首页> 外文学位 >Changes in bone mineral density in men with prostate cancer during treatment with luteinizing hormone-releasing hormone (LHRH) agonist monotherapy.
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Changes in bone mineral density in men with prostate cancer during treatment with luteinizing hormone-releasing hormone (LHRH) agonist monotherapy.

机译:黄体激素释放激素(LHRH)激动剂单药治疗期间前列腺癌男性的骨矿物质密度变化。

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摘要

Studies conducted on men with metastatic prostate cancer have shown that hypogonadism from orchiectomy and luteinizing hormone-releasing hormone (LHRH) agonist therapy resulted in significant decrease in bone mineral density (BMD). The purpose of this study is to compare changes in BMD levels in men who are receiving LHRH agonist monotherapy (LHRH group) than those who are on watchful waiting (WW group) for their non-metastatic prostate cancer over a six-month period.; A prospective, quasi-experimental design was used. Lumbar spine and proximal femur BMD studies were performed using dual energy x-ray absorptiomentry (DEXA) in 18 men on the LHRH group and 16 men on WW group at baseline and at 6 months. Demographic (age, ethnicity), health status (comorbidity, body mass index (BMI)), lifestyle (smoking, alcohol consumption, physical activity, dietary calcium) and disease variables (Gleason score, clinical stage, and PSA) were obtained. Univariate and multivariate analyses were used to identify relationships between demographic, health status, lifestyle, and disease variables and BMD in the spine and femur. T-test was used to compare percent change in BMD over 6-month period between the two groups.; At baseline, 73.5% had osteopenia (55.9%) or osteoporosis (17.6%) of the lumbar spine and/or femur. After 6 months, there was a statistically significant decline in BMD at the lumbar spine in the LHRH group as compared to the WW group (p ≤ 0.05). BMD decreased in the trochanter of the hip of the LHRH group, but did not reach statistical significance (p = 0.10). No significant differences in the incidence of osteopenia and osteoporosis between the two groups at baseline and at 6 months. Aging, low BMI, and elevated PSA were significantly correlated with bone loss in the spine and femur at baseline.; Based on the findings of our study, it may be a reasonable strategy to perform baseline and serial bone densitometry in men with prostate cancer, especially those over 70 years old and have slender stature. Early initiation of pharmacological agents and nursing interventions, such as the exercise and use of calcium and vitamin supplements, may be needed to prevent further progression of bone loss.
机译:对患有转移性前列腺癌的男性进行的研究表明,睾丸切除术和促黄体激素释放激素(LHRH)激动剂治疗导致的性腺功能低下导致骨矿物质密度(BMD)显着降低。这项研究的目的是比较接受LHRH激动剂单一疗法(LHRH组)的男性与六个月内因非转移性前列腺癌而等待观察(WW组)的男性BMD水平的变化。使用了前瞻性的准实验设计。腰椎和股骨近端BMD研究在基线和6个月时对LHRH组的18名男性和WW组的16名男性使用双能X线吸收术(DEXA)进行。获得了人口统计学(年龄,种族),健康状况(合并症,体重指数(BMI)),生活方式(吸烟,饮酒,体育锻炼,饮食中的钙)和疾病变量(格里森评分,临床分期和PSA)。单因素和多因素分析用于确定人口,健康状况,生活方式和疾病变量与脊柱和股骨BMD之间的关系。使用T检验比较两组之间6个月内BMD的变化百分比。在基线时,腰椎和/或股骨的骨质疏松症(55.9%)或骨质疏松症(17.6%)占73.5%。 6个月后,与WW组相比,LHRH组腰椎的BMD有统计学意义的下降(p≤0.05)。 LHRH组的大转子中的BMD下降,但未达到统计学显着性(p = 0.10)。两组在基线和6个月时骨质减少和骨质疏松的发生率无显着差异。基线时,衰老,低BMI和PSA升高与脊柱和股骨的骨丢失显着相关。根据我们的研究结果,对患有前列腺癌的男性,尤其是70岁以上且身材苗条的男性,进行基线和连续骨密度测定可能是一种合理的策略。为防止骨质流失的进一步发展,可能需要及早开始使用药理学药物和护理干预措施,例如锻炼和使用钙和维生素补充剂。

著录项

  • 作者单位

    University of California, Los Angeles.;

  • 授予单位 University of California, Los Angeles.;
  • 学科 Health Sciences Nursing.; Health Sciences Oncology.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 155 p.
  • 总页数 155
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 预防医学、卫生学;肿瘤学;
  • 关键词

  • 入库时间 2022-08-17 11:44:46

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