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Identification of Serum Biomarkers and Pathways of Systemic Lupus Erythematosus with Skin Involvement Through GC/MS-Based Metabolomics Analysis

Overview
Publisher Dove Medical Press
Specialty Dermatology
Date 2022 Jan 27
PMID 35082507
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Abstract

Purpose: Skin involvement is the second most common symptom of systemic lupus erythematosus (SLE), and the prevention of skin lesion development might benefit to lessen the system inflammation burden in SLE. However, the mechanisms of skin lesion in SLE remain unclear.

Patients And Methods: Metabolome based on gas chromatography-mass spectrometry (GC-MS) was used for comparison of serum metabolism among 11 SLE patients with skin lesion (SL), 10 SLE patients without skin lesion (SNL), and 16 healthy controls (HC). The analysis of metabolism profiles was through LUG database, Human Metabolome Database (HMDB) as well as Kyoto Encyclopedia of Genes and Genomes (KEGG).

Results: A total of 14 most meaningful metabolites were found in SL patients compared to SNL patients, and 19 metabolic pathways were enriched. Meanwhile, L-alpha-aminobutyric acid, dehydroascorbic acid, glycine, and L-tyrosine achieved an area under receiver-operating characteristic (ROC) curve of 0.8636, 0.8091, 0.7727, and 0.7636, respectively, indicating their diagnostic potential for SL patients. In addition, the combined model of L-alpha-aminobutyric acid and dehydroascorbic acid provided better diagnostic accuracy.

Conclusion: The metabolomic features of SLE patients with skin lesion could be detected by GC/MS assay. Our study tried to provide new insights into the mechanism of SLE skin injury. Further validation of these findings through larger sample size studies may contribute to the use of metabolic profile analysis.

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References
1.
Silverberg J, Silverberg N . Serum homocysteine as a biomarker of vitiligo vulgaris severity: a pilot study. J Am Acad Dermatol. 2011; 64(2):445-7. DOI: 10.1016/j.jaad.2010.08.025. View

2.
Deng G, Liu L, Kyttaris V, Tsokos G . Lupus serum IgG induces skin inflammation through the TNFR1 signaling pathway. J Immunol. 2010; 184(12):7154-61. PMC: 2926650. DOI: 10.4049/jimmunol.0902514. View

3.
Xie Y, Liu B, Wu Z . Increased interleukin-9 levels in skin lesions from cutaneous lupus erythematosus patients may predict the progression to systemic lupus erythematosus. J Dermatol Sci. 2020; 101(1):78-80. DOI: 10.1016/j.jdermsci.2020.10.016. View

4.
Wintergerst E, Maggini S, Hornig D . Immune-enhancing role of vitamin C and zinc and effect on clinical conditions. Ann Nutr Metab. 2005; 50(2):85-94. DOI: 10.1159/000090495. View

5.
Pflegerl P, Vesely P, Hantusch B, Schlederer M, Zenz R, Janig E . Epidermal loss of JunB leads to a SLE phenotype due to hyper IL-6 signaling. Proc Natl Acad Sci U S A. 2009; 106(48):20423-8. PMC: 2787143. DOI: 10.1073/pnas.0910371106. View