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1.
Horm Mol Biol Clin Investig ; 35(1)2018 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-30218603

RESUMO

Background Thyroid dysfunction, predominantly hyperthyroidism, has been previously linked to impaired bone mass density (BMD) and increased risk of fractures. On the other hand, data in the field of hypothyroidism (HT) are missing. The purpose of the present study was to investigate the impact of thyroid disorders on bone density serum and urine calcium (Ca) and phosphate (P) as well as serum osteocalcin and alkaline phosphatase and urine hydroxyproline in a series of post-menopausal women. Materials and methods The study was conducted in the Reproductive Endocrinology Outpatient Clinic of our hospital. A consecutive series of post-menopausal women was included, after excluding patients under hormone treatment (including levothyroxine supplementation) and those who received raloxifene, tamoxifen or tibolone during the study period as well as those who received treatment during the previous 12 months were excluded from the present study. Results Overall, 188 women were included in the present study. Among them, 143 women had normal thyroid function, 32 women had hyperthyroidism and 13 women had HT. Correlation of thyroid function indices with osteoporosis indices revealed statistically significant correlations between thyroxine (T4) and free triiodothyronine (T3) with T-, Z-scores and BMD. Logistic regression analysis concerning the impact of HT and hyperthyroidism on T-score, Z-score and bone mass density revealed that both pathological entities negatively affect bone health (p < 0.05). Conclusion The findings of our study suggest that not only hyperthyroidism, but also HT negatively affects BMD. Future studies should investigate this association and corroborate our findings.


Assuntos
Densidade Óssea , Osso e Ossos/fisiopatologia , Hipertireoidismo/fisiopatologia , Hipotireoidismo/fisiopatologia , Osteoporose/fisiopatologia , Osso e Ossos/metabolismo , Estudos Transversais , Feminino , Humanos , Hipertireoidismo/complicações , Hipertireoidismo/metabolismo , Hipotireoidismo/complicações , Hipotireoidismo/metabolismo , Pessoa de Meia-Idade , Osteoporose/complicações , Osteoporose/metabolismo
2.
Horm Mol Biol Clin Investig ; 33(3)2017 Oct 31.
Artigo em Inglês | MEDLINE | ID: mdl-29087956

RESUMO

Background Obesity and metabolic syndrome (MetS) during the perimenopausal period and in menopause have been linked to altered bone mass density (BMD) in various experimental studies. However, current clinical studies provide conflicting results in this field. The purpose of the present study was to evaluate this association. Materials and methods We conducted a prospective case control study that was based on a consecutive series of menopausal women who attended the Reproductive Endocrinology Outpatient Clinic of our hospital between January 2013 and December 2016. Results One hundred and forty post-menopausal women were included in the present study. After stratifying the women in two groups according to the presence of MetS we observed that bone turnover markers remained unaffected by the presence of MetS (p > 0.05). On the other hand, both the T- and Z-scores of women with MetS were significantly higher compared to healthly postmenopausal women [T-score: 0.4 (-0.7 to 1.3) vs. -1 (-1.62 to -0.1), p < 0.001] [Z-score: 0.55 (-0.3 to 1.7) vs. -0.4 (-1.1 to 0.4), p = 0.003]. Conclusions According to the findings of our study the presence of MetS during the perimenopausal years seems to have a mild benefit on bone mass density. The pathophysiology that underlies this effect remains unclear as bone turnover markers seem to be unaffected by MetS.


Assuntos
Densidade Óssea , Osso e Ossos/metabolismo , Osso e Ossos/patologia , Síndrome Metabólica/metabolismo , Síndrome Metabólica/patologia , Absorciometria de Fóton , Biomarcadores , Pesos e Medidas Corporais , Estudos de Casos e Controles , Estudos Transversais , Feminino , Humanos , Menopausa , Síndrome Metabólica/diagnóstico , Síndrome Metabólica/etiologia , Osteoporose/etiologia , Osteoporose/metabolismo , Osteoporose/patologia , Pacientes Ambulatoriais , Pós-Menopausa
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