甲状腺激素替代治疗对亚临床甲状腺功能减退患者蛋氨酸刺激的同型半胱氨酸水平的影响:一项随机、双盲、安慰剂对照研究。
Effect of thyroid hormone replacement on methionine-stimulated homocysteine levels in patients with subclinical hypothyroidism: a randomized, double-blind, placebo-controlled study.
作者信息
Meek Shon, Smallridge Robert C
机构信息
Division of Endocrinology, Mayo Clinic College of Medicine, Jacksonville, Florida 32224-1865, USA.
出版信息
Endocr Pract. 2006 Sep-Oct;12(5):529-34. doi: 10.4158/EP.12.5.529.
OBJECTIVE
To determine whether treatment of subclinical hypothyroidism with levothyroxine would improve homocysteine metabolism.
METHODS
Twenty-four patients with subclinical hypothyroidism who had thyrotropin (thyroid-stimulating hormone or TSH) levels between 5 and 10 microIU/mL and normal free thyroxine concentrations were recruited from a primary care clinic and were randomized to receive levothyroxine (N = 12) or placebo (N = 12) for a period of 6 months in a double-blind, placebo-controlled study. Homocysteine was measured during fasting and after methionine challenge at the beginning and the end of the study in all patients treated with levothyroxine or placebo.
RESULTS
The 12 patients treated with levothyroxine had normal TSH levels at the end of the study, with a median value of 1.8 microIU/mL. The 12 patients receiving placebo had a median TSH of 6.0 microIU/mL after the 6-month study period. The ratio of fasting homocysteine at 6 months in comparison with baseline was 1.16 (95% confidence interval, 0.90 to 1.63) for the levothyroxine-treated group and 1.00 (0.88 to 1.29) for the placebo group (P = 0.95). The ratio of post-methionine homocysteine at 6 months in comparison with baseline was 1.00 (95% confidence interval, 0.92 to 1.35) for the levothyroxine-treated group and 0.89 (0.68 to 1.05) for the placebo group (P = 0.081).
CONCLUSION
In this study, levothyroxine treatment of patients with subclinical hypothyroidism did not alter homocysteine levels in the fasting or post-methionine states.
目的
确定用左甲状腺素治疗亚临床甲状腺功能减退症是否会改善同型半胱氨酸代谢。
方法
从一家初级保健诊所招募了24例亚临床甲状腺功能减退症患者,其促甲状腺激素(甲状腺刺激激素或TSH)水平在5至10微国际单位/毫升之间且游离甲状腺素浓度正常,在一项双盲、安慰剂对照研究中,将他们随机分为接受左甲状腺素治疗组(N = 12)或安慰剂组(N = 12),为期6个月。在研究开始和结束时,对所有接受左甲状腺素或安慰剂治疗的患者在空腹时以及蛋氨酸激发后测量同型半胱氨酸。
结果
接受左甲状腺素治疗的12例患者在研究结束时TSH水平正常,中位数为1.8微国际单位/毫升。在为期6个月的研究期后,接受安慰剂的12例患者的TSH中位数为6.0微国际单位/毫升。左甲状腺素治疗组6个月时空腹同型半胱氨酸与基线相比的比值为1.16(95%置信区间,0.90至1.63),安慰剂组为1.00(0.88至1.29)(P = 0.95)。左甲状腺素治疗组6个月时蛋氨酸激发后同型半胱氨酸与基线相比的比值为1.00(95%置信区间,0.92至1.35),安慰剂组为0.89(0.68至1.05)(P = 0.081)。
结论
在本研究中,用左甲状腺素治疗亚临床甲状腺功能减退症患者并未改变空腹或蛋氨酸激发后状态下的同型半胱氨酸水平。