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以n-3多不饱和脂肪酸作为单一疗法对非酒精性脂肪性肝病儿童进行长期治疗

Long-Term Treatment with n-3 Polyunsaturated Fatty Acids as a Monotherapy in Children with Nonalcoholic Fatty Liver Disease.

作者信息

Boyraz Mehmet, Pirgon Özgür, Dündar Bumin, Çekmez Ferhat, Hatipoğlu Nihal

机构信息

Süleyman Demirel University Faculty of Medicine, Department of Pediatric Endocrinology and Diabetes, Isparta, Turkey Phone: +90 246 211 93 02 E-mail:

出版信息

J Clin Res Pediatr Endocrinol. 2015 Jun;7(2):121-7. doi: 10.4274/jcrpe.1749.

DOI:10.4274/jcrpe.1749
PMID:26316434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4563183/
Abstract

OBJECTIVE

To investigate the efficacy and safety of n-3 polyunsaturated fatty acids (PUFA) treatment in obese children with nonalcoholic fatty liver disease (NAFLD).

METHODS

One hundred and eight obese (body mass index (BMI) >95th percentile for age and sex) adolescents with NAFLD were included in the study. Mean age of the subjects was 13.8 ± 3.9 years (9-17 yrs). The diagnosis of NAFLD was based on the presence of liver steatosis with high transaminases. The subjects were randomly divided into two groups. Group 1 (PUFA group, n=52) received a 1000 mg dose of PUFA once daily for 12 months and lifestyle intervention. Group 2 (placebo group, n=56) received a recommended diet plus placebo and lifestyle intervention for 12 months. Insulin resistance was evaluated by homeostasis model assessment of insulin resistance (HOMA-IR) from fasting samples.

RESULTS

BMI, fasting insulin levels and HOMA-IR values in both groups decreased significantly at the end of the study. In group 1, 67.8% of the patients had a decrease from baseline in the prevalence of steatosis (p<0.001). Frequency of elevated alanine aminotransferase (ALT) levels (39.2% to 14.2%; p<0.01) and elevated aspartate aminotransferase (AST) levels (25% to 17.8%; p=0.01) decreased significantly in the PUFA group. Following a 12-month diet plus placebo and lifestyle intervention treatment, 40.3% (21) of the patients in the placebo group also showed a decrease in frequency of steatosis (p=0.04) and slight decreases in frequency of elevated ALT levels (38.4% to 28.8%; p=0.01) and AST levels (30.7% to 28.8%; p>0.05).

CONCLUSION

Our results indicated that n-3 PUFA treatment is safe and efficacious in obese children with NAFLD and can improve ultrasonographic findings and the elevated transaminase levels.

摘要

目的

探讨n-3多不饱和脂肪酸(PUFA)治疗肥胖儿童非酒精性脂肪性肝病(NAFLD)的疗效及安全性。

方法

108例肥胖(体重指数(BMI)高于年龄和性别的第95百分位数)且患有NAFLD的青少年纳入本研究。受试者的平均年龄为13.8±3.9岁(9 - 17岁)。NAFLD的诊断基于存在肝脂肪变性且转氨酶升高。受试者被随机分为两组。第1组(PUFA组,n = 52)每天服用1000 mg剂量的PUFA,共12个月,并进行生活方式干预。第2组(安慰剂组,n = 56)接受推荐饮食加安慰剂及生活方式干预,为期12个月。通过空腹样本的胰岛素抵抗稳态模型评估(HOMA-IR)来评估胰岛素抵抗。

结果

研究结束时,两组的BMI、空腹胰岛素水平和HOMA-IR值均显著下降。在第1组中,67.8%的患者脂肪变性患病率较基线有所下降(p<0.001)。PUFA组中丙氨酸转氨酶(ALT)水平升高的频率(从39.2%降至14.2%;p<0.01)和天冬氨酸转氨酶(AST)水平升高的频率(从25%降至17.8%;p = 0.01)显著降低。经过12个月的饮食加安慰剂及生活方式干预治疗后,安慰剂组中40.3%(21例)的患者脂肪变性频率也有所下降(p = 0.04),ALT水平升高的频率略有下降(从38.4%降至28.8%;p = 0.01),AST水平升高的频率略有下降(从30.7%降至28.8%;p>0.05)。

结论

我们的结果表明,n-3 PUFA治疗对患有NAFLD的肥胖儿童是安全有效的,并且可以改善超声检查结果及转氨酶升高的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/6c1b8a5a9357/JCRPE-7-121-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/f80b811f86d4/JCRPE-7-121-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/5f4f0fda1b4c/JCRPE-7-121-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/0bd3e79e491d/JCRPE-7-121-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/6c1b8a5a9357/JCRPE-7-121-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/f80b811f86d4/JCRPE-7-121-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/5f4f0fda1b4c/JCRPE-7-121-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/0bd3e79e491d/JCRPE-7-121-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d658/4563183/6c1b8a5a9357/JCRPE-7-121-g6.jpg

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