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1.
Am J Cardiol ; 108(3): 360-6, 2011 Aug 01.
Article in English | MEDLINE | ID: mdl-21757044

ABSTRACT

Preß-1 high-density lipoprotein (HDL) plays a key role in reverse cholesterol transport by promoting cholesterol efflux. Our aims were (1) to test previous associations between preß-1 HDL and coronary heart disease (CHD) and (2) to investigate whether preß-1 HDL levels also are associated with risk of myocardial infarction (MI). Plasma preß-1 HDL was measured by an ultrafiltration-isotope dilution technique in 1,255 subjects recruited from the University of California-San Francisco Lipid and Cardiovascular Clinics and collaborating cardiologists. Preß-1 HDL was significantly and positively associated with CHD and MI even after adjustment for established risk factors. Inclusion of preß-1 HDL in a multivariable model for CHD led to a modest improvement in reclassification of subjects (net reclassification index 0.15, p = 0.01; integrated discrimination improvement 0.003, p = 0.2). In contrast, incorporation of preß-1 HDL into a risk model of MI alone significantly improved reclassification of subjects (net reclassification index 0.21, p = 0.008; integrated discrimination improvement 0.01, p = 0.02), suggesting that preß-1 HDL has more discriminatory power for MI than for CHD in our study population. In conclusion, these results confirm previous associations between preß-1 HDL and CHD in a large well-characterized clinical cohort. Also, this is the first study in which preß-1 HDL was identified as a novel and independent predictor of MI above and beyond traditional CHD risk factors.


Subject(s)
Coronary Disease/blood , High-Density Lipoproteins, Pre-beta/blood , Myocardial Infarction/blood , Adult , Aged , Cohort Studies , Coronary Disease/diagnosis , Coronary Disease/epidemiology , Female , Humans , Likelihood Functions , Male , Middle Aged , Myocardial Infarction/diagnosis , Myocardial Infarction/epidemiology , Predictive Value of Tests , Risk Factors
2.
Interact Cardiovasc Thorac Surg ; 12(2): 141-5, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21109618

ABSTRACT

The purpose of this study is to analyze the immediate results of bidirectional cavopulmonary anastomosis (BCPA) and Fontan operations performed in adults, and to reveal the risk factors. During the years 1983-2010, 681 consecutive patients underwent BCPA or a Fontan operation. Fifty-three of 681 patients were more than 18 years of age. Twenty-nine adults underwent BCPA and 24 underwent a Fontan operation. Immediate results of surgical treatment were followed during the hospital period. The average number of exceeded 'operability' criteria by Choussat et al. [Choussat A, Fontan F, Besse P, Vallot F, Chauve A, Bricaud H. Selection criteria for Fontan procedure. In: Anderson RH, Shinebourne EA, editors. Pediatric Cardiology. Edinburgh: Churchhill Livingstone, 1977:559-566] was significantly higher in patients from the BCPA group compared to the Fontan group (1.3±0.8 vs. 0.9±0.7, P=0.034). Hospital mortality after BCPA in adults was 6.9% (2/29) and did not differ from children (7.1%, 19/268), P=0.634. Hospital mortality after Fontan operation in adults was 8.3% (2/24) and did not differ from children (11.9%, 43/360), P=0.419. The frequency of non-lethal hospital complications was higher in patients after a Fontan operation. Patients from the Fontan group more frequently developed arrhythmias and prolonged pleural effusions. Preoperative regurgitation at atrioventricular valves was an independent risk factor for hospital mortality and morbidity after a Fontan operation. BCPA and Fontan operations performed in adults are accompanied by good immediate results and considerably improves patients' condition.


Subject(s)
Heart Bypass, Right/methods , Heart Defects, Congenital/mortality , Heart Defects, Congenital/surgery , Hemodynamics/physiology , Adolescent , Adult , Analysis of Variance , Cohort Studies , Confidence Intervals , Female , Follow-Up Studies , Fontan Procedure/methods , Fontan Procedure/mortality , Heart Bypass, Right/mortality , Heart Defects, Congenital/diagnosis , Hospital Mortality/trends , Humans , Logistic Models , Male , Multivariate Analysis , Odds Ratio , Postoperative Complications/diagnosis , Postoperative Complications/mortality , Pulmonary Circulation/physiology , Retrospective Studies , Risk Assessment , Survival Analysis , Time Factors , Treatment Outcome , Young Adult
3.
Neuropeptides ; 31(1): 52-9, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9574838

ABSTRACT

It has been previously found that chloromethyl ketone derivatives of enkephalins bind irreversibly to the opioid receptors in vitro. Recently a novel affinity reagent, Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Gly chloromethyl ketone (Dynorphin(1-10)-Gly11 chloromethyl ketone, DynCMK) was synthesized, and its binding characteristics to frog (Rana esculenta) brain membranes were evaluated. In competition experiments, the product shows a relatively high affinity for the kappa-opioid binding sites labelled by [3H]ethylketocyclazocine (Ki is approximately equal to 200 nM), whereas its binding to the 1 ([3H]dihydromorphine) and to the delta sites ([3H]D-Ala2-Leu5]enkephalin) is weaker. Preincubation of the frog brain membranes with DynCMK at micromolar concentrations results in a washing-resistant and dose-dependent inhibition of the [3H]ethylketocyclazocine binding sites. Saturation binding analysis of the membranes preincubated with 50 microM DynCMK reveals a significant decrease in the number of specific binding sites for [3H]ethylketocyclazocine compared to the control values. The kappa-preferring binding properties of the compound suggest that it could serve as an affinity label for the kappa-type of opioid receptors.


Subject(s)
Amino Acid Chloromethyl Ketones/pharmacology , Brain Chemistry/physiology , Dynorphins/pharmacology , Peptide Fragments/pharmacology , Receptors, Opioid/analysis , Affinity Labels/pharmacology , Amino Acid Chloromethyl Ketones/chemical synthesis , Amino Acid Chloromethyl Ketones/metabolism , Analgesics, Opioid/pharmacology , Animals , Binding, Competitive/physiology , Dihydromorphine/pharmacology , Dynorphins/chemical synthesis , Dynorphins/metabolism , Enkephalin, Leucine-2-Alanine/pharmacology , Ethylketocyclazocine/pharmacology , Membrane Proteins/analysis , Peptide Fragments/chemical synthesis , Peptide Fragments/metabolism , Radioligand Assay , Rana esculenta , Receptors, Opioid/metabolism , Receptors, Opioid, kappa/agonists , Tritium
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