Evidence map›Paper›PMID 39449862›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2024

Type 2 Diabetes Mellitus Aggravates Complement Dysregulation and Affects Cortisol Response in Patients with Post-COVID-19.

Wenrui Ji, Xiaomin Xie, Guirong Bai, Yalei Fan, Yanting He, Li Zhang, Haiyan Zhou, Ling Li, Dan Qiang, Huan Li

Abstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Wenrui Ji *Department of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Xiaomin Xie *Department of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.ORCID 0000-0002-6030-7915
Guirong BaiDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Yalei FanThe Second Clinical Medical School of Ningxia Medical University, Yinchuan, 750001, People's Republic of China.
Yanting HeDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Li ZhangDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Haiyan ZhouDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Ling LiDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Dan QiangDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Huan LiDepartment of Endocrinology, the First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: COVID-19 viral infection results in dysregulation of the complement system and a decrease in cortisol and adrenocorticotropin hormone (ACTH) levels. This study aimed to explore the complement system, as well as cortisol and ACTH responses in patients with post-COVID-19 conditions (PCC) and type 2 diabetes mellitus (T2DM). Patients and Methods: This study recruited 31 patients with PCC and T2DM (PCC-T2DM), 19 patients with PCC (PCC), 10 patients with T2DM (T2DM), and 10 healthy participants (control). Cortisol and ACTH in the PCC and PCC-T2DM groups were assessed using the insulin tolerance test. In the fasting state, serum samples were collected for proteomic analyses. Spearman correlation analysis was performed between proteins and cortisol, as well as between proteins and ACTH. Results: Cortisol and ACTH levels were consistently decreased in the PCC and PCC-T2DM groups. Proteomic analyses revealed that most of the differentially abundant proteins (DAPs) in the PCC vs control and PCC-T2DM vs T2DM were involved in the coagulation and complement cascade, and the essential complement C3 was significantly upregulated in the PCC and PCC-T2DM groups when compared to their controls. Additionally, complement-related DAPs in the PCC vs control and PCC-T2DM vs T2DM were significantly correlated with cortisol and ACTH levels. In comparing PCC-T2DM samples with PCC samples, we found that upregulated DAPs were linked to the complement system and other immune system, and most DAPs were negatively correlated with cortisol and ACTH. Conclusion: Our study revealed that T2DM exacerbated dysregulation of the complement system in patients with PCC, and significant correlations were present between complement protein levels and those of cortisol and ACTH. These results provide novel insights into the dysregulation of complement and endocrine hormones in patients with PCC and T2DM.

Indexed as

adrenocorticotropin hormonecomplementcortisolpost-COVID-19 conditiontype 2 diabetes mellitus

Identifiers

PMID39449862
PMCPMC11499617

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.