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多发性硬化症中的乳糜泻患病率。

Prevalence of celiac disease in multiple sclerosis.

机构信息

Hospital Universitario Central de Asturias, 33006 Oviedo, Spain.

出版信息

BMC Neurol. 2011 Mar 7;11:31. doi: 10.1186/1471-2377-11-31.

DOI:10.1186/1471-2377-11-31
PMID:21385364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065402/
Abstract

BACKGROUND

Celiac disease (CD) is a common systemic disease related to a permanent intolerance to gluten and is often associated with different autoimmune and neurological diseases. Its mean prevalence in the general population is 1-2% worldwide. Our aim was to study the prevalence of celiac disease in a prospective series of Multiple Sclerosis (MS) patients and their first-degree relatives.

METHODS

We analyzed the prevalence of serological, histological and genetic CD markers in a series of 72 MS patients and in their 126 first-degree relatives, compared to 123 healthy controls.

RESULTS

Tissue IgA-anti-transglutaminase-2 antibodies were positive in 7 MS patients (10%), compared to 3 healthy controls (2.4%) (p < 0.05). OR: 5.33 (CI-95%: 1.074-26.425). No differences were found in HLA-DQ2 markers between MS patients (29%) and controls (26%) (NS).We detected mild or moderate villous atrophy (Marsh III type) in duodenal biopsies, in 8 MS patients (11.1%). We also found a high proportion of CD among first-degree relatives: 23/126 (32%). Several associated diseases were detected, mainly dermatitis 41 (57%) and iron deficiency anemia in 28 (39%) MS patients. We also found in them, an increased frequency of circulating auto-antibodies such as anti-TPO in 19 (26%), ANA in 11 (15%) and AMA in 2 (3%).

CONCLUSIONS

We have found an increased prevalence of CD in 8 of the 72 MS patients (11.1%) and also in their first-degree relatives (23/126 [32%]). Therefore, increased efforts aimed at the early detection and dietary treatment of CD, among antibody-positive MS patients, are advisable.

摘要

背景

乳糜泻(CD)是一种与麸质永久不耐受有关的常见全身性疾病,常与不同的自身免疫性和神经退行性疾病相关。其在全球普通人群中的平均患病率为 1-2%。我们的目的是研究乳糜泻在一系列多发性硬化症(MS)患者及其一级亲属中的患病率。

方法

我们分析了 72 例 MS 患者及其 126 名一级亲属的血清学、组织学和遗传学 CD 标志物的患病率,并与 123 名健康对照者进行比较。

结果

7 例 MS 患者(10%)的组织 IgA-抗转谷氨酰胺酶-2 抗体阳性,而 3 例健康对照者(2.4%)阳性(p<0.05)。OR:5.33(95%CI:1.074-26.425)。MS 患者(29%)与对照组(26%)之间的 HLA-DQ2 标志物无差异(NS)。我们在 8 例 MS 患者(11.1%)的十二指肠活检中发现了轻度或中度绒毛萎缩(Marsh III 型)。我们还发现一级亲属中 CD 的比例较高:126 例中有 23 例(32%)。在 MS 患者中发现了多种相关疾病,主要是皮炎 41 例(57%)和铁缺乏性贫血 28 例(39%)。我们还发现他们的循环自身抗体如抗 TPO 19 例(26%)、ANA 11 例(15%)和 AMA 2 例(3%)的频率增加。

结论

我们发现 72 例 MS 患者中有 8 例(11.1%)和他们的一级亲属(23/126 [32%])的 CD 患病率增加。因此,建议对抗体阳性的 MS 患者进行更多的努力,以早期发现和饮食治疗 CD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b62/3065402/07a3dca5e955/1471-2377-11-31-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b62/3065402/de3df1936959/1471-2377-11-31-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b62/3065402/07a3dca5e955/1471-2377-11-31-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b62/3065402/de3df1936959/1471-2377-11-31-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b62/3065402/07a3dca5e955/1471-2377-11-31-2.jpg

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