Weight loss progresses with the progression of idiopathic pulmonary fibrosis (IPF), and acute exacerbation of IPF (AE-IPF) frequently occurs in its advanced stage. Adiponectin and leptin are adipokines produced from adipose tissue, and are related to thinness and obesity, respectively. Additionally, these adipokines are implicated in the regulation of inflammation and fibrosis centering on peroxisome proliferator-activated receptor γ (PPARγ). However, the relationship between adiponectin/leptin and AE-IPF remains poorly known. We conducted this study to evaluate levels of serum adiponectin/leptin, and to elucidate the clinical importance of adiponectin and leptin in patients with AE-IPF. Thirty-two patients (39 episodes) who were diagnosed with AE-IPF at our hospital from 1997 to 2016 were retrospectively studied. Serum adiponectin and leptin concentrations were measured with enzyme-linked immunosorbent assay. Patients with AE-IPF showed higher levels of serum adiponectin and leptin than those at initial diagnosis of IPF (pâ=â0.007 and pâ=â0.027, respectively). Serum adiponectin/leptin (A/L) ratio was negatively correlated with body mass index at AE-IPF (râ=â-0.456, pâ=â0.003) and PaO(2) before AE-IPF (râ=â-0.498, pâ=â0.034), and positively correlated with C-reactive protein at AE-IPF (râ=â0.316, pâ=â0.049). Patients with higher A/L ratios had worse survival than those with lower A/L ratios (log-rank, pâ=â0.026). Further, in multivariate analysis, serum A/L ratio was a significant prognostic factor in patients with AE-IPF (HR 2.60, pâ=â0.042). In conclusion, the higher adiponectin/leptin ratio may be associated with a poor prognosis in patients with AE-IPF.
Analysis of serum adiponectin and leptin in patients with acute exacerbation of idiopathic pulmonary fibrosis.
对特发性肺纤维化急性加重期患者血清脂联素和瘦素进行分析
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作者:Enomoto Noriyuki, Oyama Yoshiyuki, Yasui Hideki, Karayama Masato, Hozumi Hironao, Suzuki Yuzo, Kono Masato, Furuhashi Kazuki, Fujisawa Tomoyuki, Inui Naoki, Nakamura Yutaro, Suda Takafumi
| 期刊: | Scientific Reports | 影响因子: | 3.900 |
| 时间: | 2019 | 起止号: | 2019 Jul 19; 9(1):10484 |
| doi: | 10.1038/s41598-019-46990-3 | 研究方向: | 其它 |
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