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C 端骨肽在评估左甲状腺素替代治疗所致骨质流失中的应用价值。

Utility of C-terminal Telopeptide in Evaluating Levothyroxine Replacement Therapy-Induced Bone Loss.

作者信息

Christy Alap L, D'Souza Vivian, Babu Ruby P, Takodara Sohil, Manjrekar Poornima, Hegde Anupama, Rukmini M S

机构信息

Department of Biochemistry, Kasturba Medical College, Manipal University, Mangalore, India.

出版信息

Biomark Insights. 2014 Mar 3;9:1-6. doi: 10.4137/BMI.S13965. eCollection 2014.

Abstract

BACKGROUND

Levothyroxine (LT4) therapy has shown to have effects on bone metabolism though its deleterious effect on bone remodeling is debatable. This study was aimed at assessing the diagnostic utility of the bone remodeling marker C-terminal telopeptide (CTx) in detecting early bone loss.

MATERIALS AND METHODS

In this case-control study, 84 premenopausal women of 30-45 years of age were selected. Out of them, 28 were recently diagnosed of hypothyroidism (not on LT4), 28 were on LT4 replacement therapy (100-200 μg/day) for more than five years, and 28 had euthyroid. Plasma CTx levels were estimated. Bone mineral density (BMD) was measured by quantitative ultrasound (QUS) method. Pearson's coefficient of correlation and ANOVA were used for statistical analysis.

RESULTS

CTx was most elevated in LT4-treated group (0.497 ± 0.209 ng/mL). It showed a significant negative correlation with T-score and Z-score of BMD values. In the treatment group of more than 150 μg/day, CTx showed significantly negative correlation with TSH (r = -0.462, P = 0.047).

CONCLUSION

LT4 therapy induces bone loss in hypothyroid patients. CTx levels can measure such bone loss along with BMD. Regular monitoring of CTx with adjustment in LT4 doses may help delay osteoporosis induced by prolonged LT4 replacement therapy.

摘要

背景

左甲状腺素(LT4)治疗已显示对骨代谢有影响,但其对骨重塑的有害作用仍存在争议。本研究旨在评估骨重塑标志物C末端肽(CTx)在检测早期骨质流失中的诊断效用。

材料与方法

在这项病例对照研究中,选取了84名30 - 45岁的绝经前女性。其中,28名最近被诊断为甲状腺功能减退(未接受LT4治疗),28名接受LT4替代治疗(100 - 200μg/天)超过五年,28名甲状腺功能正常。测定血浆CTx水平。采用定量超声(QUS)法测量骨密度(BMD)。采用Pearson相关系数和方差分析进行统计分析。

结果

CTx在LT4治疗组中升高最为明显(0.497±0.209ng/mL)。它与BMD值的T评分和Z评分呈显著负相关。在每日剂量超过150μg的治疗组中,CTx与促甲状腺激素(TSH)呈显著负相关(r = -0.462,P = 0.047)。

结论

LT4治疗可导致甲状腺功能减退患者骨质流失。CTx水平可与BMD一起衡量这种骨质流失。定期监测CTx并调整LT4剂量可能有助于延缓长期LT4替代治疗引起的骨质疏松。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad84/3948734/2a35e5eda2c3/bmi-9-2014-001f1.jpg

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