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系统性硬化症患者队列的营养状况和骨微观结构。

Nutritional Status and Bone Microarchitecture in a Cohort of Systemic Sclerosis Patients.

机构信息

Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine DiMI, University of Genoa, IRCCS San Martino Polyclinic, 16126 Genoa, Italy.

Clinical Nutrition Unit, IRCCS San Martino Polyclinic, 16132 Genoa, Italy.

出版信息

Nutrients. 2020 Jun 1;12(6):1632. doi: 10.3390/nu12061632.

Abstract

Systemic sclerosis (SSc) is a connective tissue disease characterized by initial microvascular damage, immune system activation and progressive fibrosis with insufficiency of internal organs. Gastrointestinal (GI) involvement is characterized by atrophy of the smooth muscle and small bowel hypomotility, mainly resulting from an autonomic nerve dysfunction. These modifications significantly affect gut transit and nutrient absorption, thus leading to malnutrition deficit induced by malabsorption. Nutritional deficit induced by malabsorption might also lead to bone alterations. This study aims to evaluate the relationship between malnutrition and bone status. Thirty-six postmenopausal female patients fulfilling the ACR 2013 criteria for SSc underwent dual-energy X-ray absorptiometry scan (DXA) to detect quantitative lumbar spine bone mineral density (BMD) and trabecular bone score (TBS) analysis to detect bone quality. Data from DXA also allow to assess body composition and provide several quantitative parameters, including free fat mass index (FFMI) that identifies the patient with malnutrition (values <15 kg/m in women and 17 kg/m in men), according to the ESPEN criteria. Body mass index (BMI) was calculated for all SSc patients and every patient completed a diary reporting GI symptoms. Two groups of SSc patients with or without diagnosed malnutrition according to FFMI parameter were identified. Malnourished SSc patients showed significantly lower weight ( = 0.01) and BMI ( = 0.001), as well as lower serum levels of hemoglobin ( = 0.009), albumin ( = 0.002), PTH ( = 0.02) and 25OH-vitamin D ( = 0.008). DXA analysis showed significantly lower lumbar L1-L4 T-score ( = 0.009) and BMD values ( = 0.029) in malnourished SSc patients. Consistently, TBS values were significantly lower in malnourished patients ( = 0.008) and correlated with BMD (at any site) and serum albumin levels ( = 0.02). In addition, FFMI positively correlated with bone parameters as well as with symptoms of intestinal impairment in malnourished SSc patients. Finally, GI symptoms significantly correlated with BMD but not with TBS. This pilot study shows that in malnourished SSc patients (2015 ESPEN criteria: FFMI<15 kg/m), an altered bone status significantly correlates with GI involvement, in terms of symptoms being mainly due to intestinal involvement together with the presence of selected serum biomarkers of malnutrition.

摘要

系统性硬化症(SSc)是一种结缔组织疾病,其特征为最初的微血管损伤、免疫系统激活和进行性纤维化,导致内脏器官功能不全。胃肠道(GI)受累表现为平滑肌萎缩和小肠蠕动不足,主要由自主神经功能障碍引起。这些改变显著影响肠道转运和营养吸收,从而导致由吸收不良引起的营养不良。由吸收不良引起的营养不良也可能导致骨骼改变。本研究旨在评估营养不良和骨骼状态之间的关系。36 名符合 ACR 2013 年 SSc 标准的绝经后女性患者接受了双能 X 线吸收法(DXA)扫描,以检测腰椎骨矿物质密度(BMD)定量和小梁骨评分(TBS)分析,以检测骨质量。DXA 数据还可以评估身体成分并提供多个定量参数,包括游离脂肪质量指数(FFMI),根据 ESPEN 标准,该指数可识别营养不良的患者(女性<15kg/m,男性<17kg/m)。为所有 SSc 患者计算了体重指数(BMI),每位患者都填写了一份报告胃肠道症状的日记。根据 FFMI 参数确定了有无营养不良的两组 SSc 患者。营养不良的 SSc 患者体重明显较低( = 0.01)和 BMI 较低( = 0.001),血红蛋白( = 0.009)、白蛋白( = 0.002)、甲状旁腺激素( = 0.02)和 25-羟维生素 D( = 0.008)的血清水平也较低。DXA 分析显示,营养不良的 SSc 患者腰椎 L1-L4 T 评分( = 0.009)和 BMD 值( = 0.029)明显较低。同样,营养不良患者的 TBS 值明显较低( = 0.008),并与 BMD(任何部位)和血清白蛋白水平相关( = 0.02)。此外,FFMI 与骨参数以及营养不良 SSc 患者的肠道损伤症状呈正相关。最后,GI 症状与 BMD 显著相关,但与 TBS 无关。这项初步研究表明,在营养不良的 SSc 患者(2015 年 ESPEN 标准:FFMI<15kg/m)中,骨状态的改变与胃肠道受累显著相关,其症状主要由肠道受累以及一些营养不良的血清生物标志物引起。

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