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Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study.

Authors :
van Geest FS
Groeneweg S
van den Akker ELT
Bacos I
Barca D
van den Berg SAA
Bertini E
Brunner D
Brunetti-Pierri N
Cappa M
Cappuccio G
Chatterjee K
Chesover AD
Christian P
Coutant R
Craiu D
Crock P
Dewey C
Dica A
Dimitri P
Dubey R
Enderli A
Fairchild J
Gallichan J
Garibaldi LR
George B
Hackenberg A
Heinrich B
Huynh T
Kłosowska A
Lawson-Yuen A
Linder-Lucht M
Lyons G
Monti Lora F
Moran C
Müller KE
Paone L
Paul PG
Polak M
Porta F
Reinauer C
de Rijke YB
Seckold R
Menevşe TS
Simm P
Simon A
Spada M
Stoupa A
Szeifert L
Tonduti D
van Toor H
Turan S
Vanderniet J
de Waart M
van der Wal R
van der Walt A
van Wermeskerken AM
Wierzba J
Zibordi F
Zung A
Peeters RP
Visser WE
Source :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2022 Feb 17; Vol. 107 (3), pp. e1136-e1147.
Publication Year :
2022

Abstract

Context: Patients with mutations in thyroid hormone transporter MCT8 have developmental delay and chronic thyrotoxicosis associated with being underweight and having cardiovascular dysfunction.<br />Objective: Our previous trial showed improvement of key clinical and biochemical features during 1-year treatment with the T3 analogue Triac, but long-term follow-up data are needed.<br />Methods: In this real-life retrospective cohort study, we investigated the efficacy of Triac in MCT8-deficient patients in 33 sites. The primary endpoint was change in serum T3 concentrations from baseline to last available measurement. Secondary endpoints were changes in other thyroid parameters, anthropometric parameters, heart rate, and biochemical markers of thyroid hormone action.<br />Results: From October 15, 2014 to January 1, 2021, 67 patients (median baseline age 4.6 years; range, 0.5-66) were treated up to 6 years (median 2.2 years; range, 0.2-6.2). Mean T3 concentrations decreased from 4.58 (SD 1.11) to 1.66 (0.69) nmol/L (mean decrease 2.92 nmol/L; 95% CI, 2.61-3.23; P < 0.0001; target 1.4-2.5 nmol/L). Body-weight-for-age exceeded that of untreated historical controls (mean difference 0.72 SD; 95% CI, 0.36-1.09; P = 0.0002). Heart-rate-for-age decreased (mean difference 0.64 SD; 95% CI, 0.29-0.98; P = 0.0005). SHBG concentrations decreased from 245 (99) to 209 (92) nmol/L (mean decrease 36 nmol/L; 95% CI, 16-57; P = 0.0008). Mean creatinine concentrations increased from 32 (11) to 39 (13) µmol/L (mean increase 7 µmol/L; 95% CI, 6-9; P < 0.0001). Mean creatine kinase concentrations did not significantly change. No drug-related severe adverse events were reported.<br />Conclusions: Key features were sustainably alleviated in patients with MCT8 deficiency across all ages, highlighting the real-life potential of Triac for MCT8 deficiency.<br /> (© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society.)

Details

Language :
English
ISSN :
1945-7197
Volume :
107
Issue :
3
Database :
MEDLINE
Journal :
The Journal of clinical endocrinology and metabolism
Publication Type :
Academic Journal
Accession number :
34679181
Full Text :
https://doi.org/10.1210/clinem/dgab750