open access

Vol 74, No 3 (2023)
Original paper
Submitted: 2022-10-02
Accepted: 2023-03-09
Published online: 2023-05-02
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The association between complement C1q tumour necrosis factor-related protein-1 (CTRP-1) level and metabolic syndrome

Guirong Bai1, Xiaomin Xie1, Huili Liu1, Dan Qiang1, Yanting He1, Li Zhang1, Xiaojuan Zhang1
·
Pubmed: 37155309
·
Endokrynol Pol 2023;74(3):271-276.
Affiliations
  1. Department of Endocrinology, The First People’s Hospital of Yinchuan, Yinchuan, China

open access

Vol 74, No 3 (2023)
Original Paper
Submitted: 2022-10-02
Accepted: 2023-03-09
Published online: 2023-05-02

Abstract

Introduction: Complement C1q tumour necrosis factor-related protein (CTRP-1) is a member of the C1q protein superfamily that plays a role in metabolism. This retrospective study aimed to investigate associations between CTRP-1 and metabolic syndrome (MetS).

Material and methods: This study screened subjects who had undergone regular health examinations at the Physical Examination Centre in the First People’s Hospital of Yinchuan (the Second Affiliated Hospital of Ningxia Medical University) between November 2017 and September 2020. The total recruited population included 430 subjects who had undergone regular health examinations, excluding 112 subjects with high glycated haemoglobin (HbA1c ≥ 7). Finally, the data of 318 participants were further analysed. Non-diabetic subjects were divided into 2 groups: one with MetS and one without MetS (controls). Serum CTRP-1 concentrations were evaluated using an enzyme-linked immunosorbent assay.

Results: A total of 318 subjects were included, among whom 176 were diagnosed with MetS (MetS group) and 142 were not (non-MetS controls). The MetS group had significantly lower CTRP-1 levels than non-MetS controls (128.51 [111.56–143.05] vs. 138.82 [122.83–154.33] ng/mL, p < 0.001). Correlation analysis showed that serum CTRP-1 levels correlated negatively with body mass index (r = –0.161, p = 0.004), waist circumference (r = –0.191, p = 0.001), systolic blood pressure (r = –0.198, p < 0.001), diastolic blood pressure (r = –0.145, p = 0.010), fasting blood glucose (FBG) (r = –0.562, p < 0.001), fasting insulin (FIns) (r = –0.424, p < 0.001), and homeostasis model assessment of insulin resistance (HOMA-IR) (r = –0.541, p < 0.001). Multiple linear regression models showed that CTRP-1 levels were associated with MetS (p < 0.01). The lipid profile area under the curve (AUC) was comparable to those for FBG and FIns, and it was significantly higher than the AUCs for demographic variables.

Conclusions: The results of this study suggest that the serum CTRP-1 level is negatively associated with MetS. CTRP-1 is a potential metabolism-related protein and is likely to be associated with lipid profiles in MetS.

Abstract

Introduction: Complement C1q tumour necrosis factor-related protein (CTRP-1) is a member of the C1q protein superfamily that plays a role in metabolism. This retrospective study aimed to investigate associations between CTRP-1 and metabolic syndrome (MetS).

Material and methods: This study screened subjects who had undergone regular health examinations at the Physical Examination Centre in the First People’s Hospital of Yinchuan (the Second Affiliated Hospital of Ningxia Medical University) between November 2017 and September 2020. The total recruited population included 430 subjects who had undergone regular health examinations, excluding 112 subjects with high glycated haemoglobin (HbA1c ≥ 7). Finally, the data of 318 participants were further analysed. Non-diabetic subjects were divided into 2 groups: one with MetS and one without MetS (controls). Serum CTRP-1 concentrations were evaluated using an enzyme-linked immunosorbent assay.

Results: A total of 318 subjects were included, among whom 176 were diagnosed with MetS (MetS group) and 142 were not (non-MetS controls). The MetS group had significantly lower CTRP-1 levels than non-MetS controls (128.51 [111.56–143.05] vs. 138.82 [122.83–154.33] ng/mL, p < 0.001). Correlation analysis showed that serum CTRP-1 levels correlated negatively with body mass index (r = –0.161, p = 0.004), waist circumference (r = –0.191, p = 0.001), systolic blood pressure (r = –0.198, p < 0.001), diastolic blood pressure (r = –0.145, p = 0.010), fasting blood glucose (FBG) (r = –0.562, p < 0.001), fasting insulin (FIns) (r = –0.424, p < 0.001), and homeostasis model assessment of insulin resistance (HOMA-IR) (r = –0.541, p < 0.001). Multiple linear regression models showed that CTRP-1 levels were associated with MetS (p < 0.01). The lipid profile area under the curve (AUC) was comparable to those for FBG and FIns, and it was significantly higher than the AUCs for demographic variables.

Conclusions: The results of this study suggest that the serum CTRP-1 level is negatively associated with MetS. CTRP-1 is a potential metabolism-related protein and is likely to be associated with lipid profiles in MetS.

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Keywords

CTRP-1; metabolic syndrome; triglyceride; fasting blood glucose; HOMA-IR

About this article
Title

The association between complement C1q tumour necrosis factor-related protein-1 (CTRP-1) level and metabolic syndrome

Journal

Endokrynologia Polska

Issue

Vol 74, No 3 (2023)

Article type

Original paper

Pages

271-276

Published online

2023-05-02

Page views

1651

Article views/downloads

373

DOI

10.5603/EP.a2023.0032

Pubmed

37155309

Bibliographic record

Endokrynol Pol 2023;74(3):271-276.

Keywords

CTRP-1
metabolic syndrome
triglyceride
fasting blood glucose
HOMA-IR

Authors

Guirong Bai
Xiaomin Xie
Huili Liu
Dan Qiang
Yanting He
Li Zhang
Xiaojuan Zhang

References (15)
  1. Seldin MM, Peterson JM, Byerly MS, et al. Myonectin (CTRP15), a novel myokine that links skeletal muscle to systemic lipid homeostasis. J Biol Chem. 2012; 287(15): 11968–11980.
  2. Wong GW, Wang J, Hug C, et al. A family of Acrp30/adiponectin structural and functional paralogs. Proc Natl Acad Sci U S A. 2004; 101(28): 10302–10307.
  3. Seldin MM, Tan SY, Wong GW. Metabolic function of the CTRP family of hormones. Rev Endocr Metab Disord. 2014; 15(2): 111–123.
  4. Xin Y, Lyu X, Wang C, et al. Elevated circulating levels of CTRP1, a novel adipokine, in diabetic patients. Endocr J. 2014; 61(9): 841–847.
  5. Yang Y, Liu Si, Zhang RY, et al. Association Between C1q/TNF-Related Protein-1 Levels in Human Plasma and Epicardial Adipose Tissues and Congestive Heart Failure. Cell Physiol Biochem. 2017; 42(5): 2130–2143.
  6. Lu L, Zhang RY, Wang XQ, et al. C1q/TNF-related protein-1: an adipokine marking and promoting atherosclerosis. Eur Heart J. 2016; 37(22): 1762–1771.
  7. Wong GW, Krawczyk SA, Kitidis-Mitrokostas C, et al. Molecular, biochemical and functional characterizations of C1q/TNF family members: adipose-tissue-selective expression patterns, regulation by PPAR-gamma agonist, cysteine-mediated oligomerizations, combinatorial associations and metabolic functions. Biochem J. 2008; 416(2): 161–177.
  8. Fahed G, Aoun L, Bou Zerdan M, et al. Metabolic Syndrome: Updates on Pathophysiology and Management in 2021. Int J Mol Sci. 2022; 23(2).
  9. Fathi Dizaji B. The investigations of genetic determinants of the metabolic syndrome. Diabetes Metab Syndr. 2018; 12(5): 783–789.
  10. Rodriguez S, Lei X, Petersen PS, et al. Loss of CTRP1 disrupts glucose and lipid homeostasis. Am J Physiol Endocrinol Metab. 2016; 311(4): E678–E697.
  11. Takamiya T, Zaky WR, Edmundowics D, et al. World Health Organization-defined metabolic syndrome is a better predictor of coronary calcium than the adult treatment panel III criteria in American men aged 40-49 years. Diabetes Care. 2004; 27(12): 2977–2979.
  12. Tang Qi, Li X, Song P, et al. Optimal cut-off values for the homeostasis model assessment of insulin resistance (HOMA-IR) and pre-diabetes screening: Developments in research and prospects for the future. Drug Discov Ther. 2015; 9(6): 380–385.
  13. Chalupova L, Zakovska A, Adamcova K. Development of a novel enzyme-linked immunosorbent assay (ELISA) for measurement of serum CTRP1: a pilot study: measurement of serum CTRP1 in healthy donors and patients with metabolic syndrome. Clin Biochem. 2013; 46(1-2): 73–78.
  14. Yuasa D, Ohashi K, Shibata R, et al. C1q/TNF-related protein-1 functions to protect against acute ischemic injury in the heart. FASEB J. 2016; 30(3): 1065–1075.
  15. Shimada H, Noro E, Suzuki S, et al. Effects of Adipocyte-derived Factors on the Adrenal Cortex. Curr Mol Pharmacol. 2020; 13(1): 2–6.

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