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ORIGINAL RESEARCH article
Front. Neurol.
Sec. Multiple Sclerosis and Neuroimmunology
Volume 16 - 2025 |
doi: 10.3389/fneur.2025.1528376
This article is part of the Research Topic Neuro-Immune Crosstalk in Peripheral Neuropathy: From Mechanisms to Therapeutic Opportunities View all articles
Clinical and biochemical characteristics for patients with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome: a pilot observational study
Provisionally accepted- 1 Department of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China
- 2 Department of Infectious Diseases, Air Force Hospital of Southern Theatre Command, Guangzhou, China
- 3 Department of Hematology, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China
- 4 School of Basic Medicine, Fourth Military Medical University, Xi'an, China
- 5 Department of Nursing Affairs, Tangdu Hospital, Fourth Military Medical University, Xi'an, China
Background: Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is rare life-threatening condition associated with a clonal plasma cell neoplasm. Objective: The aim of this study is to investigate the clinical and biochemical features in patients with POEMS syndrome before and post-therapy. Methods: Characteristics of demographic information, underlying diseases, clinical manifestations, laboratory indicators, and imaging examination were retrospectively collected when diagnosed and post-therapy in the patients POEMS syndrome between 2018 and 2024. Results: Nineteen newly-diagnosed, treatment-naïve patients with POEMS syndrome were enrolled. The diagnosis of POEMS syndrome was re-analyzed and matched the diagnostic criteria updated in 2023. All patients presented the symptoms of polyneuropathy and positive for M-protein. Most patients suffered with hyperpigmentation (n=18), organomegaly (n=18), elevated vascular endothelial growth factor (VEGF) (n=17), extravascular volume overload (n=15), sclerotic bone lesions (n=11), and hypothyroidism (n=10). Serum alanine aminotransferase, aspartate aminotransferase, total bilirubin, total protein, and albumin levels were down-regulated, while uric acid level was up-regulated in patients with POEMS syndrome. Reduced triiodothyronine, thyroxine, free triiodothyronine levels were negatively correlated with urea nitrogen, creatinine, and uric acid levels in patients with POEMS syndrome. VEGF level, which was negatively correlated with Ca2+ level (r=-0.56), was reduced in most patients with POEMS syndrome receiving bortezomib/ixazomib and lenalidomide/thalidomide therapy. Aspartate aminotransferase, total protein, and estimated glomerular filtration rate levels were increased, while creatinine and uric acid levels were reduced post-therapy in patients with POEMS syndrome. Conclusion: Patients with POEMS syndrome had impaired liver and renal function, and effective therapy might partly repair the liver and renal dysfunction.
Keywords: POEMS Syndrome, Clinical Characteristics, Biochemical indicators, diagnosis, therapy
Received: 14 Nov 2024; Accepted: 16 Jan 2025.
Copyright: © 2025 Li, Zhang, Luo, Wang, Li, Cheng, Dang, Chen and Jiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Wei Jiang, Department of Nursing Affairs, Tangdu Hospital, Fourth Military Medical University, Xi'an, China
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