Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS

Women with polycystic ovary syndrome (PCOS) have an increased risk of developing type 2 diabetes. FGF19, FGF21 and lipocalin-2 have emerged as important markers of metabolic risk. This study aims to compare the levels of FGF19, FGF21 and lipocalin-2 between subjects with or without PCOS, and to inve...

Full description

Bibliographic Details
Main Authors: Feifei Cheng, Noel Yat Hey Ng, Claudia Ha Ting Tam, Yuying Zhang, Cadmon King Poo Lim, Guozhi Jiang, Alex Chi Wai Ng, Tiffany Tse Ling Yau, Lai Ping Cheung, Aimin Xu, Juliana C N Chan, Ronald C W Ma
Format: Article
Language:English
Published: Bioscientifica 2021-10-01
Series:Endocrine Connections
Subjects:
Online Access:https://ec.bioscientifica.com/view/journals/ec/10/10/EC-21-0082.xml
id doaj-26823229e1c84292b2f28809f7ac16bc
record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Feifei Cheng
Noel Yat Hey Ng
Claudia Ha Ting Tam
Yuying Zhang
Cadmon King Poo Lim
Guozhi Jiang
Alex Chi Wai Ng
Tiffany Tse Ling Yau
Lai Ping Cheung
Aimin Xu
Juliana C N Chan
Ronald C W Ma
spellingShingle Feifei Cheng
Noel Yat Hey Ng
Claudia Ha Ting Tam
Yuying Zhang
Cadmon King Poo Lim
Guozhi Jiang
Alex Chi Wai Ng
Tiffany Tse Ling Yau
Lai Ping Cheung
Aimin Xu
Juliana C N Chan
Ronald C W Ma
Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS
Endocrine Connections
polycystic ovary syndrome
type 2 diabetes
fgf19
fgf21
lipocalin-2
author_facet Feifei Cheng
Noel Yat Hey Ng
Claudia Ha Ting Tam
Yuying Zhang
Cadmon King Poo Lim
Guozhi Jiang
Alex Chi Wai Ng
Tiffany Tse Ling Yau
Lai Ping Cheung
Aimin Xu
Juliana C N Chan
Ronald C W Ma
author_sort Feifei Cheng
title Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS
title_short Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS
title_full Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS
title_fullStr Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS
title_full_unstemmed Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOS
title_sort association between fgf19, fgf21 and lipocalin-2, and diabetes progression in pcos
publisher Bioscientifica
series Endocrine Connections
issn 2049-3614
publishDate 2021-10-01
description Women with polycystic ovary syndrome (PCOS) have an increased risk of developing type 2 diabetes. FGF19, FGF21 and lipocalin-2 have emerged as important markers of metabolic risk. This study aims to compare the levels of FGF19, FGF21 and lipocalin-2 between subjects with or without PCOS, and to investigate the relationship between proteins and diabetes progression. In this nested case–control cohort study, 128 Chinese PCOS women and 128 controls were recruited and followed-up. All subjects underwent the oral glucose tolerance test for the evaluation of glycaemic status. Baseline serum protein levels were measured using ELISA. Compared with controls, PCOS subjects had higher levels of FGF19 (P < 0.001) and FGF21 (P = 0.022), but had lower lipocalin-2 (P < 0.001). In total, 20.8% of PCOS and 9.2% of controls developed diabetes over a mean duration of 10.4 ± 1.2 and 11.3 ± 0.5 years, respectively. Logistic regression analyses suggested FGF19 was positively associated with diabetes progression in controls, after adjusting for age, follow-up duration, waist and fasting glucose (P = 0.026, odds ratio (OR) (95% CI): 7.4 (1.3–43.6)), and the positive relationship between FGF21 and diabetes progression in controls was attenuated by adjusting for age and follow-up duration (P = 0.183). Lipocalin-2 was positively correlated with diabetes progression in PCOS group (P = 0.026, OR (95% CI)): 2.5 (1.1–5.6)); however, this became attenuated after adjusting for waist and fasting glucose (P = 0.081). In conclusion, there is differential expression of FGF1 9, FGF21, and lipocalin-2 in PCOS. The serum level of FGF19, and FGF21 is associated with diabetes progression in women without PCOS, while lipocalin-2 was related to diabetes progression in PCOS women.
topic polycystic ovary syndrome
type 2 diabetes
fgf19
fgf21
lipocalin-2
url https://ec.bioscientifica.com/view/journals/ec/10/10/EC-21-0082.xml
work_keys_str_mv AT feifeicheng associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT noelyatheyng associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT claudiahatingtam associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT yuyingzhang associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT cadmonkingpoolim associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT guozhijiang associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT alexchiwaing associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT tiffanytselingyau associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT laipingcheung associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT aiminxu associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT julianacnchan associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
AT ronaldcwma associationbetweenfgf19fgf21andlipocalin2anddiabetesprogressioninpcos
_version_ 1716843245129957376
spelling doaj-26823229e1c84292b2f28809f7ac16bc2021-10-05T11:15:30ZengBioscientificaEndocrine Connections2049-36142021-10-01101012431252https://doi.org/10.1530/EC-21-0082Association between FGF19, FGF21 and lipocalin-2, and diabetes progression in PCOSFeifei Cheng0Noel Yat Hey Ng1Claudia Ha Ting Tam2Yuying Zhang3Cadmon King Poo Lim4Guozhi Jiang5Alex Chi Wai Ng6Tiffany Tse Ling Yau7Lai Ping Cheung8Aimin Xu9Juliana C N Chan10Ronald C W Ma11Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong KongDepartment of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong KongDepartment of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Hong Kong, Hong Kong Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Hong Kong, Hong Kong Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, Hong Kong Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Hong Kong, Hong Kong Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong KongDepartment of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong KongDepartment of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, Hong KongDepartment of Medicine, Li Ka Shing (LKS) Faculty of Medicine, University of Hong Kong, Hong Kong, Hong Kong; State Key Laboratory of Pharmaceutical Biotechnology, University of Hong Kong, Hong Kong, Hong Kong; Department of Pharmacy and Pharmacology, LKS Faculty of Medicine, University of Hong Kong, Hong Kong, Hong Kong Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Chinese University of Hong Kong-Shanghai Jiao Tong University Joint Research Centre in Diabetes Genomics and Precision Medicine, Hong Kong, Hong Kong Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, Hong Kong; Chinese University of Hong Kong-Shanghai Jiao Tong University Joint Research Centre in Diabetes Genomics and Precision Medicine, Hong Kong, Hong Kong Women with polycystic ovary syndrome (PCOS) have an increased risk of developing type 2 diabetes. FGF19, FGF21 and lipocalin-2 have emerged as important markers of metabolic risk. This study aims to compare the levels of FGF19, FGF21 and lipocalin-2 between subjects with or without PCOS, and to investigate the relationship between proteins and diabetes progression. In this nested case–control cohort study, 128 Chinese PCOS women and 128 controls were recruited and followed-up. All subjects underwent the oral glucose tolerance test for the evaluation of glycaemic status. Baseline serum protein levels were measured using ELISA. Compared with controls, PCOS subjects had higher levels of FGF19 (P < 0.001) and FGF21 (P = 0.022), but had lower lipocalin-2 (P < 0.001). In total, 20.8% of PCOS and 9.2% of controls developed diabetes over a mean duration of 10.4 ± 1.2 and 11.3 ± 0.5 years, respectively. Logistic regression analyses suggested FGF19 was positively associated with diabetes progression in controls, after adjusting for age, follow-up duration, waist and fasting glucose (P = 0.026, odds ratio (OR) (95% CI): 7.4 (1.3–43.6)), and the positive relationship between FGF21 and diabetes progression in controls was attenuated by adjusting for age and follow-up duration (P = 0.183). Lipocalin-2 was positively correlated with diabetes progression in PCOS group (P = 0.026, OR (95% CI)): 2.5 (1.1–5.6)); however, this became attenuated after adjusting for waist and fasting glucose (P = 0.081). In conclusion, there is differential expression of FGF1 9, FGF21, and lipocalin-2 in PCOS. The serum level of FGF19, and FGF21 is associated with diabetes progression in women without PCOS, while lipocalin-2 was related to diabetes progression in PCOS women.https://ec.bioscientifica.com/view/journals/ec/10/10/EC-21-0082.xmlpolycystic ovary syndrometype 2 diabetesfgf19fgf21lipocalin-2