Bone changes in pre- and postmenopausal women with thyroid cancer on levothyroxine therapy:: Evolution of axial and appendicular bone mass

被引:33
作者
Jódar, E [1 ]
López, MB [1 ]
García, L [1 ]
Rigopoulou, D [1 ]
Martínez, G [1 ]
Hawkins, F [1 ]
机构
[1] Univ Hosp 12 Octubre, Serv Endocrinol, E-28021 Madrid, Spain
关键词
bone mass; bone metabolism; LT4; treatment; subclinical hyperthyroidism; thyroid cancer;
D O I
10.1007/s001980050069
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effects of suppressive doses of levothyroxine (LT4) on bone mass are controversial. Our aim was to evaluate the effects on axial and appendicular bone mineral density (BMD) and bone metabolism of long-term LT4 suppressive therapy in women by means of cross-sectional and longitudinal studies, and also to assess the potential influence of menopausal status and LT4 dose. Seventy-six women (aged 47 +/- 13 years, 37 pre- and 39 postmenopausal) on suppressive therapy (67 +/- 34 months duration, mean LT4 dose 168 +/- 41 mu g/l day) from our Thyroid Cancer Unit without previous hyperthyroidism or concomitant hypoparathyroidism were studied. Serum TSH, T-3 free T-4, calcium, phosphorus, alkaline phosphatase, BGP, iPTH and urinary calcium (uCA) were measured. BMD was measured by dual-energy X-ray absorptiometry (DXA) at lumbar spine, femoral neck, Ward's triangle, ultradistal and distal third radius and expressed as a Z-score. In a subset of 27 women aged 46 +/- 15 years (14 pre- and 13 postmenopausal) a second densitometry scan was performed 27 +/- 5 months later. Patients on suppressive therapy showed a small reduction in BMD at the distal third radius (Z-score: -0.77 +/- 0.98; 95% confidence interval: -1.11, -0.44) without differences between pre- and postmenopausal women. Significant relations with the regimen of suppressive therapy and bone turnover markers were detected except at the lumbar spine. In the longitudinal study a significant although mild reduction in femoral neck BMD was found that correlated with prior T-3 and iPTH. In conclusion, our data show a small detrimental effect of cautious LT4 suppressive therapy on bone mass assessed by DXA; it remains to be established whether this increases the prevalence of fractures.
引用
收藏
页码:311 / 316
页数:6
相关论文
共 32 条
[11]   BONE-DENSITY AND MINERAL METABOLISM IN THYROIDECTOMIZED PATIENTS TREATED WITH LONG-TERM L-THYROXINE [J].
GIANNINI, S ;
NOBILE, M ;
SARTORI, L ;
BINOTTO, P ;
CIUFFREDA, M ;
GEMO, G ;
PELIZZO, MR ;
DANGELO, A ;
CREPALDI, G .
CLINICAL SCIENCE, 1994, 87 (05) :593-597
[12]   BONE MASS IN TOTALLY THYROIDECTOMIZED PATIENTS - ROLE OF CALCITONIN DEFICIENCY AND EXOGENOUS THYROID-TREATMENT [J].
GONZALEZ, DC ;
MAUTALEN, CA ;
CORREA, PH ;
ELTAMER, E ;
ELTAMER, S .
ACTA ENDOCRINOLOGICA, 1991, 124 (05) :521-525
[13]   SKELETAL INTEGRITY IN PREMENOPAUSAL AND POSTMENOPAUSAL WOMEN RECEIVING LONG-TERM L-THYROXINE THERAPY [J].
GREENSPAN, SL ;
GREENSPAN, FS ;
RESNICK, NM ;
BLOCK, JE ;
FRIEDLANDER, AL ;
GENANT, HK .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 (01) :5-14
[14]  
HANSEN MA, 1990, J NUCL MED, V31, P1156
[15]   SPINAL BONE MASS AFTER LONG-TERM TREATMENT WITH L-THYROXINE IN POSTMENOPAUSAL WOMEN WITH THYROID-CANCER AND CHRONIC LYMPHOCYTIC THYROIDITIS [J].
HAWKINS, F ;
RIGOPOULOU, D ;
PAPAPIETRO, K ;
LOPEZ, MB .
CALCIFIED TISSUE INTERNATIONAL, 1994, 54 (01) :16-19
[16]  
HAWKINS F, 1996, J BONE MINER RES S1, V11, pS487
[17]   THYROXINE SUPPRESSIVE THERAPY DECREASES BONE-MINERAL DENSITY IN POSTMENOPAUSAL WOMEN [J].
KUNG, AWC ;
LORENTZ, T ;
TAM, SCF .
CLINICAL ENDOCRINOLOGY, 1993, 39 (05) :535-540
[18]   CAREFULLY MONITORED LEVOTHYROXINE SUPPRESSIVE THERAPY IS NOT ASSOCIATED WITH BONE LOSS IN PREMENOPAUSAL WOMEN [J].
MARCOCCI, C ;
GOLIA, F ;
BRUNOBOSSIO, G ;
VIGNALI, E ;
PINCHERA, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (04) :818-823
[19]   A LONGITUDINAL ASSESSMENT OF BONE LOSS IN WOMEN WITH LEVOTHYROXINE-SUPPRESSED BENIGN THYROID-DISEASE AND THYROID-CANCER [J].
MCDERMOTT, MT ;
PERLOFF, JJ ;
KIDD, GS .
CALCIFIED TISSUE INTERNATIONAL, 1995, 56 (06) :521-525
[20]  
Meunier PJ, 1972, ORTHOPEDIA CLINICS N, V3, P745