Department of Pathology, Aga Khan University Hospital Nairobi, Nairobi, Kenya.
BMC Endocr Disord. 2023 May 19;23(1):112. doi: 10.1186/s12902-023-01367-6.
Deriving population specific reference intervals (RIs) or at the very least verifying any RI before adoption is good laboratory practice. Siemens has provided RIs for thyroid stimulating hormone (TSH) and free thyroxine (FT4) determined on their Atellica® IM analyzer for all age groups except the neonatal age group which provides a challenge for laboratories that intend to use it to screen for congenital hypothyroidism (CH) and other thyroid disorders in neonates. We set out to determine RIs for TSH and FT4 using data obtained from neonates undergoing routine screening for CH at the Aga Khan University Hospital, Nairobi, Kenya.
TSH and FT4 data for neonates aged 30 days and below were extracted from the hospital management information system for the period March 2020 to June 2021. A single episode of testing for the same neonate was included provided both TSH and FT4 were done on the same sample. RI determination was performed using a non-parametric approach.
A total of 1243 testing episodes from 1218 neonates had both TSH and FT4 results. A single set of test results from each neonate was used to derive RIs. Both TSH and FT4 declined with increase in age with a more marked decline seen in the first 7 days of life. There was a positive correlation between logFT4 and logTSH (r (1216) = 0.189, p = < 0.001). We derived TSH RIs for the age groups 2-4 days (0.403-7.942 µIU/mL) and 5-7 days (0.418-6.319 µIU/mL), and sex specific RIs for males (0.609-7.557 µIU/mL) and females (0.420-6.189 µIU/mL) aged 8-30 days. For FT4, separate RIs were derived for the age groups 2-4 days (1.19-2.59 ng/dL), 5-7 days (1.21-2.29 ng/dL) and 8-30 days (1.02-2.01 ng/dL).
Our neonatal RIs for TSH and FT4 are different from those published or recommended by Siemens. The RIs will serve as a guide for the interpretation of thyroid function tests in neonates from sub-Saharan Africa where routine screening for congenital hypothyroidism using serum samples is done on the Siemens Atellica® IM analyzer.
为了获得特定人群的参考区间(RI),或者至少在采用之前验证任何 RI,这是良好的实验室实践。西门子已经为他们的 Atellica® IM 分析仪上测定的甲状腺刺激激素(TSH)和游离甲状腺素(FT4)提供了所有年龄段的 RI,但新生儿年龄段除外,这对那些打算使用该仪器筛查新生儿先天性甲状腺功能减退症(CH)和其他甲状腺疾病的实验室来说是一个挑战。我们旨在使用在肯尼亚内罗毕 Aga Khan 大学医院接受 CH 常规筛查的新生儿获得的 TSH 和 FT4 数据来确定 RI。
从 2020 年 3 月至 2021 年 6 月期间,从医院管理信息系统中提取了 30 天及以下的新生儿 TSH 和 FT4 数据。只要同一批样本上同时进行了 TSH 和 FT4 的检测,同一新生儿的单次检测结果都包含在内。RI 确定采用非参数方法进行。
来自 1218 名新生儿的 1243 个检测结果都有 TSH 和 FT4 的结果。从每个新生儿中使用一组检测结果来推导 RI。TSH 和 FT4 随着年龄的增长而降低,在生命的前 7 天内下降更为明显。FT4 和 TSH 之间存在正相关(r(1216)= 0.189,p < 0.001)。我们为 2-4 天(0.403-7.942 μIU/mL)和 5-7 天(0.418-6.319 μIU/mL)年龄组以及 8-30 天男性(0.609-7.557 μIU/mL)和女性(0.420-6.189 μIU/mL)的 TSH 推导了特定性别 RI。对于 FT4,为 2-4 天(1.19-2.59 ng/dL)、5-7 天(1.21-2.29 ng/dL)和 8-30 天(1.02-2.01 ng/dL)年龄组分别推导了单独的 RI。
我们的新生儿 TSH 和 FT4 的 RI 与西门子发表的或推荐的不同。这些 RI 将作为撒哈拉以南非洲地区使用西门子 Atellica® IM 分析仪对血清样本进行先天性甲状腺功能减退症常规筛查时解释甲状腺功能检测结果的指南。