TY - JOUR
T1 - Relationships between follicle-stimulating hormone and adiponectin in postmenopausal women
AU - Huang, Wan Yu
AU - Chen, Dar Ren
AU - Kor, Chew Teng
AU - Chen, Ting Yu
AU - Lin, Po Te
AU - Chien Tseng, Joseph Ta
AU - Wu, Hung Ming
N1 - Funding Information:
This study was funded by the MOST 106-2314-B-371-003 grant from the Ministry of Science and Technology Taiwan, and by grants 107-CCH-NPI-052, and 108-CCH-IRP-129 from the Changhua Christian Hospital Research Foundation, Changhua City, Taiwan.
Funding Information:
Funding: This study was funded by the MOST 106-2314-B-371-003 grant from the Ministry of Science and Technology, Taiwan, and by grants 107-CCH-NPI-052, and 108-CCH-IRP-129 from the Changhua Christian Hospital Research Foundation, Changhua City, Taiwan.
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/10
Y1 - 2020/10
N2 - Beyond fertility, follicle-stimulating hormone (FSH) may exert action on adipocytes, which are the major source of adiponectin and leptin, linking to insulin resistance. Therefore, we evaluated the relationships between FSH and adipocyte-derived hormones. This cross-sectional study enrolled postmenopausal women aged 40–65 years. The variables measured in this study included clinical parameters, fasting levels of sex hormones, glucose, insulin, and adipokines. A total of 261 women without breast cancer, 88 women with breast cancer receiving tamoxifen, and 59 women with breast cancer receiving additional gonadotropin-releasing hormone analogs were enrolled in this study. Significant differences in the levels of adiponectin, leptin, and FSH were observed between the non-breast cancer group and the breast cancer groups. Spearman’s rank test revealed significant associations of FSH with either body mass index (BMI) or homeostatic model assessment of insulin resistance (HOMA-IR) values in the non-breast cancer group. After adjusting for BMI, age, andmenopause duration, FSH levels were significantly associated with adiponectin (p < 0.001) and the leptin-to-adiponectin ratio (p = 0.008) in the non-breast cancer group, but they were only significantly associated with adiponectin (p = 0.001) in the breast cancer group receiving tamoxifen. Our data show that FSH levels are independently associated with adiponectin levels in postmenopausal women, suggesting that adiponectin may link FSH to metabolic relationships in postmenopausal female.
AB - Beyond fertility, follicle-stimulating hormone (FSH) may exert action on adipocytes, which are the major source of adiponectin and leptin, linking to insulin resistance. Therefore, we evaluated the relationships between FSH and adipocyte-derived hormones. This cross-sectional study enrolled postmenopausal women aged 40–65 years. The variables measured in this study included clinical parameters, fasting levels of sex hormones, glucose, insulin, and adipokines. A total of 261 women without breast cancer, 88 women with breast cancer receiving tamoxifen, and 59 women with breast cancer receiving additional gonadotropin-releasing hormone analogs were enrolled in this study. Significant differences in the levels of adiponectin, leptin, and FSH were observed between the non-breast cancer group and the breast cancer groups. Spearman’s rank test revealed significant associations of FSH with either body mass index (BMI) or homeostatic model assessment of insulin resistance (HOMA-IR) values in the non-breast cancer group. After adjusting for BMI, age, andmenopause duration, FSH levels were significantly associated with adiponectin (p < 0.001) and the leptin-to-adiponectin ratio (p = 0.008) in the non-breast cancer group, but they were only significantly associated with adiponectin (p = 0.001) in the breast cancer group receiving tamoxifen. Our data show that FSH levels are independently associated with adiponectin levels in postmenopausal women, suggesting that adiponectin may link FSH to metabolic relationships in postmenopausal female.
UR - https://www.scopus.com/pages/publications/85094133352
UR - https://www.scopus.com/pages/publications/85094133352#tab=citedBy
U2 - 10.3390/metabo10100420
DO - 10.3390/metabo10100420
M3 - Article
AN - SCOPUS:85094133352
SN - 2218-1989
VL - 10
SP - 1
EP - 10
JO - Metabolites
JF - Metabolites
IS - 10
M1 - 420
ER -