Brophy Sinead, Davies Helen, Mannan Sopna, Brunt Huw, Williams Rhys
College of Medicine, University of Wales, Swansea, Singleton Park, Swansea, Wales, UK, SA2 8PP.
Cochrane Database Syst Rev. 2011 Sep 7;2011(9):CD006165. doi: 10.1002/14651858.CD006165.pub3.
Latent autoimmune diabetes in adults (LADA) is a slowly developing type 1 diabetes.
To compare interventions used for LADA.
Studies were obtained from searches of electronic databases, supplemented by handsearches, conference proceedings and consultation with experts. Date of last search was December 2010.
Randomised controlled trials (RCT) and controlled clinical trials (CCT) evaluating interventions for LADA or type 2 diabetes with antibodies were included.
Two authors independently extracted data and assessed risk of bias. Studies were summarised using meta-analysis or descriptive methods.
Searches identified 13,306 citations. Fifteen publications (ten studies) were included, involving 1019 participants who were followed between three months to 10 years (1060 randomised). All studies had a high risk of bias. Sulphonylurea (SU) with insulin did not improve metabolic control significantly more than insulin alone at three months (one study, n = 15) and at 12 months (one study, n = 14) of treatment and follow-up. SU (with or without metformin) gave poorer metabolic control compared to insulin alone (mean difference in glycosylated haemoglobin A1c (HbA1c) from baseline to end of study, for insulin compared to oral therapy: -1.3% (95% confidence interval (CI) -2.4 to -0.1; P = 0.03, 160 participants, four studies, follow-up/duration of therapy: 12, 30, 36 and 60 months; however, heterogeneity was considerable). In addition, there was evidence that SU caused earlier insulin dependence (proportion requiring insulin at two years was 30% in the SU group compared to 5% in conventional care group (P < 0.001); patients classified as insulin dependent was 64% (SU group) and 12.5% (insulin group, P = 0.007). No intervention influenced fasting C-peptide, but insulin maintained stimulated C-peptide better than SU (one study, mean difference 7.7 ng/ml (95% CI 2.9 to 12.5)). In a five year follow-up of GAD65 (glutamic acid decarboxylase formulated with aluminium hydroxide), improvements in fasting and stimulated C-peptide levels (20 μg group) were maintained after five years. Short term (three months) follow-up in one study (n = 74) using Chinese remedies did not demonstrate a significant difference in improving fasting C-peptide levels compared to insulin alone (0.07 µg/L (95% CI -0.05 to 0.19). One study using vitamin D with insulin showed steady fasting C-peptide levels in the vitamin D group but declining fasting C-peptide levels (368 to 179 pmol/L, P = 0.006) in the insulin alone group at 12 months follow-up. Comparing studies was difficult as there was a great deal of heterogeneity in the studies and in their selection criteria. There was no information regarding health-related quality of life, complications of diabetes, cost or health service utilisation, mortality and limited evidence on adverse events (studies on oral agents or insulin reported no adverse events in terms of severe hypoglycaemic episodes).
AUTHORS' CONCLUSIONS: Two studies show SU leading to earlier insulin dependence and a meta-analysis of four studies with considerable heterogeneity showed poorer metabolic control if SU is prescribed for patients with LADA compared to insulin. One study showed that vitamin D with insulin may protect pancreatic beta cells in LADA. Novel treatments such as GAD65 in certain doses (20 μg) have been suggested to maintain fasting and stimulated C-peptide levels. However, there is no significant evidence for or against other lines of treatment of LADA.
成人隐匿性自身免疫性糖尿病(LADA)是一种缓慢进展的1型糖尿病。
比较用于LADA的干预措施。
通过电子数据库检索获取研究,并辅以手工检索、会议论文集和专家咨询。最后一次检索日期为2010年12月。
纳入评估LADA或伴有抗体的2型糖尿病干预措施的随机对照试验(RCT)和对照临床试验(CCT)。
两位作者独立提取数据并评估偏倚风险。采用荟萃分析或描述性方法对研究进行总结。
检索共识别出13306条引文。纳入15篇出版物(10项研究),涉及1019名参与者,随访时间为3个月至10年(1060名随机分组)。所有研究均存在较高的偏倚风险。在治疗和随访3个月(1项研究,n = 15)及12个月(1项研究,n = 14)时,磺脲类药物(SU)联合胰岛素在改善代谢控制方面并不比单纯胰岛素显著更优。与单纯胰岛素相比,SU(加或不加二甲双胍)的代谢控制更差(糖化血红蛋白A1c(HbA1c)从基线到研究结束的平均差值,胰岛素组与口服治疗组相比:-1.3%(95%置信区间(CI)-2.4至-0.1;P = 0.03,160名参与者,4项研究,随访/治疗持续时间:12、30、36和60个月;然而,异质性相当大)。此外,有证据表明SU导致更早出现胰岛素依赖(SU组两年时需要胰岛素的比例为30%,而传统治疗组为5%(P < 0.001);分类为胰岛素依赖的患者SU组为64%(SU组)和12.5%(胰岛素组,P = 0.007)。没有干预措施影响空腹C肽,但胰岛素在维持刺激后C肽方面优于SU(1项研究,平均差值7.7 ng/ml(95%CI 2.9至12.5))。在对用氢氧化铝配制谷氨酸脱羧酶(GAD65)进行的五年随访中,五年后空腹和刺激后C肽水平(20μg组)仍保持改善。一项使用中药的研究(n = 74)进行的短期(3个月)随访未显示与单纯胰岛素相比在改善空腹C肽水平方面有显著差异(0.07µg/L(95%CI -0.05至0.19))。一项使用维生素D联合胰岛素的研究显示,维生素D组空腹C肽水平稳定,而单纯胰岛素组在12个月随访时空腹C肽水平下降(从368至179 pmol/L,P = 0.006)。由于研究及其选择标准存在大量异质性,比较研究很困难。没有关于健康相关生活质量、糖尿病并发症、成本或卫生服务利用、死亡率的信息,且关于不良事件的证据有限(关于口服药物或胰岛素的研究未报告严重低血糖事件方面的不良事件)。
两项研究表明SU导致更早出现胰岛素依赖,对四项异质性相当大的研究进行的荟萃分析显示,与胰岛素相比,为LADA患者开具SU时代谢控制更差。一项研究表明,维生素D联合胰岛素可能保护LADA患者的胰腺β细胞。已建议某些剂量(20μg)的新型治疗方法如GAD65可维持空腹和刺激后C肽水平。然而,对于LADA的其他治疗方法,没有支持或反对的显著证据。