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1.
Biochem Biophys Res Commun ; 553: 1-8, 2021 05 14.
Article in English | MEDLINE | ID: mdl-33752091

ABSTRACT

BACKGROUND AND AIMS: Hypercholesterolemia is characterized by the elevation of plasma total cholesterol level, especially low-density lipoprotein (LDL) cholesterol. This disease is usually caused by a mutation in genes such as LDL receptor, apolipoprotein B, or proprotein convertase subtilisin/kexin type 9. However, a considerable number of patients with hypercholesterolemia do not have any mutation in these candidate genes. In this study, we examined the difference in the metabolic level between patients with hypercholesterolemia and healthy subjects, and screened the potential biomarkers for this disease. METHODS: Analysis of plasma metabolomics in hypercholesterolemia patients and healthy controls was performed by gas chromatography-mass spectrometry and metabolic correlation networks were constructed using Gephi-0.9.2. RESULTS: First, metabolic profile analysis confirmed the distinct metabolic footprints between the patients and the healthy ones. The potential biomarkers screened by orthogonal partial least-squares discrimination analysis included l-lactic acid, cholesterol, phosphoric acid, d-glucose, urea, and d-allose (Variable importance in the projection > 1). Second, arginine and methionine metabolism were significantly perturbed in hypercholesterolemia patients. Finally, we identified that l-lactic acid, l-lysine, l-glutamine, and l-cysteine had high scores of centrality parameters in the metabolic correlation network. CONCLUSION: Plasma l-lactic acid could be used as a sensitive biomarker for hypercholesterolemia. In addition, arginine biosynthesis and cysteine and methionine metabolism were profoundly altered in patients with hypercholesterolemia.


Subject(s)
Biomarkers/blood , Biomarkers/metabolism , Hypercholesterolemia/blood , Hypercholesterolemia/metabolism , Metabolomics , Adolescent , Adult , Arginine/metabolism , Case-Control Studies , Cholesterol/metabolism , Cysteine/metabolism , Female , Gas Chromatography-Mass Spectrometry , Glucose/metabolism , Glutamine/metabolism , Humans , Lactic Acid/blood , Lactic Acid/metabolism , Lysine/metabolism , Male , Methionine/metabolism , Middle Aged , Phosphoric Acids/metabolism , Urea/metabolism , Young Adult
2.
Ann Vasc Surg ; 47: 62-68, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28739463

ABSTRACT

BACKGROUND: The long-term efficacy of mesoatrial shunt (MAS) for Budd-Chiari syndrome (BCS) is not well studied. The purpose of our study was to investigate the long-term outcome and efficacy of MAS for BCS. METHODS: We retrospectively evaluated 11 patients who underwent MAS for BCS from April 1986 to November 1995. Records of patients' clinical presentations, laboratorial investigation, Doppler duplex ultrasonography, radiologic image, and treatment outcomes were all retrieved and analyzed. RESULTS: Follow-up intervals ranged from 1 year and 2 months to 30 years and 2 months (mean, 17 years and 8 months). Portal pressure decreased significantly from 35.72 ± 3.52 cm H2O to 27.86 ± 5.83 cm H2O post-MAS (P = 0.001). The 5-year, 10-year, and 20-year patency were 72.7%, 54.5%, 36.4%, respectively; 63.3% of patients had survived for more than 10 years and 45.5% for more than 20 years. A male has been alive with patent shunt for 28 years and 1 month. CONCLUSIONS: The MAS with enforced rings is an effective therapeutic modality for BCS with cautious perioperative management.


Subject(s)
Budd-Chiari Syndrome/surgery , Heart Atria/surgery , Mesenteric Veins/surgery , Portasystemic Shunt, Surgical/methods , Adult , Angiography , Budd-Chiari Syndrome/diagnostic imaging , Decompression, Surgical , Female , Humans , Longitudinal Studies , Male , Mesenteric Veins/diagnostic imaging , Portasystemic Shunt, Surgical/instrumentation , Retrospective Studies , Vena Cava, Inferior/diagnostic imaging , Young Adult
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