Serum Adiponectin, a Novel Biomarker Correlates with Skin Thickness in Systemic Sclerosis.

adiponectin biomarkers skin thickness systemic sclerosis

Journal

Journal of personalized medicine
ISSN: 2075-4426
Titre abrégé: J Pers Med
Pays: Switzerland
ID NLM: 101602269

Informations de publication

Date de publication:
19 Oct 2022
Historique:
received: 12 09 2022
revised: 11 10 2022
accepted: 17 10 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 28 10 2022
Statut: epublish

Résumé

The aim was to evaluate the longitudinal association between basal serum adiponectin and repeated measurements of skin thickness during 12 months of follow-up in systemic sclerosis (SSc) patients. We enrolled SSc patients with disease duration > 2 years in a prospective observational study. Skin thickness was measured at baseline and after 12 months of follow-up with modified Rodnan skin score (mRSS). Baseline serum adiponectin was determined using a commercial ELISA kit. We enrolled 66 female SSc patients (median age 54 years, IQR 42−62 years). The median disease duration was 12 (IQR 8−16) years and median baseline serum adiponectin was 9.8 (IQR 5.6−15.6) mcg/mL. The median mRSS was 10 (IQR 6−18) at baseline and 12 (IQR 7−18) at follow-up. A significant correlation was observed between baseline serum adiponectin and disease duration (r = 0.264, p < 0.05), age (r = 0.515, p < 0.0001), baseline mRSS (r = −0.303, p < 0.05), and mRSS at follow-up (r = −0.322, p < 0.001). In multiple regression analysis, only mRSS at follow-up showed an inverse correlation with baseline serum adiponectin (β = −0.132, p < 0.01). The reduction in serum adiponectin levels is correlated with skin thickness.

Identifiants

pubmed: 36294874
pii: jpm12101737
doi: 10.3390/jpm12101737
pmc: PMC9604668
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Università Cattolica del Sacro Cuore Fondazione Policlinico Universitario "A. Gemelli" IRCCS
ID : part of its programs on promotion and dissemination of scientific research (Linea D1 to MM).

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Auteurs

Giorgia Leodori (G)

Department of Translational and Precision Medicine, Sapienza University of Rome, 00189 Rome, Italy.

Chiara Pellicano (C)

Department of Translational and Precision Medicine, Sapienza University of Rome, 00189 Rome, Italy.

Valerio Basile (V)

Clinical Pathology Unit and Cancer Biobank, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.

Amalia Colalillo (A)

Department of Translational and Precision Medicine, Sapienza University of Rome, 00189 Rome, Italy.

Luca Navarini (L)

Unit of Allergology, Clinical Immunology and Rheumatology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.

Antonietta Gigante (A)

Department of Translational and Precision Medicine, Sapienza University of Rome, 00189 Rome, Italy.

Francesca Gulli (F)

Clinical Biochemistry Laboratory, IRCCS "Bambino Gesù" Children's Hospital, 00165 Rome, Italy.

Mariapaola Marino (M)

Department of Translational Medicine and Surgery, Section of General Pathology, "A. Gemelli" IRCCS, Catholic University of the Sacred Heart, 00168 Rome, Italy.

Umberto Basile (U)

Department of Laboratory and Infectious Disease Sciences, "A. Gemelli" IRCCS, Catholic University of the Sacred Heart, 00168 Rome, Italy.

Edoardo Rosato (E)

Department of Translational and Precision Medicine, Sapienza University of Rome, 00189 Rome, Italy.

Classifications MeSH