Thyroid Function Tests in Children and Adolescents With Trisomy 21: Definition of Syndrome-Specific Reference Ranges

被引:2
|
作者
Cattoni, Alessandro [1 ,2 ]
Molinari, Silvia [1 ]
Capitoli, Giulia [3 ]
Masera, Nicoletta [1 ]
Nicolosi, Maria Laura [1 ]
Barzaghi, Silvia [1 ]
Marziali, Giulia [1 ]
Lazzerotti, Alessandra [1 ]
Gazzarri, Alessandra [1 ]
Vimercati, Chiara [1 ]
Sala, Debora [1 ]
Biondi, Andrea [1 ,2 ]
Galimberti, Stefania [3 ]
Fossati, Chiara [1 ]
机构
[1] Fdn IRCCS San Gerardo Tintori, Pediat, Via Pergolesi 33, I-20900 Monza, MB, Italy
[2] Univ Milano Bicocca, Sch Med & Surg, I-20900 Monza, MB, Italy
[3] Univ Milano Bicocca, B4 Ctr Bioinformat Biostat & Bioimaging, I-20854 Vedano Al Lambro, MB, Italy
关键词
Down syndrome; thyroid function tests; reference values; hypothyroidism; thyroxine; thyrotropin; SUBCLINICAL HYPOTHYROIDISM; DOWN-SYNDROME; DYSFUNCTION;
D O I
10.1210/clinem/dgad333
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context The lack of syndrome-specific reference ranges for thyroid function tests (TFT) among pediatric patients with Down syndrome (DS) results in an overestimation of the occurrence of hypothyroidism in this population. Objective To (a) outline the age-dependent distribution of TFT among pediatric patients with DS; (b) describe the intraindividual variability of TFT over time; and (c) assess the role of elevated thyrotropin (TSH) in predicting the future onset of overt hypothyroidism. Methods In this retrospective, monocentric, observational analysis, we included 548 patients with DS (0-18 years) longitudinally assessed between 1992 and 2022. Exclusion criteria were abnormal thyroid anatomy, treatments affecting TFT, and positive thyroid autoantibodies. Results We determined the age-dependent distribution of TSH, FT3, and FT4 and outlined the relative nomograms for children with DS. Compared with non-syndromic patients, median TSH levels were statistically greater at any age (P < .001). Median FT3 and FT4 levels were statistically lower than controls (P < .001) only in specific age classes (0-11 for FT3, 11-18 years for FT4). TSH levels showed a remarkable fluctuation over time, with a poor (23%-53%) agreement between the TSH centile classes at 2 sequential assessments. Finally, the 75th centile was the threshold above which TSH values predicted future evolution into overt hypothyroidism with the best statistical accuracy, with a satisfactory negative predictive value (0.91), but poor positive predictive value (0.15). Conclusion By longitudinally assessing TFT in a wide pediatric DS population, we outlined the syndrome-specific reference nomograms for TSH, FT3, and FT4 and demonstrated a persistent upward shift of TSH compared to non-syndromic children.
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收藏
页码:2779 / 2788
页数:10
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