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1.
J Nephrol ; 32(1): 129-137, 2019 Feb.
Article in English | MEDLINE | ID: mdl-29946864

ABSTRACT

AIMS: Chronic kidney disease (CKD) is a common complication after liver transplantation (LT). The etiology of CKD is broad and may only be assessed accurately by renal histology. The current study aimed to analyze the safety of renal biopsy in daily clinical practice as well as its usefulness regarding management of CKD after LT. METHODS: We performed a retrospective analysis of clinical data and renal biopsies obtained from patients with severe renal impairment (overt proteinuria, progressive deterioration of renal function) after LT with respect to safety, etiology of renal disease, and therapeutic consequences. RESULTS: Renal biopsies were obtained from 14 patients at median (minimum-maximum) 3 (0.2-12) years after LT. No major complications associated with renal biopsy were observed. Histomorphological alterations were varied (nephrosclerosis, n = 5; IgA-glomerulonephritis, n = 4; tenofovir-associated nephropathy, membranoproliferative glomerulonephritis type 1, membranous glomerulonephritis, amyloid A amyloidosis, and calcineurin inhibitor nephropathy, n = 1, respectively). The diagnosis of specific renal diseases other than calcineurin-inhibitor nephrotoxicity facilitated specific treaments and avoided unnecessary modification of immunosuppression in the majority of patients. CONCLUSIONS: Renal biopsy in patients with CKD after LT seems safe and may offer specific therapeutic options. Furthermore, unnecessary changes of immunosuppression can be avoided in a considerable number of patients.


Subject(s)
Kidney/pathology , Liver Transplantation/adverse effects , Renal Insufficiency, Chronic/pathology , Adult , Aged , Disease Progression , Female , Humans , Immunosuppressive Agents/adverse effects , Kidney/physiopathology , Male , Middle Aged , Proteinuria/etiology , Proteinuria/pathology , Proteinuria/physiopathology , Renal Insufficiency, Chronic/etiology , Renal Insufficiency, Chronic/physiopathology , Renal Insufficiency, Chronic/therapy , Retrospective Studies , Risk Assessment , Risk Factors , Time Factors , Treatment Outcome
2.
Atherosclerosis ; 200(2): 403-9, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18262188

ABSTRACT

OBJECTIVE: An inverse association of adiponectin with coronary heart disease (CHD) has been reported, but the results are inconsistent. We used data from the CORA study to investigate into plasma concentrations of adiponectin and factors that may mediate the link to incident CHD. DESIGN: The CORA study is a population-based case-control study on 200 women with incident CHD and 255 age-matched controls. RESULTS: Plasma concentrations of adiponectin were significantly lower in women with CHD (p<0.0001), and in women with BMI >or=25 kg/m(2) (p<0.02), even more so with central obesity (WHR >or=0.85), prevalent diabetes or insulin resistance (HOMA-IR >or=3.8), or low HDL-cholesterol (<50mg/dl), and in smokers (each p<0.0001). Adiponectin also correlated with intake of fruit and vegetables, meat and sausage and alcohol as dietary markers of cardiovascular risk. Strikingly, the trend towards lower adiponectin concentrations with increasing BMI or waist circumference was less marked than the difference of adiponectin between CHD cases and controls. In a logistic regression model the odds ratio of adiponectin of 0.943 per 1 microg/ml (CI 0.919-0.968, p<0.0001) for risk of CHD was progressively reduced by elevated WHR, obesity-related risk factors, smoking, and dietary parameters. CONCLUSIONS: Plasma adiponectin indicates protection from CHD in women that is attenuated by combined effects of central obesity and dependent risk factors, parameters of nutrition and smoking. Thus, the impact of adiponectin goes beyond its relation to central adiposity, but may also reflect independent effects of lifestyle.


Subject(s)
Adiponectin/blood , Atherosclerosis/blood , Atherosclerosis/diagnosis , Coronary Artery Disease/blood , Coronary Artery Disease/diagnosis , Adiponectin/metabolism , Adult , Age Factors , Aged , Aged, 80 and over , Body Mass Index , Case-Control Studies , Female , Humans , Life Style , Middle Aged , Risk Factors , Smoking
3.
Diab Vasc Dis Res ; 4(2): 136-42, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17654448

ABSTRACT

In most developed and developing countries, the proportion of the population aged 60 years or more is growing faster than any other age group. Given that the vast majority of cardiovascular events occur in older individuals, new thinking is needed to reduce their risk. Epidemiological studies have shown an increasing prevalence of the metabolic syndrome with age, driven by nutrition inappropriate for a modern sedentary lifestyle. A low level of high-density lipoprotein (HDL)-cholesterol, a component of the atherogenic dyslipidaemia of the metabolic syndrome, has been shown to be an important determinant of coronary risk, which rises in prevalence with increasing age. Thus, raising HDLcholesterol, in addition to lowering the level of low-density lipoprotein (LDL)-cholesterol, seems a plausible approach to reduce cardiovascular risk in an ageing population. Clinical studies have shown that adding nicotinic acid, which raises HDL-cholesterol by 20-25%, to a statin enhances the reduction in progression of atherosclerosis. Results of the ongoing Atherothrombosis Intervention in Metabolic syndrome with low HDL/High triglyceride and Impact on Global Health Outcomes (AIM-HIGH) study are awaited with interest to see whether such theoretical benefit translates into clinical outcome.


Subject(s)
Aging/blood , Cardiovascular Diseases/etiology , Cholesterol, HDL/blood , Dyslipidemias/blood , Hypolipidemic Agents/therapeutic use , Age Factors , Aged , Cardiovascular Diseases/blood , Cardiovascular Diseases/prevention & control , Cholesterol, LDL/blood , Drug Therapy, Combination , Dyslipidemias/complications , Dyslipidemias/drug therapy , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Middle Aged , Niacin/therapeutic use , Risk Assessment , Risk Factors , Treatment Outcome , Triglycerides/blood
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