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首页> 外文期刊>British Journal of Obstetrics and Gynaecology >Establishment of reference range for thyroid hormones in normal pregnant Indian women.
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Establishment of reference range for thyroid hormones in normal pregnant Indian women.

机译:建立印度正常孕妇甲状腺激素参考范围。

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BACKGROUND: Interpretation of thyroid function tests during pregnancy needs trimester-related reference intervals from pregnant populations with minimal risk for thyroid dysfunction. While India has become iodine sufficient after two decades of salt iodisation, there is no normative data for thyroid function from healthy pregnant women of this country. AIMS AND OBJECTIVES: To determine trimester-specific reference ranges for free triiodothyronine (FT(3)), free thyroxine (FT(4)) and thyrotropin (TSH) from healthy pregnant Indian women. DESIGN: Cross-sectional study in a reference population of pregnant women. SETTING: Primary care level obstetric department in India. POPULATION: Women with uncomplicated pregnancy in any trimester. METHODS: Five hundred and forty-one apparently healthy pregnant women with uncomplicated single intrauterine gestations reporting to the Armed Forces Clinic in any trimester were consecutively recruited. Clinical examination, thyroid ultrasound for echogenicity and nodularity and estimation of FT(3), FT(4), TSH and antithyroid antibodies (antithyroperoxidase [anti-TPO] and antithyroglobulin [anti-Tg]) using electrochemiluminescence technique were carried out. From this entire sample, a disease- and risk-free reference population was obtained by excluding those with any known factor that could affect thyroid function or those who were being treated for thyroid dysfunction. MAIN OUTCOME MEASURE: None. RESULTS: Of the 541 consecutive pregnant women in different trimesters enrolled for the study, 210 women were excluded. The composition of reference population comprising 331 women was 107 in first trimester, 137 in second trimester and 87 in third trimester. The 5th and 95th percentiles values were used to determine the reference ranges for FT(3), FT(4) and TSH. The trimester-wise values in the first, second and third trimesters were: FT(3) (1.92-5.86, 3.2-5.73 and 3.3-5.18 pM/l), FT(4) (12-19.45, 9.48-19.58 and 11.32-17.7 pM/l) and TSH (0.6-5.0, 0.44-5.78 and 0.74-5.7 iu/ml), respectively. Analysis of mean, median values for FT(3), FT(4) and TSH between each trimester showed no significant difference in FT(3) and TSH values (95% CI). However, FT(4) showed significant variation between trimesters with values decreasing with advancing gestational age (P value: first versus second = 0.015, first versus third = 0.003 and second versus third = not significant). Women with antibody positivity and hypoechogenicity of thyroid gland had significantly higher TSH values when compared with women with antibody negativity and normoechogenicity. CONCLUSIONS: Reference ranges of FT(3), FT(4) and TSH have been established for pregnant Indian women using 5th and 95th percentiles.
机译:背景:妊娠期间甲状腺功能检查的解释需要妊娠人群中与妊娠期相关的参考间隔,而甲状腺功能障碍的风险最小。尽管经过数十年的盐碘化处理,印度的碘已经足够了,但尚无该国健康孕妇甲状腺功能的规范数据。目的和目的:确定来自健康印度孕妇的游离三碘甲状腺素(FT(3)),游离甲状腺素(FT(4))和促甲状腺激素(TSH)的三个月特定参考范围。设计:在参考孕妇群体中进行横断面研究。地点:印度的初级保健产科。人口:任何孕中期妊娠的妇女。方法:连续征集了541名明显健康的孕妇,这些孕妇在任何三个月中都向武装部队诊所报告了简单的单次子宫内妊娠。进行了临床检查,甲状腺超声检查的回声和结节性,并使用电化学发光技术评估了FT(3),FT(4),TSH和抗甲状腺抗体(抗甲状腺素过氧化物酶[anti-TPO]和抗甲状腺球蛋白[anti-Tg])。从整个样本中,通过排除那些可能影响甲状腺功能的已知因素或正在接受甲状腺功能障碍治疗的人群,来获得无疾病和无风险的参考人群。主要观察指标:无。结果:在参加本研究的541名不同孕期连续怀孕的妇女中,有210名妇女被排除在外。包括331名妇女的参考人口的组成在孕中期为107名,在孕中期为137名,在孕晚期为87名。第5个百分点和第95个百分点值用于确定FT(3),FT(4)和TSH的参考范围。妊娠中期,中期和晚期三个月的值分别为:FT(3)(1.92-5.86、3.2-5.73和3.3-5.18 pM / l),FT(4)(12-19.45、9.48-19.58和11.32) -17.7 pM / l)和TSH(0.6-5.0、0.44-5.78和0.74-5.7 iu / ml)。每个孕期之间的FT(3),FT(4)和TSH平均值,中位数分析显示,FT(3)和TSH值(95%CI)没有显着差异。但是,FT(4)显示三个月之间的显着差异,其值随着胎龄的增加而降低(P值:第一对第二= 0.015,第一对第三= 0.003,第二对第三=不显着)。与具有抗体阴性和正常回生性的女性相比,具有抗体阳性和甲状腺功能低下性的女性的TSH值明显更高。结论:FT(3),FT(4)和TSH的参考范围已确定为使用5%和95%百分位数的印度孕妇。

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