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您所在的位置:首頁 > 學術研究 > Thyroid:高VitD狀態(tài)年輕人會導致血循環(huán)TSH下降

Thyroid:高VitD狀態(tài)年輕人會導致血循環(huán)TSH下降

2013-01-30 11:59 閱讀:2450 來源:CMT 作者:網* 責任編輯:網絡
[導讀] 維生素D作為一種免疫調節(jié)劑,可能影響自身免疫性甲狀腺疾病。既往研究顯示維生素D通過減少促甲狀腺激素(TSH)**的碘攝取和抑制細胞生長直接影響甲狀腺細胞。然而,基于人群的維生素D和TSH的關系尚不清楚。
維生素D作為一種免疫調節(jié)劑,可能影響自身免疫性甲狀腺疾病。既往研究顯示維生素D通過減少促甲狀腺激素(TSH)刺激的碘攝取和抑制細胞生長直接影響甲狀腺細胞。然而,基于人群的維生素D和TSH的關系尚不清楚。
泰國瑪希隆大學Ramathibodi醫(yī)院醫(yī)學部La-or chailurkit教授等人進行了一項研究,該研究結果發(fā)表在2013年1月底23卷《甲狀腺》(Thyroid)雜志上。作者發(fā)現年輕個體高維生素D狀態(tài)與血清TSH水平降低相關。
該研究從泰國第四次國家健康調查樣本中按地區(qū)隨機抽取2582例年齡15–98歲的成年人,平均年齡為55.0±0.4歲。按照試驗設計,男女均等。所有入選個體均測量血清25(OH)D、TSH、TPOAb、TgAb。
研究結果表明,TgAb陽性個體的血清TSH水平較高,而總體25(OH)D水平較低。此外,無論VitD缺乏的切點定在20ng/ml還是30ng/ml,TgAb陽性個體VitD缺乏的患病率顯著高于TPOAb和TgAb陰性的個體,分別為:8.3% vs 5.6%,P<0.05和47.6% vs 42.0%,P<0.05。然而,在校正年齡和性別后,VitD狀態(tài)與TPOAb及TgAb陽性無相關關系。為了探討VitD和年齡對血清TSH的可能影響,根據年齡分為3組展開分析,研究發(fā)現僅在低年齡組個體中,高25(OH)D與低TSH獨立相關。
該研究發(fā)現,年輕個體高VitD狀態(tài)與血循環(huán)TSH降低相關。
High Vitamin D Status in Younger Individuals Is Associated with Low Circulating Thyrotropin
Background: Vitamin D is an immunomodulator and may affect autoimmune thyroid diseases. Vitamin D has also been shown to influence thyrocytes directly by attenuating thyrotropin (TSH)-stimulated iodide uptake and cell growth. However, it is unclear how vitamin D status is related to TSH at the population level. The goal of the present study was to investigate the relationship between vitamin D status and TSH levels according to thyroid autoantibodies in a population-based health survey in Thailand.
Methods: A total of 2582 adults, aged 15–98 years, were randomly selected according to the geographical region from the Thailand 4th National Health Examination Survey sample. By study design, the sexes were equally represented. Serum levels of 25-hydroxyvitamin D [25(OH)D], TSH, the thyroid peroxidase antibody (TPOAb), and the thyroglobulin antibody (TgAb) were measured in all subjects.
Results: The mean age was 55.0±0.4 (SE) years. In subjects positive for serum TgAb, serum TSH levels were higher, whereas total serum 25(OH)D levels were lower. In addition, the prevalence of vitamin D insufficiency in TgAb-positive subjects was significantly higher than that observed in TPOAb- and TgAb-negative subjects, whether based on cutoff values of 20 or 30?ng/mL: 8.3% vs. 5.6%, p<0.05; or 47.6% vs. 42.0%, p<0.05, respectively. However, vitamin D status was not associated with positive TPOAb and/or TgAb after controlling for sex and age. To explore the probable interaction between vitamin D status and age on serum TSH, analyses were performed according to age tertiles; it was found that higher 25(OH)D levels were independently associated with lower TSH, but only in subjects in the lowest age tertile.
Conclusions: This population-based study showed that high vitamin D status in younger individuals is associated with low circulating TSH.

 


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