Protective effects of 1-α-hydroxyvitamin D3 on residual β-cell function in patients with adult-onset latent autoimmune diabetes (LADA)

Protective effects of 1-α-hydroxyvitamin D3 on residual β-cell function in patients with adult-onset latent autoimmune diabetes (LADA)
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DOI:
10.1002/dmrr.977
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发表时间:
2009-07-01
影响因子:
8
通讯作者:
Zhou, Zhiguang
Zhou, Zhiguang
中科院分区:
医学2区
文献类型:
--
作者:
Li, Xia;Liao, Lan;Zhou, Zhiguang

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背景以往的体外和体内研究表明,维生素D可以防止胰腺β细胞的破坏,降低自身免疫性糖尿病的发病率。在患有1型糖尿病的儿童中,维生素D治疗对残余β细胞功能产生中度保护作用,并且已被证明是安全的。因此,我们假设维生素D可能对成人隐匿性自身免疫性糖尿病(LADA)患者的β细胞功能具有保护作用,LADA是一种缓慢进展的自身免疫性1型糖尿病。方法35例LADA患者随机分为单独皮下胰岛素组(n = 18)和胰岛素加1-α-羟基维生素D3组(n = 18)(1-α(OH)D3; 0.5 μ g/天)(n = 17)1年。结果在12个月的干预过程中,胰岛素+1-α(OH)D3组空腹和75 g葡萄糖负荷后2 h血浆G肽水平保持稳定,而单纯胰岛素组空腹和75 g葡萄糖负荷后2 h血浆G肽水平下降(P = 0.006)。70%的1-α(OH)D3治疗患者在治疗1年后维持或增加了FCP浓度,而仅用胰岛素治疗的患者仅22%维持稳定的FCP水平(P < 0.01)。对糖尿病病程不同的LADA亚组的进一步分析表明,仅在糖尿病病程不超过1年的患者中,1-α(OH)D3加胰岛素组的胰岛β细胞功能得到了更好的保护(如FCP和PCP水平显著较高所反映的)。结论1-α(OH)D3联合胰岛素治疗LADA患者可保护胰岛β细胞功能。版权所有(c)2009约翰威利父子有限公司。
Background Previous in vitro and in vivo studies have demonstrated that vitamin D could prevent pancreatic beta-cell destruction and reduce the incidence of autoimmune diabetes. In children with type 1 diabetes, vitamin D treatment produces moderate protective effects on residual beta-cell function and has proven to be safe. Therefore, we hypothesized that vitamin D might have protective effects on beta-cell function in patients with latent autoimmune diabetes in adults (LADA), a form of slowly progressive autoimmune type 1 diabetes.Methods Thirty-five patients with LADA were randomly assigned to receive subcutaneous insulin alone (n = 18) or insulin plus 1-alpha-hydroxyvitamin D3 (1-alpha(OH)D3; 0.5 mu g per day) (n = 17) for 1 year. Plasma G-peptide levels in fasting state (FCP) and 2 h after 75-g glucose load (PCP) were measured every 6 months with radioimmunoassay.Results Both FCP and PCP levels stayed steady in the insulin plus 1-alpha(OH)D3 group, while FCP decreased in insulin-alone group (P = 0.006) during the 12-month intervention. Seventy percent of patients treated with 1-alpha(OH)D3 maintained or increased their FCP concentrations after 1 year of treatment, while only 22% of patients treated with insulin alone maintained stable FCP levels (P < 0.01). Further analysis on LADA subgroups with different durations of diabetes demonstrated that islet beta-cell function was better preserved (as reflected by significantly higher FCP and PCP levels) in the 1-alpha(OH)D3 plus insulin group only in patients with diabetes duration no longer than 1 year. No severe side effects were observed in any group.Conclusion Our data suggest that 1-alpha(OH)D3 plus insulin therapy can preserve pancreatic beta-cell function in patients with LADA. Copyright (c) 2009 John Wiley & Sons, Ltd.