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复发性阿弗他口炎患者血清胰岛素样生长因子1升高。

Elevated serum insulin-like growth factor 1 in recurrent aphthous stomatitis.

作者信息

Baccaglini Lorena, Shuster Jonathan J, Theriaque Douglas W, Naveed Zaeema

机构信息

Department of Epidemiology, College of Public Health University of Nebraska Medical Center Omaha Nebraska.

Health Outcomes and Policy, College of Medicine University of Florida Gainesville Florida.

出版信息

Clin Exp Dent Res. 2019 Mar 27;5(3):269-275. doi: 10.1002/cre2.181. eCollection 2019 Jun.

Abstract

Over 100 million Americans experience recurrent aphthous stomatitis (RAS) at some point in life. To develop targeted drugs for RAS treatment, it is critical to identify its etiology. We determined if serum insulin-like growth factor 1 (IGF-1) and related factors are associated with RAS, because both RAS prevalence and IGF-1 are highest during puberty. We analyzed data from 1,480 Third National Health and Nutrition Examination Survey participants aged 20-40 years. Participants with a history of diabetes or lupus, cotinine levels 6 ng/ml or higher or glycemia 110 mg/dl or higher were excluded. We compared levels of IGF-1, IGFBP-3, leptin, and insulin in participants with a positive vs. negative RAS history in the prior 12 months. We used logistic regression in SAS/SUDAAN to account for the complex sampling design. The odds of a positive RAS history were 1.31 times higher for every 100 ng/ml increase in serum IGF-1. This association persisted after adjustment for age, race/ethnicity, medication intake, body mass index, insulin, leptin, glycemia, and income (adjusted OR = 1.30, 95% CI [1.06, 1.60];  = 0.013). The odds of a positive RAS history were also higher among non-Hispanic white compared with non-Hispanic black participants (adjusted OR = 4.37, 95% CI [3.00, 6.38]). Leptin, IGFBP-3, and insulin levels did not differ by RAS status. The significantly higher IGF-1 levels in participants with a positive RAS history compared with controls suggest a possible role of the IGF-1 pathway in RAS etiology.

摘要

超过1亿美国人在人生的某个阶段经历过复发性阿弗他口炎(RAS)。为了开发用于治疗RAS的靶向药物,确定其病因至关重要。我们研究血清胰岛素样生长因子1(IGF-1)及相关因子是否与RAS有关,因为RAS患病率和IGF-1在青春期均处于最高水平。我们分析了来自1480名年龄在20至40岁的第三次全国健康与营养检查调查参与者的数据。排除有糖尿病或狼疮病史、可替宁水平6 ng/ml或更高或血糖110 mg/dl或更高的参与者。我们比较了在过去12个月中有RAS病史阳性与阴性的参与者的IGF-1、IGFBP-3、瘦素和胰岛素水平。我们在SAS/SUDAAN中使用逻辑回归来考虑复杂的抽样设计。血清IGF-1每增加100 ng/ml,RAS病史阳性的几率就高1.31倍。在调整年龄、种族/民族、药物摄入、体重指数、胰岛素、瘦素、血糖和收入后,这种关联仍然存在(调整后的OR = 1.30,95% CI [1.06, 1.60];P = 0.013)。与非西班牙裔黑人参与者相比(调整后的OR = 4.37,95% CI [;3.00, 6.38]),非西班牙裔白人中RAS病史阳性的几率也更高。瘦素、IGFBP-3和胰岛素水平在RAS状态方面没有差异。与对照组相比,有RAS病史阳性的参与者中IGF-1水平显著更高,这表明IGF-1通路在RAS病因中可能发挥作用。

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