化。相反,在 cNFS 计算的高纤维化组中,只有 6/19(31.6%)患者的病理评分显示存在显著纤维化。
目前尚无准确预测 NAFLD 和纤维化存在的明确模型。此外,在任何情况下,此时都不应仅凭临床“NAFLD 纤维化评分”替代 RYGBP 患者的肝活检。