PMID- 34646438 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220427 IS - 2042-0188 (Print) IS - 2042-0196 (Electronic) IS - 2042-0188 (Linking) VI - 12 DP - 2021 TI - Alteration of serum neuregulin 4 and neuregulin 1 in gestational diabetes mellitus. PG - 20420188211049614 LID - 10.1177/20420188211049614 [doi] LID - 20420188211049614 AB - CONTEXT: Neuregulin 4 (Nrg4) and neuregulin 1 (Nrg1) have been shown to play vital roles in several disorders of glucose metabolism. The pathophysiological role of Nrg4 and Nrg1 in gestational diabetes mellitus (GDM), however, remains poorly understood. We assessed the clinical relevance of the two cytokines in patients with GDM. METHODS: The study recruited 36 GDM patients and 38 age-matched, gestational age (24-28 weeks of gestation)-matched, and BMI (during pregnancy)-matched controls in this study. Serum Nrg4 and Nrg1 were measured using ELISA. Inflammatory factors such as IL-6, IL-1beta, leptin, TNF-alpha, and monocyte chemotactic protein 1 (MCP-1) were determined via Luminex technique. RESULTS: Serum Nrg4 in GDM patients was significantly lower than that in the controls, while Nrg1 was significantly higher in the GDM group (p < 0.01). Inflammatory factors such as IL-6, leptin, and TNF-alpha were significantly increased in GDM patients, while MCP-1 and IL-1beta were not significantly different between the two groups. In addition, serum Nrg4 was negatively correlated with fasting glucose (r = -0.438, p = 0.008), HOMA-IR (r = -0.364, p = 0.029), IL-6 (r = -0.384, p = 0.021), leptin (r = -0.393, p = 0.018), TNF-alpha (r = -0.346, p = 0.039), and MCP-1 (r = -0.342, p = 0.041), and positively correlated with high-density lipoprotein cholesterol (HDL-C) (r = -0.357, p = 0.033) in GDM group. Serum Nrg1 was positively correlated with BMI (r = 0.452, p = 0.006), fasting glucose (r = 0.424, p = 0.010), HOMA-IR (r = 0.369, p = 0.027), and triglyceride (r = 0.439, p = 0.007). The decrease of Nrg4 and the increase of Nrg1 were significantly related to the increased prevalence of GDM. Finally, ROC curve results indicated that Nrg1 combined with IL-6 and TNF-alpha might be an effective means for GDM screening. CONCLUSIONS: Lower circulating Nrg4 and higher circulating Nrg1 serve risk factors of GDM. Nrg1 combined with IL-6 and TNF-alpha might be a potential tool for GDM screening. CI - (c) The Author(s), 2021. FAU - Zhang, Lei AU - Zhang L AUID- ORCID: 0000-0001-9640-711X AD - Department of Endocrinology and Metabolism, Binzhou Medical University Hospital, Binzhou, China. FAU - Lu, Bi AU - Lu B AD - Department of Rheumatology and Endocrinology, Affiliated Aoyang Hospital of Jiangsu University, Suzhou, China. FAU - Wang, Wenhua AU - Wang W AD - Department of Neurology, Wuhan Fourth Hospital, Pu-Ai Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. FAU - Miao, Shifeng AU - Miao S AD - Department of Cardiology, Affiliated Aoyang Hospital of Jiangsu University, Suzhou, China. FAU - Zhou, Shuru AU - Zhou S AD - Aoyang Cancer Institute, Affiliated Aoyang Hospital of Jiangsu University, Suzhou, China. FAU - Cheng, Xingbo AU - Cheng X AD - Department of Endocrinology and Metabolism, The First Affiliated Hospital of Soochow University, Suzhou, China. FAU - Zhu, Jie AU - Zhu J AD - Department of Cardiology, Affiliated Aoyang Hospital of Jiangsu University, Suzhou, China. FAU - Liu, Changmei AU - Liu C AD - Department of Endocrinology and Metabolism, Binzhou Medical University Hospital, Binzhou 256600, Shandong, China. LA - eng PT - Journal Article DEP - 20211008 PL - United States TA - Ther Adv Endocrinol Metab JT - Therapeutic advances in endocrinology and metabolism JID - 101532143 PMC - PMC8504227 OTO - NOTNLM OT - gestational diabetes mellitus OT - inflammation OT - insulin resistance OT - neuregulin 1 OT - neuregulin 4 OT - obesity COIS- Conflict of interest statement: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. EDAT- 2021/10/15 06:00 MHDA- 2021/10/15 06:01 PMCR- 2021/10/08 CRDT- 2021/10/14 06:36 PHST- 2021/03/02 00:00 [received] PHST- 2021/09/12 00:00 [accepted] PHST- 2021/10/14 06:36 [entrez] PHST- 2021/10/15 06:00 [pubmed] PHST- 2021/10/15 06:01 [medline] PHST- 2021/10/08 00:00 [pmc-release] AID - 10.1177_20420188211049614 [pii] AID - 10.1177/20420188211049614 [doi] PST - epublish SO - Ther Adv Endocrinol Metab. 2021 Oct 8;12:20420188211049614. doi: 10.1177/20420188211049614. eCollection 2021.