Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma

Detalhes bibliográficos
Autor(a) principal: Zanella, André Borsatto
Data de Publicação: 2022
Outros Autores: Marmitt, Laura, Fighera, Tayane Muniz, Scheffel, Rafael Selbach, Spritzer, Poli Mara, Dora, José Miguel Silva, Maia, Ana Luiza Silva
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/254163
Resumo: Suppressive levothyroxine therapy (sT4) is a cornerstone in the management of differentiated thyroid cancer (DTC). Long-term sT4 may affect bone mineral density (BMD). We evaluated the effect of sT4 on the bone mass of young DTC patients. In this cross-sectional study, BMD was evaluated via dual-energy X-ray absorptiometry in DTC patients younger than 25 years at diagnosis and undergoing sT4 for ≥1 year. The two control groups comprised patients matched for sex, age, and body-mass-index who were thyroidectomized for indications other than DTC and undergoing L-T4-replacement therapy, and healthy individuals with no prior known thyroid disease. Ninety-three participants were included (thirty-one in each group). There were no differences in the mean age, female sex (77.4% in all groups), or BMI between the sT4 group and each control group. The median TSH level was lower (0.4 [0.04–6.5] vs. 2.7 [0.8–8.5] mIU/mL, p = 0.01) and the mean L-T4 mcg/Kg levels were higher (2.4 ± 0.6 vs. 1.6 ± 0.3, p = 0.01) in the sT4 group compared to the L-T4-replacement therapy group. Lumbar spine, femoral neck, and total femur BMD were all similar among the groups. sT4 does not impact BMD in young DTC patients after a median time of suppression of 8 years. These findings may help in the decision-making and risk/benefit evaluation of sT4 for this population.
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spelling Zanella, André BorsattoMarmitt, LauraFighera, Tayane MunizScheffel, Rafael SelbachSpritzer, Poli MaraDora, José Miguel SilvaMaia, Ana Luiza Silva2023-02-07T05:01:31Z20222218-1989http://hdl.handle.net/10183/254163001157891Suppressive levothyroxine therapy (sT4) is a cornerstone in the management of differentiated thyroid cancer (DTC). Long-term sT4 may affect bone mineral density (BMD). We evaluated the effect of sT4 on the bone mass of young DTC patients. In this cross-sectional study, BMD was evaluated via dual-energy X-ray absorptiometry in DTC patients younger than 25 years at diagnosis and undergoing sT4 for ≥1 year. The two control groups comprised patients matched for sex, age, and body-mass-index who were thyroidectomized for indications other than DTC and undergoing L-T4-replacement therapy, and healthy individuals with no prior known thyroid disease. Ninety-three participants were included (thirty-one in each group). There were no differences in the mean age, female sex (77.4% in all groups), or BMI between the sT4 group and each control group. The median TSH level was lower (0.4 [0.04–6.5] vs. 2.7 [0.8–8.5] mIU/mL, p = 0.01) and the mean L-T4 mcg/Kg levels were higher (2.4 ± 0.6 vs. 1.6 ± 0.3, p = 0.01) in the sT4 group compared to the L-T4-replacement therapy group. Lumbar spine, femoral neck, and total femur BMD were all similar among the groups. sT4 does not impact BMD in young DTC patients after a median time of suppression of 8 years. These findings may help in the decision-making and risk/benefit evaluation of sT4 for this population.application/pdfengMetabolites. Basel. Vol. 12, no. 9 (Sept. 2022), 842, 9 p.Neoplasias da glândula tireóideDensidade ósseaTireotropinaTiroxinaDifferentiated thyroid carcinomaPediatric patientsSuppressive levothyroxineBone densityEffect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinomaEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001157891.pdf.txt001157891.pdf.txtExtracted Texttext/plain36356http://www.lume.ufrgs.br/bitstream/10183/254163/2/001157891.pdf.txtbf2e0bb66e802094e0052b9fbf2a107fMD52ORIGINAL001157891.pdfTexto completo (inglês)application/pdf1617764http://www.lume.ufrgs.br/bitstream/10183/254163/1/001157891.pdf83d96ac78881002e4d6bd423c13bbe97MD5110183/2541632023-06-07 03:41:00.983064oai:www.lume.ufrgs.br:10183/254163Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-06-07T06:41Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
title Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
spellingShingle Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
Zanella, André Borsatto
Neoplasias da glândula tireóide
Densidade óssea
Tireotropina
Tiroxina
Differentiated thyroid carcinoma
Pediatric patients
Suppressive levothyroxine
Bone density
title_short Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
title_full Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
title_fullStr Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
title_full_unstemmed Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
title_sort Effect of suppressive levothyroxine therapy on bone mineral density in young patients with differentiated thyroid carcinoma
author Zanella, André Borsatto
author_facet Zanella, André Borsatto
Marmitt, Laura
Fighera, Tayane Muniz
Scheffel, Rafael Selbach
Spritzer, Poli Mara
Dora, José Miguel Silva
Maia, Ana Luiza Silva
author_role author
author2 Marmitt, Laura
Fighera, Tayane Muniz
Scheffel, Rafael Selbach
Spritzer, Poli Mara
Dora, José Miguel Silva
Maia, Ana Luiza Silva
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Zanella, André Borsatto
Marmitt, Laura
Fighera, Tayane Muniz
Scheffel, Rafael Selbach
Spritzer, Poli Mara
Dora, José Miguel Silva
Maia, Ana Luiza Silva
dc.subject.por.fl_str_mv Neoplasias da glândula tireóide
Densidade óssea
Tireotropina
Tiroxina
topic Neoplasias da glândula tireóide
Densidade óssea
Tireotropina
Tiroxina
Differentiated thyroid carcinoma
Pediatric patients
Suppressive levothyroxine
Bone density
dc.subject.eng.fl_str_mv Differentiated thyroid carcinoma
Pediatric patients
Suppressive levothyroxine
Bone density
description Suppressive levothyroxine therapy (sT4) is a cornerstone in the management of differentiated thyroid cancer (DTC). Long-term sT4 may affect bone mineral density (BMD). We evaluated the effect of sT4 on the bone mass of young DTC patients. In this cross-sectional study, BMD was evaluated via dual-energy X-ray absorptiometry in DTC patients younger than 25 years at diagnosis and undergoing sT4 for ≥1 year. The two control groups comprised patients matched for sex, age, and body-mass-index who were thyroidectomized for indications other than DTC and undergoing L-T4-replacement therapy, and healthy individuals with no prior known thyroid disease. Ninety-three participants were included (thirty-one in each group). There were no differences in the mean age, female sex (77.4% in all groups), or BMI between the sT4 group and each control group. The median TSH level was lower (0.4 [0.04–6.5] vs. 2.7 [0.8–8.5] mIU/mL, p = 0.01) and the mean L-T4 mcg/Kg levels were higher (2.4 ± 0.6 vs. 1.6 ± 0.3, p = 0.01) in the sT4 group compared to the L-T4-replacement therapy group. Lumbar spine, femoral neck, and total femur BMD were all similar among the groups. sT4 does not impact BMD in young DTC patients after a median time of suppression of 8 years. These findings may help in the decision-making and risk/benefit evaluation of sT4 for this population.
publishDate 2022
dc.date.issued.fl_str_mv 2022
dc.date.accessioned.fl_str_mv 2023-02-07T05:01:31Z
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dc.identifier.issn.pt_BR.fl_str_mv 2218-1989
dc.identifier.nrb.pt_BR.fl_str_mv 001157891
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dc.relation.ispartof.pt_BR.fl_str_mv Metabolites. Basel. Vol. 12, no. 9 (Sept. 2022), 842, 9 p.
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