Literature DB >> 11838730

Effect of different starting doses of levothyroxine on growth and intellectual outcome at four years of age in congenital hypothyroidism.

Mariacarolina Salerno1, Roberto Militerni, Carmela Bravaccio, Maria Micillo, Donatella Capalbo, Maio Salvatore Di, Alfred Tenore.   

Abstract

To evaluate the effect of different initial levothyroxine (LT4) replacement doses on growth and intellectual outcome in patients with congenital hypothyroidism (CH) detected by neonatal screening program, the longitudinal growth and intelligence quotient (IQ) were assessed and compared at 4 years of age in 83 patients with CH. The patients were divided into three groups according to the initial LT4 dose used: (1) group 1 (n = 42) received the previously recommended dose of 6.0-8.0 microg/kg per day; (2) group 2 (n = 21) received a dose of 8.1-10.0 microg/kg per day; (3) Group 3 (n = 20) a dose of 10.1-15.0 microg/kg per day. The IQ, evaluated by the Wechsler Preschool and Primary Scale of Intelligence test at 4 years of age, was significantly higher in group 3 (IQ 98 +/- 9) compared to group 1 (IQ 88 +/- 13; p < 0.05) but not compared to group 2 (IQ 94 +/- 13). However, the IQs were below the normal range (< 85) in six patients from group 2 (28%), but in none of the patients from group 3 (p = 0.03). Patients from group 3, with severe CH at diagnosis, had an IQ (97 +/- 9) at 4 years of age, which was not different from that of patients from the same group with moderate CH at diagnosis (IQ 99 +/- 9). Similar results were also observed in patients from group 2 however, mean IQ scores in these patients (93 +/- 12) were several points lower than those observed in patients from group 3 (95 +/- 15). After the first month of treatment, optimal serum levels of thyroxine (T4) and free thyroxine (FT4) were achieved in all groups, however, only patients from group 3 were able to normalize thyrotropin (TSH) (group 1, 16.0 +/- 12.0; group 2, 9.2 +/- 10.0; and group 3, 2.4 +/- 3.3 mU/L; p < 0.0001). Twelve patients from group 2 treated with an initial LT4 dose above 9 microg/kg per day were able to normalize TSH levels within the first 3 months of life and this resulted in a better IQ (97 +/- 16) compared to the remaining patients from the same group (IQ 90 +/- 9). In the whole group of 83 patients the IQ at 4 years of age was positively correlated to both initial LT4 dosage (r = 0.27, p < 0.02) and FT4 concentrations after the first month of treatment (r = 0.29, p < 0.02), and negatively correlated to TSH concentrations after the first month of treatment (r = -0.27, p < 0.02). No significant differences were observed in height, weight, head circumference, and bone age maturation among the three groups of patients. No clinical signs or symptoms of overtreatment were observed during follow-up in patients receiving the higher LT4 dosage. Our results indicate that high LT4 starting doses rapidly normalize serum TSH concentrations resulting in an improvement of the IQ at 4 years of age, even in patients with severe CH at diagnosis. Growth and bone age maturation are not affected by such a high dose.

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Year:  2002        PMID: 11838730     DOI: 10.1089/105072502753451968

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  26 in total

Review 1.  Detection and treatment of congenital hypothyroidism.

Authors:  Annette Grüters; Heiko Krude
Journal:  Nat Rev Endocrinol       Date:  2011-10-18       Impact factor: 43.330

2.  Development of a risk prediction model for early discrimination between permanent and transient congenital hypothyroidism.

Authors:  Ladan Mehran; Fereidoun Azizi; Pouria Mousapour; Leila Cheraghi; Shahin Yarahmadi; Golshan Amirshekari; Davood Khalili
Journal:  Endocrine       Date:  2021-02-22       Impact factor: 3.633

3.  Individualized treatment to optimize eventual cognitive outcome in congenital hypothyroidism.

Authors:  Jacoba J Bongers-Schokking; Wilma C M Resing; Wilma Oostdijk; Yolanda B de Rijke; Sabine M P F de Muinck Keizer-Schrama
Journal:  Pediatr Res       Date:  2016-08-05       Impact factor: 3.756

4.  Growth development in children with congenital hypothyroidism: the effect of screening and treatment variables-a comprehensive longitudinal study.

Authors:  Zahra Heidari; Awat Feizi; Mahin Hashemipour; Roya Kelishadi; Massoud Amini
Journal:  Endocrine       Date:  2016-08-01       Impact factor: 3.633

5.  [Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China].

Authors:  Jing-Hui Yang; Jing-Hui Zhang; Yin-Hong Zhang; Xiao-Zhi Xu; Hong Chen; Yuan Li; Yan Jiang; Zheng Wang; Bao-Sheng Zhu; Li Li
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2017-07

6.  Congenital hypothyroidism: no adverse effects of high dose thyroxine treatment on adult memory, attention, and behaviour.

Authors:  B Oerbeck; K Sundet; B F Kase; S Heyerdahl
Journal:  Arch Dis Child       Date:  2005-02       Impact factor: 3.791

7.  Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study.

Authors:  Maurizio Delvecchio; Mariacarolina Salerno; Maria Cristina Vigone; Malgorzata Wasniewska; Pietro Pio Popolo; Rosa Lapolla; Alessandro Mussa; Giulia Maria Tronconi; Ida D'Acunzo; Raffaella Di Mase; Rosa Maria Falcone; Andrea Corrias; Filippo De Luca; Giovanna Weber; Luciano Cavallo; Maria Felicia Faienza
Journal:  Endocrine       Date:  2015-03-12       Impact factor: 3.633

Review 8.  Congenital hypothyroidism.

Authors:  Maynika V Rastogi; Stephen H LaFranchi
Journal:  Orphanet J Rare Dis       Date:  2010-06-10       Impact factor: 4.123

Review 9.  Newborn Screening Guidelines for Congenital Hypothyroidism in India: Recommendations of the Indian Society for Pediatric and Adolescent Endocrinology (ISPAE) - Part II: Imaging, Treatment and Follow-up.

Authors:  S Sudhanshu; I Riaz; R Sharma; M P Desai; R Parikh; V Bhatia
Journal:  Indian J Pediatr       Date:  2018-02-17       Impact factor: 1.967

Review 10.  The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.

Authors:  A Cassio; C Corbetta; I Antonozzi; F Calaciura; U Caruso; G Cesaretti; R Gastaldi; E Medda; F Mosca; E Pasquini; M C Salerno; V Stoppioni; M Tonacchera; G Weber; A Olivieri
Journal:  J Endocrinol Invest       Date:  2013-02-12       Impact factor: 4.256

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