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儿童期起病的垂体功能减退症患者骨矿物质密度分布及骨闪烁显像异常。

Abnormalities in bone mineral density distribution and bone scintigraphy in patients with childhood onset hypopituitarism.

作者信息

Kosowicz Jerzy, El Ali Ziad, Ziemnicka Katarzyna, Sowinski Jerzy

机构信息

Department of Endocrinology and Metabolism, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

J Clin Densitom. 2007 Jul-Sep;10(3):332-9. doi: 10.1016/j.jocd.2007.03.098. Epub 2007 Apr 30.

Abstract

The aim of our study was to evaluate the effects of long-life severe growth hormone deficiency on bone mineral density (BMD) and bone scintigraphy in adult patients with childhood onset (CO) hypopituitarism never treated with growth hormone. Our studies included 22 adult patients with CO hypopituitarism never treated with growth hormone (13 males and 9 females, aged 25-66 yr). The patients received replacement therapy with thyroxine, sex steroid hormones, and patients with secondary adrenocortical deficiency, hydrocortisone, but none of the patients had ever received GH treatment. In 22 patients, the total body with regional distribution of BMD, the lumbar spine L2-L4, and radial (33% site) BMD were determined by dual energy X-ray absorptiometry (DXA). In addition, 12 patients had the femoral neck BMD examined. In 10 cases, bone scintigraphy using 99-technetium labeled methylene diphosphonate was performed. Our studies revealed abnormalities, not yet described, in the regional distribution of BMD and bone scintigraphy in adults with CO hypopituitarism never treated with GH. In all patients, the results obtained from the total body showed definite disproportion in the regional distribution of BMD with a significantly advanced bone mineral deficit in the legs and a moderate deficit in the arms and total body. Local BMD measured at the radial (33% site) and lumbar spine L2-L4 revealed also a more pronounced bone mineral deficit in the cortical bone (33% distal radius) than in the trabecular bone (spine L2-L4). Bone scintigraphy showed a decrease in tracer accumulation in the shafts of the long bones but normal uptake in the spine, ribs, sternum, skull, and periarticular areas, indicating suppressed skeletal metabolism of cortical bone. Our studies indicate that long-life growth hormone deficiency leads to deficient and abnormal distribution of bone mineralization, a more pronounced deficit of BMD at the cortical bone, mainly expressed in the shafts of the long bones of the legs and arms, and moderately reduced BMD at the trabecular bone. Bone scans displaying low diphosphonates uptake in the shafts of the long bones point to greatly suppressed skeletal metabolism of the cortical bone in the patients with CO hypopituitarism never treated with GH.

摘要

我们研究的目的是评估长期严重生长激素缺乏对成年期起病(CO)的垂体功能减退症且从未接受过生长激素治疗的患者骨密度(BMD)和骨闪烁显像的影响。我们的研究纳入了22例成年期起病的垂体功能减退症且从未接受过生长激素治疗的患者(13例男性和9例女性,年龄25 - 66岁)。患者接受甲状腺素、性激素替代治疗,继发性肾上腺皮质功能减退的患者接受氢化可的松治疗,但所有患者均从未接受过生长激素治疗。对22例患者采用双能X线吸收法(DXA)测定全身及各区域的骨密度,包括腰椎L2 - L4和桡骨(33%部位)骨密度。此外,对12例患者检测了股骨颈骨密度。对10例患者进行了使用99锝标记亚甲基二膦酸盐的骨闪烁显像。我们的研究揭示了成年期起病的垂体功能减退症且从未接受过生长激素治疗的患者在骨密度区域分布和骨闪烁显像方面存在尚未见报道的异常。在所有患者中,全身检测结果显示骨密度区域分布明显不均衡,腿部骨矿物质缺乏显著进展,手臂和全身存在中度缺乏。在桡骨(33%部位)和腰椎L2 - L4测量的局部骨密度显示,皮质骨(桡骨远端33%)的骨矿物质缺乏比小梁骨(脊柱L2 - L4)更明显。骨闪烁显像显示长骨干中示踪剂积聚减少,但脊柱、肋骨、胸骨、颅骨和关节周围区域摄取正常,表明皮质骨的骨骼代谢受到抑制。我们的研究表明,长期生长激素缺乏导致骨矿化分布不足和异常,皮质骨骨密度缺乏更明显,主要表现在腿部和手臂长骨干中,小梁骨骨密度中度降低。骨扫描显示长骨干中二膦酸盐摄取低,表明从未接受过生长激素治疗的成年期起病的垂体功能减退症患者皮质骨的骨骼代谢受到极大抑制。

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