Exploring the Role of Adipose Tissue Dysregulation in Vitiligo Pathogenesis: A Body Composition Analysis

Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains unclear. To investigate the role of adipose tissue in the pathogenesis of vitiligo, 50 patients newly diagnosed with vitiligo and 40 age- and...

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Vydáno v:Acta dermato-venereologica Ročník 104; s. adv41018
Hlavní autoři: Shao, XinYi, Pan, Xingyu, Chen, Tingqiao, Chen, Ziyan, Li, Yuhao, Zhong, Judan, Wang, Ruiyao, Yu, Jun, Chen, Jin, Chen, Yangmei
Médium: Journal Article
Jazyk:angličtina
Vydáno: Sweden MJS Publishing, on behalf of the Society for Publication of Acta Dermato-Venereologica 19.11.2024
Medical Journals Sweden
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ISSN:0001-5555, 1651-2057, 1651-2057
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Abstract Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains unclear. To investigate the role of adipose tissue in the pathogenesis of vitiligo, 50 patients newly diagnosed with vitiligo and 40 age- and sex-matched healthy controls were enrolled, and fat mass and distribution using dual-energy X-ray absorptiometry (DXA) and serum adipokine levels using enzyme-linked immunosorbent assay were assessed. The trunk and whole-body fat mass and the trunk/limb fat mass ratio were significantly higher in patients with vitiligo. Higher leptin and resistin levels and lower adiponectin levels were observed. Positive correlation of the trunk fat mass index with vitiligo area scoring index scores (r = 0.38, p = 0.0071) was found. Additionally, plasma adiponectin levels were negatively correlated with vitiligo disease activity scores (r = –0.307, p < 0.05). Receiver operating characteristic curve analysis showed that the percentage of limb lean tissue mass, trunk/limb fat mass ratio, and serum adipokine levels achieved a high area under the curve score for distinguishing patients with vitiligo from healthy controls. In conclusion, the incidence of central obesity and adipokine dysregulation was higher in patients with vitiligo. The potential role of adipose tissue in the pathogenesis of vitiligo should be emphasized.
AbstractList Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains unclear. To investigate the role of adipose tissue in the pathogenesis of vitiligo, 50 patients newly diagnosed with vitiligo and 40 age- and sex-matched healthy controls were enrolled, and fat mass and distribution using dual-energy X-ray absorptiometry (DXA) and serum adipokine levels using enzyme-linked immunosorbent assay were assessed. The trunk and whole-body fat mass and the trunk/limb fat mass ratio were significantly higher in patients with vitiligo. Higher leptin and resistin levels and lower adiponectin levels were observed. Positive correlation of the trunk fat mass index with vitiligo area scoring index scores (r = 0.38, p = 0.0071) was found. Additionally, plasma adiponectin levels were negatively correlated with vitiligo disease activity scores (r = -0.307, p < 0.05). Receiver operating characteristic curve analysis showed that the percentage of limb lean tissue mass, trunk/limb fat mass ratio, and serum adipokine levels achieved a high area under the curve score for distinguishing patients with vitiligo from healthy controls. In conclusion, the incidence of central obesity and adipokine dysregulation was higher in patients with vitiligo. The potential role of adipose tissue in the pathogenesis of vitiligo should be emphasized.Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains unclear. To investigate the role of adipose tissue in the pathogenesis of vitiligo, 50 patients newly diagnosed with vitiligo and 40 age- and sex-matched healthy controls were enrolled, and fat mass and distribution using dual-energy X-ray absorptiometry (DXA) and serum adipokine levels using enzyme-linked immunosorbent assay were assessed. The trunk and whole-body fat mass and the trunk/limb fat mass ratio were significantly higher in patients with vitiligo. Higher leptin and resistin levels and lower adiponectin levels were observed. Positive correlation of the trunk fat mass index with vitiligo area scoring index scores (r = 0.38, p = 0.0071) was found. Additionally, plasma adiponectin levels were negatively correlated with vitiligo disease activity scores (r = -0.307, p < 0.05). Receiver operating characteristic curve analysis showed that the percentage of limb lean tissue mass, trunk/limb fat mass ratio, and serum adipokine levels achieved a high area under the curve score for distinguishing patients with vitiligo from healthy controls. In conclusion, the incidence of central obesity and adipokine dysregulation was higher in patients with vitiligo. The potential role of adipose tissue in the pathogenesis of vitiligo should be emphasized.
Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains unclear. To investigate the role of adipose tissue in the pathogenesis of vitiligo, 50 patients newly diagnosed with vitiligo and 40 age- and sex-matched healthy controls were enrolled, and fat mass and distribution using dual-energy X-ray absorptiometry (DXA) and serum adipokine levels using enzyme-linked immunosorbent assay were assessed. The trunk and whole-body fat mass and the trunk/limb fat mass ratio were significantly higher in patients with vitiligo. Higher leptin and resistin levels and lower adiponectin levels were observed. Positive correlation of the trunk fat mass index with vitiligo area scoring index scores (r = 0.38, p = 0.0071) was found. Additionally, plasma adiponectin levels were negatively correlated with vitiligo disease activity scores (r = –0.307, p < 0.05). Receiver operating characteristic curve analysis showed that the percentage of limb lean tissue mass, trunk/limb fat mass ratio, and serum adipokine levels achieved a high area under the curve score for distinguishing patients with vitiligo from healthy controls. In conclusion, the incidence of central obesity and adipokine dysregulation was higher in patients with vitiligo. The potential role of adipose tissue in the pathogenesis of vitiligo should be emphasized.
Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains unclear. To investigate the role of adipose tissue in the pathogenesis of vitiligo, 50 patients newly diagnosed with vitiligo and 40 age- and sex-matched healthy controls were enrolled, and fat mass and distribution using dual-energy X-ray absorptiometry (DXA) and serum adipokine levels using enzyme-linked immunosorbent assay were assessed. The trunk and whole-body fat mass and the trunk/limb fat mass ratio were significantly higher in patients with vitiligo. Higher leptin and resistin levels and lower adiponectin levels were observed. Positive correlation of the trunk fat mass index with vitiligo area scoring index scores (r = 0.38, p = 0.0071) was found. Additionally, plasma adiponectin levels were negatively correlated with vitiligo disease activity scores (r = –0.307, p < 0.05). Receiver operating characteristic curve analysis showed that the percentage of limb lean tissue mass, trunk/limb fat mass ratio, and serum adipokine levels achieved a high area under the curve score for distinguishing patients with vitiligo from healthy controls. In conclusion, the incidence of central obesity and adipokine dysregulation was higher in patients with vitiligo. The potential role of adipose tissue in the pathogenesis of vitiligo should be emphasized. Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The association between metabolic disorders and vitiligo has attracted increasing attention. However, the role of adipose tissue in vitiligo remains unclear. To investigate this, this study measured regional and whole-body fat mass and distribution using dual-energy X-ray absorptiometry (DXA) and serum adipokine levels among patients and healthy controls. This study found the incidence of central obesity and adipokine dysregulation was higher in patients with vitiligo. The potential role of adipose tissue in the pathogenesis of vitiligo should be emphasized.
Author Wang, Ruiyao
Chen, Ziyan
Pan, Xingyu
Chen, Tingqiao
Zhong, Judan
Chen, Jin
Shao, XinYi
Chen, Yangmei
Yu, Jun
Li, Yuhao
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Cites_doi 10.1111/pcmr.12774
10.1001/jamadermatol.2021.4724
10.1093/jn/123.suppl_2.438
10.1038/nri2921
10.1111/jdv.19162
10.1016/j.abd.2019.07.006
10.3389/fimmu.2019.02555
10.1016/j.clim.2009.11.008
10.1016/j.jid.2017.04.025
10.3389/fphys.2018.00982
10.1371/journal.pone.0177175
10.1016/j.autrev.2014.07.001
10.1159/000481436
10.1371/journal.pone.0154003
10.1186/1758-5996-5-74
10.3389/fimmu.2019.01507
10.1111/j.1365-4632.2011.05377.x
10.1007/s12035-016-0036-7
10.1016/j.jaad.2016.04.036
10.3389/fimmu.2023.1158883
10.4103/ijd.ijd_27_22
10.1111/jocd.14490
10.7754/Clin.Lab.2020.200120
10.21037/qims.2020.03.02
10.2174/1573397112666161029224953
10.1111/jocd.15446
10.1159/000481882
10.1111/ddg.14717
10.1016/j.jaci.2016.10.013
10.1002/med.21754
10.1016/S0140-6736(14)60763-7
10.1126/science.7678183
10.3389/fimmu.2022.1069196
10.1111/bjd.13432
10.1136/jim-2021-002062
10.1111/eci.12997
10.3945/ajcn.2008.26847
10.3389/fimmu.2022.839167
10.1016/j.jdermsci.2010.06.004
10.1111/j.1365-2133.2007.08068.x
10.1186/1758-5996-4-15
10.1111/j.1468-3083.2011.04392.x
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References 85728
85729
85737
85658
85735
85659
85736
85656
85733
85657
85734
85654
85698
85731
85655
85699
85732
85696
85697
85730
85694
85695
85692
85693
85690
85691
85719
85717
85718
85726
85727
85724
85725
85689
85722
85723
85687
85720
85688
85721
85685
85686
85683
85684
85681
85682
85680
85708
85709
85706
85707
85715
85716
85713
85714
85678
85711
85679
85712
85676
85677
85710
85674
85675
85672
85673
85670
85671
85704
85705
85669
85702
85703
85667
85700
85668
85701
85665
85666
85663
85664
85661
85662
85660
References_xml – ident: 85664
  doi: 10.1111/pcmr.12774
– ident: 85659
  doi: 10.1001/jamadermatol.2021.4724
– ident: 85725
  doi: 10.1093/jn/123.suppl_2.438
– ident: 85712
  doi: 10.1038/nri2921
– ident: 85671
  doi: 10.1111/jdv.19162
– ident: 85673
  doi: 10.1016/j.abd.2019.07.006
– ident: 85733
  doi: 10.3389/fimmu.2019.02555
– ident: 85728
  doi: 10.1016/j.clim.2009.11.008
– ident: 85669
  doi: 10.1016/j.jid.2017.04.025
– ident: 85684
  doi: 10.3389/fphys.2018.00982
– ident: 85726
  doi: 10.1371/journal.pone.0177175
– ident: 85687
  doi: 10.1016/j.autrev.2014.07.001
– ident: 85699
  doi: 10.1159/000481436
– ident: 85710
  doi: 10.1371/journal.pone.0154003
– ident: 85721
  doi: 10.1186/1758-5996-5-74
– ident: 85672
  doi: 10.1016/j.abd.2019.07.006
– ident: 85690
  doi: 10.3389/fimmu.2019.01507
– ident: 85661
  doi: 10.1111/j.1365-4632.2011.05377.x
– ident: 85731
  doi: 10.1007/s12035-016-0036-7
– ident: 85658
  doi: 10.1001/jamadermatol.2021.4724
– ident: 85692
  doi: 10.1016/j.jaad.2016.04.036
– ident: 85660
  doi: 10.1111/j.1365-4632.2011.05377.x
– ident: 85677
  doi: 10.3389/fimmu.2023.1158883
– ident: 85678
  doi: 10.4103/ijd.ijd_27_22
– ident: 85718
  doi: 10.1111/jocd.14490
– ident: 85662
  doi: 10.7754/Clin.Lab.2020.200120
– ident: 85702
  doi: 10.21037/qims.2020.03.02
– ident: 85724
  doi: 10.1093/jn/123.suppl_2.438
– ident: 85696
  doi: 10.2174/1573397112666161029224953
– ident: 85715
  doi: 10.1111/jocd.15446
– ident: 85694
  doi: 10.1159/000481882
– ident: 85716
  doi: 10.1111/ddg.14717
– ident: 85666
  doi: 10.1016/j.jaci.2016.10.013
– ident: 85657
  doi: 10.1002/med.21754
– ident: 85679
  doi: 10.4103/ijd.ijd_27_22
– ident: 85655
  doi: 10.1016/S0140-6736(14)60763-7
– ident: 85654
  doi: 10.1016/S0140-6736(14)60763-7
– ident: 85709
  doi: 10.1126/science.7678183
– ident: 85707
  doi: 10.3389/fimmu.2022.1069196
– ident: 85720
  doi: 10.1186/1758-5996-5-74
– ident: 85704
  doi: 10.1111/bjd.13432
– ident: 85737
  doi: 10.1136/jim-2021-002062
– ident: 85730
  doi: 10.1007/s12035-016-0036-7
– ident: 85703
  doi: 10.21037/qims.2020.03.02
– ident: 85656
  doi: 10.1002/med.21754
– ident: 85683
  doi: 10.1111/eci.12997
– ident: 85691
  doi: 10.3389/fimmu.2019.01507
– ident: 85722
  doi: 10.3945/ajcn.2008.26847
– ident: 85674
  doi: 10.3389/fimmu.2022.839167
– ident: 85735
  doi: 10.1016/j.jdermsci.2010.06.004
– ident: 85689
  doi: 10.1111/j.1365-2133.2007.08068.x
– ident: 85705
  doi: 10.1111/bjd.13432
– ident: 85665
  doi: 10.1111/pcmr.12774
– ident: 85686
  doi: 10.1016/j.autrev.2014.07.001
– ident: 85727
  doi: 10.1371/journal.pone.0177175
– ident: 85723
  doi: 10.3945/ajcn.2008.26847
– ident: 85706
  doi: 10.3389/fimmu.2022.1069196
– ident: 85681
  doi: 10.1186/1758-5996-4-15
– ident: 85701
  doi: 10.1111/j.1468-3083.2011.04392.x
– ident: 85700
  doi: 10.1111/j.1468-3083.2011.04392.x
– ident: 85713
  doi: 10.1038/nri2921
– ident: 85711
  doi: 10.1371/journal.pone.0154003
– ident: 85667
  doi: 10.1016/j.jaci.2016.10.013
– ident: 85736
  doi: 10.1136/jim-2021-002062
– ident: 85695
  doi: 10.1159/000481882
– ident: 85729
  doi: 10.1016/j.clim.2009.11.008
– ident: 85732
  doi: 10.3389/fimmu.2019.02555
– ident: 85717
  doi: 10.1111/ddg.14717
– ident: 85663
  doi: 10.7754/Clin.Lab.2020.200120
– ident: 85698
  doi: 10.1159/000481436
– ident: 85675
  doi: 10.3389/fimmu.2022.839167
– ident: 85734
  doi: 10.1016/j.jdermsci.2010.06.004
– ident: 85688
  doi: 10.1111/j.1365-2133.2007.08068.x
– ident: 85670
  doi: 10.1111/jdv.19162
– ident: 85697
  doi: 10.2174/1573397112666161029224953
– ident: 85668
  doi: 10.1016/j.jid.2017.04.025
– ident: 85719
  doi: 10.1111/jocd.14490
– ident: 85685
  doi: 10.3389/fphys.2018.00982
– ident: 85682
  doi: 10.1111/eci.12997
– ident: 85676
  doi: 10.3389/fimmu.2023.1158883
– ident: 85680
  doi: 10.1186/1758-5996-4-15
– ident: 85693
  doi: 10.1016/j.jaad.2016.04.036
– ident: 85708
  doi: 10.1126/science.7678183
– ident: 85714
  doi: 10.1111/jocd.15446
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Snippet Vitiligo is a commonly acquired pigmentary disease characterized by the progressive destruction of melanocytes. The role of adipose tissue in vitiligo remains...
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StartPage adv41018
SubjectTerms Absorptiometry, Photon
adipokines
Adipokines - blood
Adiponectin - blood
adipose tissue
Adipose Tissue - metabolism
Adiposity
Adult
Biomarkers - blood
Body Composition
body composition analysis
Body Fat Distribution
Case-Control Studies
dual-energy X-ray absorptiometry
Female
Humans
Leptin - blood
Male
Middle Aged
Obesity, Abdominal - physiopathology
Original
Predictive Value of Tests
Resistin - blood
vitiligo
Vitiligo - blood
Vitiligo - physiopathology
Young Adult
Title Exploring the Role of Adipose Tissue Dysregulation in Vitiligo Pathogenesis: A Body Composition Analysis
URI https://www.ncbi.nlm.nih.gov/pubmed/39560432
https://www.proquest.com/docview/3130210126
https://pubmed.ncbi.nlm.nih.gov/PMC11589468
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Volume 104
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