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作 者:罗南萍[1] 刘恒国[1] 李金花[1] 胡成进[1]
机构地区:[1]解放军济南军区总医院实验诊断科,山东省济南市250031
出 处:《中国组织工程研究与临床康复》2008年第7期1247-1250,共4页Journal of Clinical Rehabilitative Tissue Engineering Research
摘 要:目的:观察老年男性代谢综合征患者骨密度与骨代谢指标含量表达的变化规律。方法:选择200605/06济南地区部队干休所离休老干部查体人员。代谢综合征及其相关组分诊断标准采用1999年WHO代谢综合征的工作定义。应用Setriscam^TM数字化成像技术及放射免疫分析法,对代谢综合征组90例(其中骨质疏松22例和骨量减少30例),单纯高血压组38例,单纯糖尿病组30例,单纯高血脂组32例患者进行骨密度、骨钙素等骨代谢指标和生化指标的测定,与相同年龄对照组进行比较,并对骨密度与各项骨代谢指标进行相关性分析。结果:①代谢综合征骨质疏松组、代谢综合征骨量减少组、单纯糖尿病组的骨密度和峰值百分比明显低于正常对照组(P〈0.05—0.01)。②代谢综合征组、代谢综合征骨质疏松和骨量减少组骨钙素、Ⅰ型胶原C端肽低于正常对照组(P〈0.05-0.01),甲状旁腺素高于正常对照组(P〈0.05)。三组患者均存在不同程度高血糖、高血压和血脂紊乱。③代谢综合征骨质疏松组骨密度与骨钙素呈正相关关系(r=0.262),与甲状旁腺素呈负相关(r=0.233),与血压呈明显负相关(r=-0.285),与生化指标之间无相关性。结论:代谢综合征骨质疏松患者骨密度与骨钙素、甲状旁腺素、Ⅰ型胶原C端肽、血压之间密切相关。AIM: To observe the change rules of bone mineral density (BMD) and bone metabolic products in aged male patients with metabolic syndrome (MS). METHODS: The retired cadres who underwent physical examination in Cadre Reset Institute of Jinan were selected from May to June 2006. Based on the MS diagnosis criteria in 1999, Setriscam^TM digital image-graph technology and radio-immunoassay were used to measure bone metabolic indexes, such BMD and osteocalcin, and biochemical markers in 90 MS patients, including 22 patients with osteoporosis and 30 patients with decreased bone mass, 38 hypertensive patients, 30 DM patients and 32 hyperlipemia (HP) patients. The results were analyzed and compared with those of the control group. While, the correlation of BMD with each bone metabolic indexes was investigated. RESULTS: ①The BMD and the peak value ratio in the MS with osteoporosis, the decreased bone mass and the only DM groups were significantly decreased as compared with those of the control group (P 〈 0.05 0.01). ②The osteocalcin level and the type Ⅰ collagen carboxyl terminal peptide level in the MS, the MS with osteoporosis and the decreased bone mass groups were also significantly decreased as compared with those in the normal control group (P 〈 0.05-0.01 ). While, the level of parathyroid hormone (PTH) was significantly higher than that in the control group (P 〈 0.05). Hyperglycemia, hypertension and dyslipoidemia were all found in the three experimental groups. ③BMD was positively correlated with osteocalcin in the MS with osteoporosis group (r =0.262), negatively correlated with the increased PTH (r = -0.233) and the blood pressure (r = 0.285) and not correlated with other biological indexes. CONCLUSION: BMD is closely related to osteocalcin, PTH, type Ⅰ collagen carboxyl terminal peptide and blood pressure in osteoporotic patients with MS.
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