Kavuncu V, Dundar Umit, Ciftci I H, Evcik D, Yigit I
Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Afyon Kocatepe University, Mavi Hastane, 03200, Afyonkarahisar, Turkey.
Rheumatol Int. 2009 May;29(7):841-5. doi: 10.1007/s00296-008-0797-z. Epub 2008 Nov 29.
Screening studies indicate a prevalence of celiac disease (CD) of up to 1% in populations of European ancestry, yet the majority of cases remain undiagnosed. One of the common complication of CD is intestinal osteopathy or osteoporosis [bone mineral density (BMD) based diagnosis]. Available data regarding the prevalence of CD in the patients with osteoporosis are limited and controversial. The objective of this study was to perform serological testing to screen for CD among postmenopausal women with osteoporosis. We studied 192 postmenopausal women with low BMD with a mean age of 62.75 +/- 8.58 years. Among the patients, a total of 137 had osteoporosis and 55 had osteopenia. Venous blood samples were obtained for serological screening of CD and evaluation of bone metabolism. The serological screening protocol consisted of determining serum level of IgA antigliadin antibodies (AGA), IgG-AGA, IgA endomysial antibody (EMA), IgG-EMA. Subjects who were positive for both IgA-AGA and IgA-EMA were classified as having CD. Bone metabolism was evaluated by serum calcium, phosphorus, alkaline phosphatase, parathyroid hormone, 25 (OH) vitamin D, osteocalcin, serum C-telopeptide cross-linked collagen type I levels. Of the 192 patients evaluated, only one (0.5%) was found to have positive for both IgA-AGA and IgA EMA tests and accepted as having CD. Prevelance of CD in postmenopausal women with low BMD (0.5%) did not differ from prevelance of CD in normal healthy population (0.3-1%). BMD values at proximal femur level were significantly lower in IgA-AGA (+) patients when compared to IgA-AGA (-) patients. However, the mean levels of bone metabolism markers were found similiar in both IgA-AGA (+) and (-) patients. In conclusion, the results of our study suggest that there is no need for routine screening of CD in postmenopausal women with osteoporosis.
筛查研究表明,在欧洲血统人群中,乳糜泻(CD)的患病率高达1%,但大多数病例仍未得到诊断。CD的常见并发症之一是肠道骨病或骨质疏松症(基于骨矿物质密度(BMD)的诊断)。关于骨质疏松症患者中CD患病率的现有数据有限且存在争议。本研究的目的是进行血清学检测,以筛查绝经后骨质疏松症女性中的CD。我们研究了192名BMD较低的绝经后女性,平均年龄为62.75±8.58岁。在这些患者中,共有137人患有骨质疏松症,55人患有骨质减少症。采集静脉血样本进行CD的血清学筛查和骨代谢评估。血清学筛查方案包括测定血清中抗麦醇溶蛋白抗体(AGA)的IgA水平、IgG-AGA、IgA肌内膜抗体(EMA)、IgG-EMA。IgA-AGA和IgA-EMA均呈阳性的受试者被归类为患有CD。通过血清钙、磷、碱性磷酸酶、甲状旁腺激素、25(OH)维生素D、骨钙素、血清I型胶原C末端交联肽水平评估骨代谢。在评估的192名患者中,只有一名(0.5%)被发现IgA-AGA和IgA EMA检测均呈阳性,并被确认为患有CD。BMD较低的绝经后女性中CD的患病率(0.5%)与正常健康人群中CD的患病率(0.3 - 1%)没有差异。与IgA-AGA(-)患者相比,IgA-AGA(+)患者股骨近端水平的BMD值显著更低。然而,在IgA-AGA(+)和(-)患者中,骨代谢标志物的平均水平相似。总之,我们的研究结果表明,绝经后骨质疏松症女性无需常规筛查CD。