ABSTRACT:
OBJECTIVE The present study aims to evaluate the influence of hormonal levels of
vitamin D, calcitonin, testosterone, estradiol, and parathyroid in patients
with fractures attributed to osteoporosis when compared with young patients
with fractures resulting from high-impact accidents.
METHODS Blood samples were collected from 30 elderly patients with
osteoporosisattributed fractures (T-score ≤-2.5) (osteoporotic
group), and from 30 young patients with fractures resulting from high-impact
accidents (control group). Measurement of 1,25-hydroxyvitamin D (Kit
Diasorin, Saluggia, Italy), calcitonin (Kit Siemens, Tarrytown, NY, USA),
testosterone, estradiol, and parathyroid hormone (Kit Beckman Couter,
Indianapolis, IN, United States) was performed using a chemiluminescence
technique. Data were inserted into a Microsoft Excel (Microsoft Corp.,
Armonk, WA, USA) spreadsheet and analyzed using Statview statistical
software. Results showing non-normal distribution were analyzed with
nonparametric methods. The Mann-Whitney test was applied for group
comparison, and a Spearman test correlated hormonal levels. Statistical
significance was set at p < 0.05. All analyzes
compared gender and subjects with and without osteoporosis.
RESULTS Women with osteoporosis had significantly lower levels of estradiol and
vitamin D (p = 0.047 and p = 0.0275,
respectively). Men with osteoporosis presented significantly higher levels
of parathyroid hormone (p = 0.0065). There was no
significant difference in testosterone and calcitonin levels.
CONCLUSION Osteoporosis patients presented gender-related hormonal differences. Women
had significantly lower levels of estradiol and vitamin D, whereas men had
significantly higher parathyroid hormone levels, apparently impacting the
disease.
Keywords: osteoporosis; hormones; estradiol; calcitonin; parathyroid hormone.
RESUMO:
OBJETIVO Avaliar a influência dos níveis hormonais de vitamina D,
calcitonina, testosterona, estradiol e paratormônio em pacientes com
fratura atribuída a osteoporose, quando comparados com pacientes
jovens que tiveram fraturas decorrentes de acidente de alto impacto.
MÉTODOS Foram coletadas amostras de sangue de 30 pacientes idosos com fratura
atribuída a osteoporose (T-score ≤-2,5) (grupo com
osteoporose) e 30 amostras de sangue de pacientes jovens que sofreram
fraturas decorrentes de acidentes de alto impacto (grupo controle). Foram
realizadas dosagem de 1,25-hidroxivitamina D (Kit Diasorin, Saluggia,
Italy), calcitonina (Kit Siemens, Tarrytown, NY, USA), testosterona,
estradiol e paratormônio (Kit Beckman Couter, Indianapolis, IN,
United States) pela técnica de quimiluminescência. Os dados
foram inseridos em uma planilha de dados no programa Microsoft Excel
(Microsoft Corp., Redmond, WA, EUA) e analisados pelo programa de
estatística Statview. Os resultados que apresentaram
distribuição não normal foram analisados com
métodos não paramétricos. Para análise de
variáveis comparando-se os dois grupos, aplicou-se o teste
Mann-Whitney. Foi utilizado o teste de correlação de Spearman
para a correlacionar os níveis hormonais. Um valor-p >0.05 foi
considerado significante. Todas as análises foram feitas comparando
gênero e grupos de pacientes come sem osteoporose.
RESULTADOS Mulheres com osteoporose apresentam níveis significativamente menores
de estradiol e vitamina D (p = 0.047 e p =
0.0275), respectivamente. Homens com osteoporose demonstraram níveis
significativamente maiores de paratormônio (p =
0.0065). Não houve diferença significativa nos níveis
de testosterona e calcitonina.
CONCLUSÃO Existem diferenças hormonais entre os gêneros na osteoporose.
Em mulheres, níveis significativamente menores de estradiol e
vitamina D e, nos homens, níveis significativamente maiores de
paratormônio, parecem influenciar na doença.
Palavras-chave: osteoporose; hormônios; estradiol; calcitonina; hormônio paratireóideo.
FIGURES
| Citation: Malheiros-Souza D, Gaia LFP, Sousa FFA, Favaro PIF, Rodrigues V, Rodrigues DBR. Evaluation of Hormonal Influence in Patients with Fractures Attributed to Osteoporosis*. 56(06):804. doi:10.1055/s-0041-1726065 |
| Funding Sources The present study was supported by the Universidade de Uberaba, the Universidade Federal do Triângulo Mineiro, and the Centro de Educação Profissional, in addition to having received financial support from Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG, in the Portuguese acronym), from the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES, in the Portuguese acronym), and from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, in the Portuguese acronym). |
|
* Study developed at the Immunology Laboratory, Department of Biological Sciences, Universidade Federal do Triângulo Mineiro, Uberaba, MG, Brazil. |
|
Authors contributions All authors contributed to the conception and design of the study. The study was designed by Rodrigues V. e Rodrigues D. B. R. Gaia, L. F. P., Sousa F. F. A., Favaro, P. I. and Malheiros-Souza D. collected the material, prepared the database, and performed the statistical analyzes. Malheiros-Souza D. and Rodrigues D. B. R. wrote the manuscript and revised it. Rodrigues V. revised the manuscript. |
|
Conflict of Interests The have no conflict of interests to declare. |
| Received: August 05 2020; Accepted: December 01 2020 |
INTRODUCTION
Osteoporosis results from an imbalance in normal bone metabolism between osteoblasts and osteoclasts.1 Osteoclasts seem more active than osteoblasts in bone resorption processes.2,3 Studies indicate that hormones may play an important role in imbalanced bone formation,4 since parathyroid hormone apparently induces osteocytes differentiation into osteoclasts.5 Likewise, hormones such as estradiol and testosterone are supposedly important,6-8 and testos- terone acts by inhibiting osteoblast apoptosis.9 On the other hand, estrogen seems critical to bone remodeling both in males and females, since it apparently stimulates calcitonin release and activates intestinal vitamin D receptors, resulting in endocrine and immune functions during bone metabolism.10,11 Calcitonin and vitamin D help to maintain adequate serum concentrations of calcium to allow normal bone mineralization. In addition, vitamin D is required for bone growth and remodeling by osteoblasts and osteoclasts.12
The increase in life expectancy resulted in a considerable increase in diseases associated with hormonal changes, including osteoporosis, warranting the focus on studies to clarify these interactions.
The present study aims to evaluate the influence of hormonal serum levels of vitamin D, calcitonin, testosterone, estradiol, and parathyroid hormone in patients with fractures attributed to osteoporosis in comparison with young patients with fractures resulting from high-impact accidents.
MATERIALS AND METHODS
The present project was approved by the Ethics Committee under protocol number 51827515.4.0000.5145.
Study Group
Blood samples were collected from 30 elderly patients with fractures attributed to osteoporosis (T-score ≤-2.5) (osteoporotic group), and from 30 young patients with fractures resulting from high-impact accidents (control group).
Patients with other bone conditions, nonosteoporotic fractures, immunosuppression, malignant neoplasms, or liver disorders were excluded from the study, along with those who did not agree to participate in it. Serum collected from these patients was used for hormone measurement.
Blood Collection
Venous blood collection was always performed in the morning, 1 day after the bone reconstruction surgery indicated by the orthopedist. A blood sample was obtained by venipuncture, using three vacuum collection tubes containing a clot activator and separating gel. Thirty minutes after collection, the samples were centrifuged at 5,000 rotations per minute (rpm) for 10 minutes to obtain serum.
Hormonal Analysis
Serum obtained after blood samples centrifuging was sent for hormonal analysis. Measurement of 1,25-hydroxyvitamin D (Kit Diasorin, Saluggia, Italy), calcitonin (Kit Siemens, Tarrytown, NY, USA), testosterone, estradiol, and parathyroid hormone (Kit Beckman Couter, Indianapolis, IN, United States) was performed using a chemiluminescence technique, a chemical reaction that generates luminous energy. Chemiluminescence reagents are transformed into electrically excited intermediate states and release the absorbed energy as light when becoming less excited.
Statistical Analysis
Data were inserted into a Microsoft Excel (Microsoft Corp., Redmond, WA, USA) spreadsheet and analyzed using Statview statistical software. Results showing non-normal distribution were analyzed with nonparametric methods. The Mann-Whitney test was applied for group comparison, and a Spearman test correlated hormonal levels. Statistical significance was set at p < 0.05.
RESULTS
The present study measured hormones in 30 patients with osteoporosis and in 30 control subjects, totaling 60 people. The mean age of the patients was 58.8 ± 22.61 years old, and all analyzes compared gender and subjects with or without osteoporosis. ►Table 1 shows the number of patients and the mean age from each group.
In the control group, serum vitamin D levels were significantly higher in females when compared with males (Mann-Whitney test; p = 0.0169). Comparing both groups (osteoporosis and control subjects), serum vitamin D levels were significantly higher in women from the control group than in women with osteoporosis (p = 0.0275). There was no significant difference between males and females from the osteoporosis group (►Figure 1A).
Significantly higher free testosterone levels were observed in males when compared with females in both the control and osteoporotic groups (Mann-Whitney test;*p = 0.0023 and**p = 0.0046). There was no significant differ- ence in free testosterone levels between males from the control and osteoporotic groups (►Figure 1B).
Estradiol levels were significantly lower in women with osteoporosis compared with those of the control group (Mann-Whitney test; p = 0.047). There was no significant difference in estradiol levels between men and women from the control group and the osteoporotic group (►Figure 1C). Parathyroid hormone levels were significantly higher in men with osteoporosis when compared with the control group (Mann-Whitney test; p = 0.0065). There was no sig- nificant difference between women from the control group and women with osteoporosis. No significant difference was observed in parathyroid hormone levels when comparing males and females with or without osteoporosis (►Figure 1D).
There was no significant difference in calcitonin levels between the control and osteoporotic groups, regardless of gender. In addition, there was no significant difference when comparing men and women from both groups (►Figure 1E).
DISCUSSION
Osteoporosis results from an imbalance of bone remodeling potentially caused by hormonal factors. In addition, more recent studies show that immunological factors also play a role in the pathophysiology of the disease. The present study evaluated hormonal levels in patients with osteoporosis and compared gender-related differences.
Our study revealed significant differences in vitamin D, estradiol, and parathyroid hormone levels. Osteoporotic women and young men had significantly lower levels of vitamin D compared with young women. Studies show that vitamin D deficiency is associated with muscle weakness, bone loss, falls and fractures.13 In linewith theliterature, our data suggest that a decrease in vitamin D in older women may contribute to osteoporosis. The present study also showed that reduced estradiol levels are related to the onset of osteoporosis in women > 60 years old, which is consistent with other works, showing that bone health is inversely related to lower estradiol concentrations.7,8,14 Estradiol deficiency was also linked to osteoporosis in men > 64 years old,15 although this association was not observed here.
| Mean Age (years old) | Number of Patients (n) | Minimal Age (years old) | Maximal Age (years old) | |
|---|---|---|---|---|
| Female control subjects | 39.5 | 08 | 18 | 58 |
| Male control subjects | 39.6 | 22 | 19 | 58 |
| Women with osteoporosis | 80.05 | 18 | 64 | 98 |
| Men with osteoporosis | 74.9 | 12 | 60 | 88 |
| Total | 58.8 | 60 | 18 | 98 |
Bone remodeling is also stimulated by parathyroid hormone. A study with elderly women showed a significant increase in parathyroid hormone levels in women with osteoporosis.16 In the present study, significantly higher levels of parathyroid hormone were found in men with osteoporosis, showing that it contributes to the onset of the disease in men > 60 years old; in contrast, women present no differences in parathyroid hormone levels.
Testosterone was not a limiting factor for the onset of osteoporosis in our patients. This hormone seems to be more related to differences between males and females. However, a study showed that testosterone deficiency in men > 64 years old is associated with rapid bone loss, leading to osteoporosis.15 Even though the literature showed that calcitonin acts by inhibiting bone resorption,17 we found nosignificant differences in calcitonin levels between groups and genders.
CONCLUSION
The present study suggests that women with osteoporosis had significantly lower levels of estradiol and vitamin D compared with young women without the disease, whereas men with osteoporosis had significantly higher levels of parathyroid hormone compared with men without the disease. These findings show the importance of hormones and vitamin D in the development of osteoporosis. Although lower testosterone levels are associated with osteoporosis, our study does not show its impact on the disease, except for a significant gender-related difference, regardless of age and of the presence of osteoporosis.
