Significant bone microarchitecture impairment in premenopausal women with active celiac disease

被引:30
作者
Belen Zanchetta, Maria [1 ,3 ]
Costa, Florencia [2 ]
Longobardi, Vanesa [1 ]
Longarini, Gabriela [2 ]
Martin Mazure, Roberto [2 ]
Laura Moreno, Maria [2 ]
Vazquez, Horacio [2 ]
Silveira, Fernando [1 ]
Niveloni, Sonia [2 ]
Smecuol, Edgard [2 ]
de la Paz Temprano, Maria [2 ]
Jer Hwang, Hui [2 ]
Gonzalez, Andrea [2 ]
Cesar Maurino, Eduardo [2 ]
Bogado, Cesar [1 ,3 ]
Zanchetta, Jose R. [1 ,3 ]
Cesar Bai, Julio [2 ,4 ]
机构
[1] IDIM, Buenos Aires, DF, Argentina
[2] Hosp Gastroenterol Dr C Bonorino Udaondo, Dept Med, Secc Intestino Delgado, Buenos Aires, DF, Argentina
[3] Univ Salvador, Catedra Osteol & Metab Mineral, Buenos Aires, DF, Argentina
[4] Univ Salvador, Fac Med, Catedra Gastroenterol, Buenos Aires, DF, Argentina
关键词
Bone microarchitecture; Celiac disease; HRp-QCT; Osteoporosis; Fractures; MINERAL DENSITY; BODY-COMPOSITION; FRACTURE RISK; METABOLISM; METAANALYSIS;
D O I
10.1016/j.bone.2015.03.005
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Patients with active celiac disease (CD) are more likely to have osteoporosis and increased risk of fractures. High-resolution peripheral quantitative computed tomography (HR-pQCT) permits three-dimensional exploration of bone microarchitectural characteristics measuring separately cortical and trabecular compartments, and giving a more profound insight into bone disease pathophysiology and fracture. We aimed to determine the volumetric and microarchitectural characteristics of peripheral bones-distal radius and tibia-in an adult premenopausal cohort with active CD assessed at diagnosis. We prospectively enrolled 31 consecutive premenopausal women with newly diagnosed CD (median age 29 years, range: 18-49) and 22 healthy women of similar age (median age 30 years, range 21-41) and body mass index. Compared with controls, peripheral bones of CD patients were significantly lower in terms of total volumetric density mg/cm(3) (mean +/- SD: 274.7 +/- 51.7 vs. 324.7 +/- 45.8, p 0.0006 at the radius; 264.4 +/- 48.7 vs. 307 +/- 40.7, p 0.002 at the tibia), trabecular density mg/cm(3) (118.6 +/- 31.5 vs. 161.9 +/- 33.6, p < 0.0001 at the radius; 127.9 +/- 28.7 vs. 157.6 +/- 15.6, p < 0.0001 at the tibia); bone volume/trabecular volume ratio % (9.9 +/- 2.6 vs. 13.5 +/- 2.8, p < 0.0001 at the radius; 10.6 +/- 2.4 vs. 13.1 +/- 1.3, p < 0.0001 at the tibia); number of trabeculae 1/mm (1.69 +/- 0.27 vs. 1.89 +/- 0.26, p 0.009 at the radius; 1.53 +/- 032 vs. 1.80 +/- 0.26, p 0.002 at the tibia); and trabecular thickness mm (0.058 +/- 0.010 vs. 0.071 +/- 0.008, p < 0.0001 at the radius with no significant difference at the tibia). Cortical density was significantly lower in both regions (D comp mg/cm(3) 860 +/- 57.2 vs. 893.9 +/- 43, p 0.02; 902.7 +/- 48.7 vs. 932.6 +/- 32.6, p 0.01 in radius and tibia respectively). Although cortical thickness was lower in CD patients, it failed to show any significant inter-group difference (a-8% decay with p 0.11 in both bones). Patients with symptomatic CD (n = 22) had a greater bone microarchitectural deficit than those with subclinical CD. HR-pQCT was used to successfully identify significant deterioration in the microarchitecture of trabecular and cortical compartments of peripheral bones. Impairment was characterized by lower trabecular number and thickness-which increased trabecular network heterogeneity-and lower cortical density and thickness. In the prospective follow-up of this group of patients we expect to be able to assess whether bone microarchitecture recovers and to what extend after gluten-free diet. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:149 / 157
页数:9
相关论文
共 38 条
[1]
[Anonymous], 2000, NIH Consens Statement, V17, P1
[2]
World Gastroenterology Organisation Global Guidelines on Celiac Disease [J].
Bai, Julio C. ;
Fried, Michael ;
Corazza, Gino R. ;
Schuppan, Detlef ;
Farthing, Michael ;
Catassi, Carlo ;
Greco, Luigi ;
Cohen, Henry ;
Ciacci, Carolina ;
Eliakim, Rami ;
Fasano, Alessio ;
Gonzalez, Andrea ;
Krabshuis, Justus H. ;
LeMair, Anton .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2013, 47 (02) :121-126
[3]
BODY-COMPOSITION AND CALCIUM-METABOLISM IN ADULT TREATED CELIAC-DISEASE [J].
BODE, S ;
HASSAGER, C ;
GUDMANDHOYER, E ;
CHRISTIANSEN, C .
GUT, 1991, 32 (11) :1342-1345
[4]
In vivo assessment of trabecular bone microarchitecture by high-resolution peripheral quantitative computed tomography [J].
Boutroy, S ;
Bouxsein, ML ;
Munoz, F ;
Delmas, PD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (12) :6508-6515
[5]
CARACENI MP, 1988, AM J GASTROENTEROL, V83, P274
[6]
Bones in coeliac disease:: diagnosis and treatment [J].
Corazza, GR ;
Di Stefano, M ;
Mauriño, E ;
Bai, JC .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2005, 19 (03) :453-465
[7]
BONE MASS AND METABOLISM IN PATIENTS WITH CELIAC-DISEASE [J].
CORAZZA, GR ;
DISARIO, A ;
CECCHETTI, L ;
TAROZZI, C ;
CORRAO, G ;
BERNARDI, M ;
GASBARRINI, G .
GASTROENTEROLOGY, 1995, 109 (01) :122-128
[8]
QCT-based finite element models predict human vertebral strength in vitro significantly better than simulated DEXA [J].
Dall'Ara, E. ;
Pahr, D. ;
Varga, P. ;
Kainberger, F. ;
Zysset, P. .
OSTEOPOROSIS INTERNATIONAL, 2012, 23 (02) :563-572
[9]
Positive celiac disease serology and reduced bone mineral density in adult women [J].
Duerksen, Donald R. ;
Leslie, William D. .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2010, 24 (02) :103-107
[10]
Analysis of the structure and strength of bones in celiac disease patients [J].
Ferretti, J ;
Mazure, R ;
Tanoue, P ;
Marino, A ;
Cointry, G ;
Vazquez, H ;
Niveloni, S ;
Pedreira, S ;
Mauriño, E ;
Zanchetta, J ;
Bai, JC .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (02) :382-390