Pacifico Lucia, Di Martino Michele, Anania Caterina, Andreoli Gian Marco, Bezzi Mario, Catalano Carlo, Chiesa Claudio
Lucia Pacifico, Caterina Anania, Gian Marco Andreoli, Department of Pediatrics and Child Neuropsychiatry, Sapienza University of Rome, 00161 Rome, Italy.
World J Gastroenterol. 2015 Apr 21;21(15):4688-95. doi: 10.3748/wjg.v21.i15.4688.
To analyze the associations of pancreatic fat with other fat depots and β-cell function in pediatric nonalcoholic fatty liver disease (NAFLD).
We examined 158 overweight/obese children and adolescents, 80 with NAFLD [hepatic fat fraction (HFF) ≥ 5%] and 78 without fatty liver. Visceral adipose tissue (VAT), pancreatic fat fraction (PFF) and HFF were determined by magnetic resonance imaging. Estimates of insulin sensitivity were calculated using the homeostasis model assessment of insulin resistance (HOMA-IR), defined by fasting insulin and fasting glucose and whole-body insulin sensitivity index (WBISI), based on mean values of insulin and glucose obtained from oral glucose tolerance test and the corresponding fasting values. Patients were considered to have prediabetes if they had either: (1) impaired fasting glucose, defined as a fasting glucose level ≥ 100 mg/dL to < 126 mg/dL; (2) impaired glucose tolerance, defined as a 2 h glucose concentration between ≥ 140 mg/dL and < 200 mg/dL; or (3) hemoglobin A1c value of ≥ 5.7% to < 6.5%.
PFF was significantly higher in NAFLD patients compared with subjects without liver involvement. PFF was significantly associated with HFF and VAT, as well as fasting insulin, C peptide, HOMA-IR, and WBISI. The association between PFF and HFF was no longer significant after adjusting for age, gender, Tanner stage, body mass index (BMI)-SD score, and VAT. In multiple regression analysis with WBISI or HOMA-IR as the dependent variables, against the covariates age, gender, Tanner stage, BMI-SD score, VAT, PFF, and HFF, the only variable significantly associated with WBISI (standardized coefficient B, -0.398; P = 0.001) as well as HOMA-IR (0.353; P = 0.003) was HFF. Children with prediabetes had higher PFF and HFF than those without. PFF and HFF were significantly associated with prediabetes after adjustment for clinical variables. When all fat depots where included in the same model, only HFF remained significantly associated with prediabetes (OR = 3.38; 95%CI: 1.10-10.4; P = 0.034).
In overweight/obese children with NAFLD, pancreatic fat is increased compared with those without liver involvement. However, only liver fat is independently related to prediabetes.
分析儿童非酒精性脂肪性肝病(NAFLD)中胰腺脂肪与其他脂肪储存库及β细胞功能的关联。
我们检查了158名超重/肥胖儿童和青少年,其中80名患有NAFLD(肝脂肪分数(HFF)≥5%),78名无脂肪肝。通过磁共振成像测定内脏脂肪组织(VAT)、胰腺脂肪分数(PFF)和HFF。使用胰岛素抵抗稳态模型评估(HOMA-IR)计算胰岛素敏感性估计值,HOMA-IR由空腹胰岛素和空腹血糖定义,全身胰岛素敏感性指数(WBISI)基于口服葡萄糖耐量试验获得的胰岛素和葡萄糖平均值及相应空腹值计算。如果患者有以下情况之一,则被认为患有糖尿病前期:(1)空腹血糖受损,定义为空腹血糖水平≥100mg/dL至<126mg/dL;(2)葡萄糖耐量受损,定义为2小时血糖浓度≥140mg/dL至<200mg/dL;或(3)糖化血红蛋白A1c值≥5.7%至<6.5%。
与无肝脏受累的受试者相比,NAFLD患者的PFF显著更高。PFF与HFF、VAT以及空腹胰岛素、C肽、HOMA-IR和WBISI显著相关。在调整年龄、性别、坦纳分期、体重指数(BMI)-标准差评分和VAT后,PFF与HFF之间的关联不再显著。在以WBISI或HOMA-IR为因变量的多元回归分析中,针对协变量年龄、性别、坦纳分期、BMI-标准差评分、VAT、PFF和HFF,与WBISI(标准化系数B,-0.398;P = 0.001)以及HOMA-IR(0.353;P = 0.003)显著相关的唯一变量是HFF。患有糖尿病前期的儿童比未患糖尿病前期的儿童PFF和HFF更高。在调整临床变量后,PFF和HFF与糖尿病前期显著相关。当所有脂肪储存库纳入同一模型时,只有HFF与糖尿病前期仍显著相关(OR = 3.38;95%CI:1.10 - 10.4;P = 0.034)。
在患有NAFLD的超重/肥胖儿童中,与无肝脏受累的儿童相比,胰腺脂肪增加。然而,只有肝脏脂肪与糖尿病前期独立相关。