Key result
Elevated plasma TIMP-1 was identified as an independent risk factor for the diagnosis of pulmonary hypertension among patients with chronic obstructive pulmonary disease (OR 1.258).
Why the study?
Pulmonary hypertension commonly complicates COPD and increases mortality, but blood biomarkers to identify PH in COPD are lacking.
Does elevated circulating TIMP-1 identify pulmonary hypertension in patients with chronic obstructive pulmonary disease?
Case-Control (n=54)
No
Does elevated circulating TIMP-1 identify pulmonary hypertension in patients with chronic obstructive pulmonary disease?
Elevated circulating TIMP-1 levels can serve as a non-invasive diagnostic biomarker for pulmonary hypertension in patients with COPD.
Elevated TIMP-1 should not yet change COPD-PH evaluation; leaves open its diagnostic utility pending prospective validation.
Pulmonary hypertension (PH) is a common complication of chronic obstructive pulmonary disease (COPD) and induces increased mortality among COPD patients. However, there are no blood biomarkers to identify PH in COPD. Here, we investigated whether circulating angiogenic factors and cytokines could serve as (a) biomarker (s) for COPD-PH patients. Using Angiogenesis and Cytokine proteome profile array assay, we measured the level of 36 cytokines and 55 angiogenesis-associated proteins in plasma from four COPD patients with PH (COPD-PH) and four COPD patients without PH (COPD), respectively, tissue inhibitor of metalloproteinase 1 (TIMP-1) and thrombospondin 1(TSP-1) were significantly different between the two groups. Enzyme-linked immunosorbent assay (ELISA) was applied to measured TIMP-1 and TSP-1 in a validation cohort (COPD-PH, n = 28; COPD, n = 18), and TIMP-1 was the only factor that was significantly different between COPD-PH and COPD patients (P < 0.01). Logistic regression analysis demonstrated that elevated TIMP-1 was an independent risk factor for COPD-PH [odds ratio (OR) = 1.258, 95% CI: 1.005–1.574, P < 0.05). Next, we explored the expression level and function of TIMP-1 in human pulmonary arterial smooth muscle cells (hPASMCs) exposed to cigarette smoking extract (CSE, a major etiological factor of COPD). In cultured hPASMCs, CSE treatment increased both TIMP-1 protein level and cell proliferation, and exogenous TIMP-1 (25 ng/mL) treatment inhibited CSE-induced hPASMCs proliferation. Overall, our results indicated that TIMP-1 elevation could serve as a circulating biomarker to diagnose PH among COPD patients, and TIMP-1 elevation in COPD-PH could be adaptive.
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He et al. (2022) conducted a case-control in Chronic obstructive pulmonary disease with pulmonary hypertension (n=54). Elevated TIMP-1 vs. COPD without pulmonary hypertension was evaluated on Diagnosis of pulmonary hypertension (COPD-PH) (OR 1.258, 95% CI 1.005-1.574, p=0.045). Elevated plasma TIMP-1 was identified as an independent risk factor for the diagnosis of pulmonary hypertension among patients with chronic obstructive pulmonary disease (OR 1.258).
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