Peña Alexia S, Wiltshire Esko, Gent Roger, Piotto Lino, Hirte Craig, Couper Jennifer
Endocrinology and Diabetes Department, Women's and Children's Hospital, 72 King William Rd., North Adelaide, SA 5006, Australia.
Diabetes Care. 2007 Aug;30(8):2122-7. doi: 10.2337/dc06-2505. Epub 2007 May 22.
Obese children have severe endothelial dysfunction as measured by flow-mediated dilation (FMD). We have shown that folic acid normalizes endothelial function in children with type 1 diabetes who have a similar degree of endothelial dysfunction but lower total plasma homocyst(e)ine (tHcy) and higher folate status. Our aim was to evaluate, for the first time, the effect of folate supplementation on endothelial dysfunction in obese children.
A total of 53 obese subjects (26 male, mean +/- SD age 13.3 +/- 2.2 years, and BMI Z score 2.29 +/- 0.25) participated in a randomized, double-blind, placebo-controlled, parallel trial of oral folic acid (5 mg/day) or placebo for 8 weeks. Before and after the intervention, we assessed endothelial function (FMD), smooth muscle function (glyceryl trinitrate-induced dilatation [GTN]), high-sensitivity C-reactive protein (hsCRP), tHcy, serum folate, red cell folate (RCF), and lipids.
There were no group differences at baseline. FMD did not change with the intervention (folic acid group pre- and postintervention: 6.42 +/- 5.03 and 6.56 +/- 4.79%, respectively, vs. placebo group: 5.17 +/- 3.54 and 5.79 +/- 4.26%, respectively; P = 0.6). Folate supplementation increased serum folate and RCF by 18.4 nmol/l (P < 0.001) and 240.1 nmol/l (P < 0.001), respectively, and decreased tHcy by 0.95 microl (P = 0.008). The intervention did not change GTN, hsCRP, or lipids.
Folic acid supplementation does not improve endothelial function in obese children without diabetes despite increasing folate status and reducing tHcy. This is in contrast to the response to folate in children with type 1 diabetes.
通过血流介导的血管舒张(FMD)测量发现,肥胖儿童存在严重的内皮功能障碍。我们已经表明,叶酸可使1型糖尿病儿童的内皮功能恢复正常,这些儿童具有相似程度的内皮功能障碍,但血浆总同型半胱氨酸(tHcy)水平较低且叶酸状态较高。我们的目的是首次评估补充叶酸对肥胖儿童内皮功能障碍的影响。
共有53名肥胖受试者(26名男性,平均年龄±标准差为13.3±2.2岁,BMI Z评分为2.29±0.25)参与了一项随机、双盲、安慰剂对照、平行试验,口服叶酸(5毫克/天)或安慰剂,为期8周。在干预前后,我们评估了内皮功能(FMD)、平滑肌功能(硝酸甘油诱导的血管舒张[GTN])、高敏C反应蛋白(hsCRP)、tHcy、血清叶酸、红细胞叶酸(RCF)和血脂。
基线时两组无差异。干预后FMD未发生变化(叶酸组干预前后分别为6.42±5.03%和6.56±4.79%,安慰剂组分别为5.17±3.54%和5.79±4.26%;P = 0.6)。补充叶酸分别使血清叶酸和RCF增加了18.4纳摩尔/升(P < 0.001)和240.1纳摩尔/升(P < 0.001),并使tHcy降低了0.95微摩尔(P = 0.008)。干预未改变GTN、hsCRP或血脂。
尽管补充叶酸可提高叶酸状态并降低tHcy,但对无糖尿病的肥胖儿童,补充叶酸并不能改善其内皮功能。这与1型糖尿病儿童对叶酸的反应不同。