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1.
BMC Cardiovasc Disord ; 24(1): 315, 2024 Jun 22.
Article in English | MEDLINE | ID: mdl-38909188

ABSTRACT

INTRODUCTION: Fibrosing mediastinitis (FM) is a rare disease characterized by excessive proliferation of fibrous tissue in the mediastinum and can cause bronchial stenosis, superior vena cava obstruction, pulmonary artery and vein stenosis, etc. CASE PRESENTATION: An aging patient with intermittent chest tightness and shortness of breath was diagnosed with FM associated pulmonary hypertension (FM-PH) by echocardiography and enhanced CT of the chest, and CT pulmonary artery (PA)/ pulmonary vein (PV) imaging revealed PA and PV stenosis. Selective angiography revealed complete occlusion of the right upper PV, and we performed endovascular intervention of the total occluded PV. After failure of the antegrade approach, the angiogram revealed well-developed collaterals of the occluded RSPV-V2b, so we chose to proceed via the retrograde approach. We successfully opened the occluded right upper PV and implanted a stent. CONCLUSIONS: This report may provide new management ideas for the interventional treatment of PV occlusion.


Subject(s)
Pulmonary Veins , Stents , Humans , Treatment Outcome , Pulmonary Veins/diagnostic imaging , Pulmonary Veins/physiopathology , Pulmonary Veins/surgery , Chronic Disease , Pulmonary Veno-Occlusive Disease/therapy , Pulmonary Veno-Occlusive Disease/diagnostic imaging , Pulmonary Veno-Occlusive Disease/physiopathology , Pulmonary Veno-Occlusive Disease/etiology , Stenosis, Pulmonary Vein/diagnostic imaging , Stenosis, Pulmonary Vein/therapy , Stenosis, Pulmonary Vein/physiopathology , Stenosis, Pulmonary Vein/etiology , Mediastinitis/diagnosis , Mediastinitis/therapy , Male , Phlebography , Angioplasty, Balloon/instrumentation , Aged , Hypertension, Pulmonary/physiopathology , Hypertension, Pulmonary/therapy , Hypertension, Pulmonary/etiology , Hypertension, Pulmonary/diagnostic imaging , Fibrosis , Collateral Circulation , Pulmonary Circulation , Female
2.
Clin Rheumatol ; 43(6): 1979-1987, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38598024

ABSTRACT

OBJECTIVE: The goal of the present study was to investigate the correlation between serum 25-hydroxyvitamin D [25(OH)D] levels and disease remission in Takayasu arteritis (TAK) patients. METHODS: This retrospective study included 59 patients in the study group and 80 patients in the validation cohort with TAK. After 6 months of therapy, patients were re-evaluated, and serum 25(OH)D levels were compared before and after treatment. Correlations between changes in 25(OH)D levels and changes in disease activity scores (NIH, ITAS2010, ITAS.A) were analyzed. Additionally, a predictive cut-off value for disease remission was determined. RESULTS: After 6 months of therapy, serum 25(OH)D levels in TAK patients significantly increased compared to baseline [(18.33 ± 7.25)µg/L vs (11.77 ± 4.14) µg/L] (P < 0.001). Positive correlations were observed between the increasing changes in the 25(OH)D level and the decreasing changes in the reduced NIH, ITAS2010, and ITAS.A scores (r = 0.455, P < 0.001; r = 0.495, P < 0.001; and r = 0.352 P = 0.006, respectively). A change of 8.45 µg/L in 25(OH)D level was identified as the predictive cut-off value for TAK remission (sensitivity 54.1%, specificity 90.9%, area under the curve = 0.741). Similarly for patients with normal baseline ESR, sensitivity is 68.0%, specificity is 92.3%, and area under the curve is 0.831, and for patients with normal baseline CRP, sensitivity is 58.3%, specificity is 90.0%, and area under the curve is 0.748. Validation in an additional 80 patients demonstrated a higher remission rate in those with a 25(OH)D level change > 8.45 µg/L. CONCLUSION: Serum 25(OH)D levels significantly increased after treatment in TAK patients, and an increase of ≥ 8.45 µg/L was predictive of disease remission, especially in individuals with normal baseline ESR and/or CRP levels. Key Points • Following treatment, there was a significant increase in serum 25(OH)D levels among TAK patients. • The elevated changes in 25(OH)D levels before and after treatment demonstrated a positive correlation with the reduction in disease activity scores. • In patients with TAK before and after treatment, an elevation in serum 25(OH)D levels exceeding 8.45 µg/L serves as an indicator for disease remission, particularly prominent in individuals with normal baseline ESR and/or CRP levels.


Subject(s)
Blood Sedimentation , C-Reactive Protein , Remission Induction , Takayasu Arteritis , Vitamin D , Humans , Female , Retrospective Studies , Male , Vitamin D/analogs & derivatives , Vitamin D/blood , Adult , Takayasu Arteritis/blood , Takayasu Arteritis/drug therapy , C-Reactive Protein/metabolism , C-Reactive Protein/analysis , Young Adult , Middle Aged , Severity of Illness Index , Adolescent , Biomarkers/blood
3.
Front Immunol ; 15: 1371706, 2024.
Article in English | MEDLINE | ID: mdl-38650935

ABSTRACT

Pulmonary hypertension (PH) pathogenesis is driven by inflammatory and metabolic derangements as well as glycolytic reprogramming. Induction of both interleukin 6 (IL6) and transglutaminase 2 (TG2) expression participates in human and experimental cardiovascular diseases. However, little is known about the role of TG2 in these pathologic processes. The current study aimed to investigate the molecular interactions between TG2 and IL6 in mediation of tissue remodeling in PH. A lung-specific IL6 over-expressing transgenic mouse strain showed elevated right ventricular (RV) systolic pressure as well as increased wet and dry tissue weights and tissue fibrosis in both lungs and RVs compared to age-matched wild-type littermates. In addition, IL6 over-expression induced the glycolytic and fibrogenic markers, hypoxia-inducible factor 1α, pyruvate kinase M2 (PKM2), and TG2. Consistent with these findings, IL6 induced the expression of both glycolytic and pro-fibrogenic markers in cultured lung fibroblasts. IL6 also induced TG2 activation and the accumulation of TG2 in the extracellular matrix. Pharmacologic inhibition of the glycolytic enzyme, PKM2 significantly attenuated IL6-induced TG2 activity and fibrogenesis. Thus, we conclude that IL6-induced TG2 activity and cardiopulmonary remodeling associated with tissue fibrosis are under regulatory control of the glycolytic enzyme, PKM2.


Subject(s)
Fibroblasts , GTP-Binding Proteins , Hypertension, Pulmonary , Interleukin-6 , Lung , Mice, Transgenic , Protein Glutamine gamma Glutamyltransferase 2 , Pyruvate Kinase , Transglutaminases , Animals , Humans , Mice , Disease Models, Animal , Fibroblasts/metabolism , Fibrosis , GTP-Binding Proteins/metabolism , GTP-Binding Proteins/genetics , Hypertension, Pulmonary/metabolism , Hypertension, Pulmonary/pathology , Hypertension, Pulmonary/etiology , Interleukin-6/metabolism , Lung/pathology , Lung/immunology , Lung/metabolism , Pulmonary Fibrosis/metabolism , Pulmonary Fibrosis/pathology , Pyruvate Kinase/metabolism , Pyruvate Kinase/genetics , Transglutaminases/metabolism , Transglutaminases/genetics
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