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A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences
OBJECTIVE: Cross-sectional studies have reported that TSH above or close to the upper normal limit correlates with unfavorable metabolic and cardiovascular outcomes. Certain medications impair intestinal absorption of levothyroxine (L-T4), resulting in undertreated hypothyroidism (viz. failure of se...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462542/ https://www.ncbi.nlm.nih.gov/pubmed/31011539 http://dx.doi.org/10.1016/j.jcte.2019.100189 |
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author | Benvenga, Salvatore Pantano, Rachele Saraceno, Giovanna Lipari, Luigi Alibrando, Antonio Inferrera, Santi Pantano, Giuseppe Simone, Giuseppe Tamà, Sebastiano Scoglio, Riccardo Ursino, Maria Giovanna Simone, Carmen Catalano, Antonino Alecci, Umberto |
author_facet | Benvenga, Salvatore Pantano, Rachele Saraceno, Giovanna Lipari, Luigi Alibrando, Antonio Inferrera, Santi Pantano, Giuseppe Simone, Giuseppe Tamà, Sebastiano Scoglio, Riccardo Ursino, Maria Giovanna Simone, Carmen Catalano, Antonino Alecci, Umberto |
author_sort | Benvenga, Salvatore |
collection | PubMed |
description | OBJECTIVE: Cross-sectional studies have reported that TSH above or close to the upper normal limit correlates with unfavorable metabolic and cardiovascular outcomes. Certain medications impair intestinal absorption of levothyroxine (L-T4), resulting in undertreated hypothyroidism (viz. failure of serum TSH to reach target levels, if hypothyroidism is primary). Further to evaluating the magnitude of sub-optimally treated primary hypothyroidism as a result of co-ingestion of those medications, we wished to ascertain whether the above complications would occur during a low number of years under polypharmacy. METHOD: In this retrospective study in collaboration with 8 family physicians, we enrolled adults with primary hypothyroidism under L-T4 therapy that, for 2 years minimum, was not associated with those medications (non-exposure, baseline) and that, for another 2 years minimum, it was (exposure). Outcomes were serum levels and proportions of serum TSH levels >4.12 mU/L, and proportions of complications. Complications were aggravation of pre-existing or de novo onset of any of metabolic syndrome, impaired fasting glycemia (IFG), diabetes mellitus, dyslipidemia, hypertension, coronary heart disease (CHD), cerebrovascular disease (CVD). RESULT: A total of 114 patients were enrolled. Duration of exposure to the interfering medication was 32.1 ± 6.9 months (median 31; range 24–55). Compared with non-exposure, the exposure period resulted in greater TSH levels (2.81 ± 3.62 [median 1.79] vs 1.27 ± 1.34 [median 0.93], P = 2.2 × 10(−20)) and proportions of values >4.12 mU/L (18.5% vs 4.7%, P = 1.2 × 10(−7)). Seventy-six patients (67%) had complications, whose rates of TSH >4.12 mU/L were greater than in the 36 complication-free patients (22% vs 11%, P = 0.018). CONCLUSION: During a median period of 31 months, there are relevant consequences for L-T4 treated adult hypothyroid patients resulting from hyperthyrotropinemia caused by medications impairing L-T4 absorption. This should be taken into account by future guidelines on hypothyroidism management. |
format | Online Article Text |
id | pubmed-6462542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-64625422019-04-22 A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences Benvenga, Salvatore Pantano, Rachele Saraceno, Giovanna Lipari, Luigi Alibrando, Antonio Inferrera, Santi Pantano, Giuseppe Simone, Giuseppe Tamà, Sebastiano Scoglio, Riccardo Ursino, Maria Giovanna Simone, Carmen Catalano, Antonino Alecci, Umberto J Clin Transl Endocrinol Research Paper OBJECTIVE: Cross-sectional studies have reported that TSH above or close to the upper normal limit correlates with unfavorable metabolic and cardiovascular outcomes. Certain medications impair intestinal absorption of levothyroxine (L-T4), resulting in undertreated hypothyroidism (viz. failure of serum TSH to reach target levels, if hypothyroidism is primary). Further to evaluating the magnitude of sub-optimally treated primary hypothyroidism as a result of co-ingestion of those medications, we wished to ascertain whether the above complications would occur during a low number of years under polypharmacy. METHOD: In this retrospective study in collaboration with 8 family physicians, we enrolled adults with primary hypothyroidism under L-T4 therapy that, for 2 years minimum, was not associated with those medications (non-exposure, baseline) and that, for another 2 years minimum, it was (exposure). Outcomes were serum levels and proportions of serum TSH levels >4.12 mU/L, and proportions of complications. Complications were aggravation of pre-existing or de novo onset of any of metabolic syndrome, impaired fasting glycemia (IFG), diabetes mellitus, dyslipidemia, hypertension, coronary heart disease (CHD), cerebrovascular disease (CVD). RESULT: A total of 114 patients were enrolled. Duration of exposure to the interfering medication was 32.1 ± 6.9 months (median 31; range 24–55). Compared with non-exposure, the exposure period resulted in greater TSH levels (2.81 ± 3.62 [median 1.79] vs 1.27 ± 1.34 [median 0.93], P = 2.2 × 10(−20)) and proportions of values >4.12 mU/L (18.5% vs 4.7%, P = 1.2 × 10(−7)). Seventy-six patients (67%) had complications, whose rates of TSH >4.12 mU/L were greater than in the 36 complication-free patients (22% vs 11%, P = 0.018). CONCLUSION: During a median period of 31 months, there are relevant consequences for L-T4 treated adult hypothyroid patients resulting from hyperthyrotropinemia caused by medications impairing L-T4 absorption. This should be taken into account by future guidelines on hypothyroidism management. Elsevier 2019-04-10 /pmc/articles/PMC6462542/ /pubmed/31011539 http://dx.doi.org/10.1016/j.jcte.2019.100189 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Paper Benvenga, Salvatore Pantano, Rachele Saraceno, Giovanna Lipari, Luigi Alibrando, Antonio Inferrera, Santi Pantano, Giuseppe Simone, Giuseppe Tamà, Sebastiano Scoglio, Riccardo Ursino, Maria Giovanna Simone, Carmen Catalano, Antonino Alecci, Umberto A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
title | A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
title_full | A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
title_fullStr | A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
title_full_unstemmed | A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
title_short | A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
title_sort | minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of l-thyroxine, may have metabolic and cardiovascular consequences |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462542/ https://www.ncbi.nlm.nih.gov/pubmed/31011539 http://dx.doi.org/10.1016/j.jcte.2019.100189 |
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