TY - JOUR
T1 - Serum omentin levels
T2 - A possible contribution to vascular involvement in patients with systemic sclerosis
AU - Miura, Shunsuke
AU - Asano, Yoshihide
AU - Saigusa, Ryosuke
AU - Yamashita, Takashi
AU - Taniguchi, Takashi
AU - Takahashi, Takehiro
AU - Ichimura, Yohei
AU - Toyama, Tetsuo
AU - Tamaki, Zenshiro
AU - Tada, Yayoi
AU - Sugaya, Makoto
AU - Sato, Shinichi
AU - Kadono, Takafumi
N1 - Publisher Copyright:
© 2015 Japanese Dermatological Association.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Adipokines have been shown to be potentially involved in various pathological processes of systemic sclerosis (SSc), including inflammation, vasculopathy and fibrosis, through their pleiotropic effects. Omentin is a member of the adipokines, and has a protective effect against vascular inflammation and pathological remodeling leading to atherosclerosis as well as a vasodilatory effect. To assess the potential role of omentin in the development of SSc, we determined serum omentin levels by enzyme-linked immunosorbent assay in 66 SSc and 21 control subjects and evaluated their clinical correlation. Serum omentin levels were significantly decreased in diffuse cutaneous SSc patients compared with limited cutaneous SSc patients, while comparable between total SSc patients and healthy controls. In diffuse cutaneous (dc)SSc, patients with a disease duration of 5 years or less had serum omentin levels significantly lower than those with a disease duration of more than 5 years. In total SSc, serum omentin levels were significantly higher in patients with elevated right ventricular systolic pressure than in the others, while serum omentin levels did not correlate with fibrotic and systemic inflammatory parameters. These results suggest that a loss of omentin-dependent protection against vascular inflammation and remodeling may be related to pathological vascular events of early dcSSc. The elevation of serum omentin levels may serve as a marker of vascular involvement leading to pulmonary arterial hypertension in SSc, which is possibly due to the compensatory induction of omentin against the increased pulmonary vascular tone.
AB - Adipokines have been shown to be potentially involved in various pathological processes of systemic sclerosis (SSc), including inflammation, vasculopathy and fibrosis, through their pleiotropic effects. Omentin is a member of the adipokines, and has a protective effect against vascular inflammation and pathological remodeling leading to atherosclerosis as well as a vasodilatory effect. To assess the potential role of omentin in the development of SSc, we determined serum omentin levels by enzyme-linked immunosorbent assay in 66 SSc and 21 control subjects and evaluated their clinical correlation. Serum omentin levels were significantly decreased in diffuse cutaneous SSc patients compared with limited cutaneous SSc patients, while comparable between total SSc patients and healthy controls. In diffuse cutaneous (dc)SSc, patients with a disease duration of 5 years or less had serum omentin levels significantly lower than those with a disease duration of more than 5 years. In total SSc, serum omentin levels were significantly higher in patients with elevated right ventricular systolic pressure than in the others, while serum omentin levels did not correlate with fibrotic and systemic inflammatory parameters. These results suggest that a loss of omentin-dependent protection against vascular inflammation and remodeling may be related to pathological vascular events of early dcSSc. The elevation of serum omentin levels may serve as a marker of vascular involvement leading to pulmonary arterial hypertension in SSc, which is possibly due to the compensatory induction of omentin against the increased pulmonary vascular tone.
KW - omentin
KW - pulmonary arterial hypertension
KW - systemic sclerosis
KW - vascular inflammation
KW - vasodilation
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U2 - 10.1111/1346-8138.12824
DO - 10.1111/1346-8138.12824
M3 - Article
C2 - 25766303
AN - SCOPUS:84928367977
SN - 0385-2407
VL - 42
SP - 461
EP - 466
JO - Journal of Dermatology
JF - Journal of Dermatology
IS - 5
ER -