Bone mineral density and bone microarchitecture after long-term suppressive levothyroxine treatment of differentiated thyroid carcinoma in young adult patients

被引:27
|
作者
Monteiro de Barros, Graziella Mendonca [1 ]
Madeira, Miguel [1 ]
Vieira Neto, Leonardo [1 ]
Paranhos Neto, Francisco de Paula [1 ]
Carvalho Mendonca, Laura Maria [3 ]
Barbosa Lima, Inaya Correa [4 ]
Corbo, Rossana [1 ,2 ]
Fleiuss Farias, Maria Lucia [1 ]
机构
[1] Univ Fed Rio de Janeiro, Hosp Univ Clementino Fraga Filho, Div Endocrinol, Rio De Janeiro, Brazil
[2] Inst Nacl Canc, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Hosp Univ Clementino Fraga Filho, Div Rheumatol, Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Lab Nucl Instrumentat COPPE, Rio De Janeiro, Brazil
关键词
Osteoporosis; Bone density; Thyroid cancer; POSTMENOPAUSAL WOMEN; COMPUTED-TOMOGRAPHY; CORTICAL BONE; METABOLISM; THERAPY; HYPERTHYROIDISM; MASS; CHILDREN; CANCER;
D O I
10.1007/s00774-015-0680-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone mineral density (BMD) seems not to be decreased in young patients given long-term suppressive doses of levothyroxine (LT4), but information regarding the bone microstructure in these patients is lacking. The aim of this study was to determine whether supraphysiologic doses of LT4, initiated during childhood or adolescence for treatment of differentiated thyroid carcinoma (DTC), have any detrimental effects on bone microarchitecture as evaluated by high-resolution peripheral quantitative computed tomography (HR-pQCT). Seventeen patients (27.3 +/- 7.1 years old) with DTC with subclinical hyperthyroidism since adolescence and 34 healthy volunteers matched for age, sex, and body mass index were studied by dual-energy X-ray absorptiometry (DXA) to determine the areal BMD at the lumbar spine, hip, and proximal third of the radius. Volumetric BMD and structural parameters of the trabecular and cortical bone were assessed by HR-pQCT of the distal radius and distal tibia. DTC patients were given suppressive doses of LT4 starting at a mean age of 12.6 years, and the mean duration of treatment was 14.2 years. In DTC patients, clinical parameters did not correlate with DXA or HR-pQCT parameters. No differences were found between the patients and controls with respect to BMD and Z scores at any site evaluated by DXA, and no differences were found in the bone microstructure parameters evaluated by HR-pQCT. This cross-sectional study suggests that long-standing suppressive therapy with LT4 during the attainment of peak bone mass may have no significant adverse effects on bone density or microarchitecture.
引用
收藏
页码:417 / 421
页数:5
相关论文
共 50 条
  • [1] Bone mineral density and bone microarchitecture after long-term suppressive levothyroxine treatment of differentiated thyroid carcinoma in young adult patients
    Graziella Mendonça Monteiro de Barros
    Miguel Madeira
    Leonardo Vieira Neto
    Francisco de Paula Paranhos Neto
    Laura Maria Carvalho Mendonça
    Inayá Corrêa Barbosa Lima
    Rossana Corbo
    Maria Lucia Fleiuss Farias
    [J]. Journal of Bone and Mineral Metabolism, 2016, 34 : 417 - 421
  • [2] Bone mineral density and bone fracture in male patients receiving long-term suppressive levothyroxine treatment for differentiated thyroid carcinoma
    Jordi L. Reverter
    Eulàlia Colomé
    Susana Holgado
    Eva Aguilera
    Berta Soldevila
    Lourdes Mateo
    Anna Sanmartí
    [J]. Endocrine, 2010, 37 : 467 - 472
  • [3] Bone mineral density and bone fracture in male patients receiving long-term suppressive levothyroxine treatment for differentiated thyroid carcinoma
    Reverter, Jordi L.
    Colome, Eulalia
    Holgado, Susana
    Aguilera, Eva
    Soldevila, Berta
    Mateo, Lourdes
    Sanmarti, Anna
    [J]. ENDOCRINE, 2010, 37 (03) : 467 - 472
  • [4] Effect of Suppressive Levothyroxine Therapy on Bone Mineral Density in Young Patients with Differentiated Thyroid Carcinoma
    Zanella, Andre Borsatto
    Marmitt, Laura
    Fighera, Tayane Muniz
    Scheffel, Rafael Selbach
    Spritzer, Poli Mara
    Dora, Jose Miguel
    Maia, Ana Luiza
    [J]. METABOLITES, 2022, 12 (09)
  • [5] Bone mineral density and bone turnover markers in patients on long-term suppressive levothyroxine therapy for differentiated thyroid cancer
    Lee, Mi Young
    Park, Jae Hyun
    Bae, Keum Seok
    Jee, Yong Gwan
    Ko, An Na
    Han, Yong Jea
    Shin, Jang Yel
    Lim, Jung Soo
    Chung, Choon Hee
    Kang, Seong Joon
    [J]. ANNALS OF SURGICAL TREATMENT AND RESEARCH, 2014, 86 (02) : 55 - 60
  • [6] The long term effect of levothyroxine on bone mineral density in patients with well differentiated thyroid carcinoma after treatment
    Eftekhari, Mohammad
    Asadollahi, Abolfazl
    Beiki, Davood
    Izadyar, Sina
    Gholamrezanezhad, Ali
    Assadi, Majid
    Fard-Esfahani, Armaghan
    Fallahi, Babak
    Takavar, Abbas
    Saghari, Mohsen
    [J]. HELLENIC JOURNAL OF NUCLEAR MEDICINE, 2008, 11 (03): : 160 - 163
  • [7] Bone metabolism in patients with differentiated thyroid carcinoma receiving suppressive levothyroxine treatment
    Mikosch, P
    Obermayer-Pietsch, B
    Jost, R
    Jauk, B
    Gallowitsch, HJ
    Kresnik, E
    Leb, G
    Lind, P
    [J]. THYROID, 2003, 13 (04) : 347 - 356
  • [8] Lack of deleterious effect on bone mineral density of long-term thyroxine suppressive therapy for differentiated thyroid carcinoma
    Reverter, JL
    Holgado, S
    Alonso, N
    Salinas, I
    Granada, ML
    Sanmartí, A
    [J]. ENDOCRINE-RELATED CANCER, 2005, 12 (04) : 973 - 981
  • [9] Bone mineral density in male thyroid carcinoma patients taking suppressive therapy with levothyroxine
    Jurasinovic, Z
    Pavlinovic, Z
    Medvedec, M
    Petrovic, R
    [J]. EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1999, 26 (09): : 1056 - 1056
  • [10] Hip bone mineral density, bone turnover and risk of fracture in patients on long-term suppressive L-thyroxine therapy for differentiated thyroid carcinoma
    Heijckmann, AC
    Huijberts, MSP
    Geusens, P
    de Vries, J
    Menheere, PPCA
    Wolffenbuttel, BHR
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2005, 153 (01) : 23 - 29