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"apellidos" => "Hernández-Gallego" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "affc" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Servicio de Nefrología, Hospital Infanta Cristina, Badajoz, Spain, " "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "affb" ] 1 => array:3 [ "entidad" => "Servicio de Nefrología, Hospital Infanta Cristina, Badajoz, " "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "affc" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Resistencia a la insulina en la enfermedad renal crónica: características clínicas asociadas y significado pronóstico" ] ] "textoCompleto" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">INTRODUCTION</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Insulin resistance (IR), which is characterized by a functional deficit in this hormone despite high plasma levels, leads to a series of changes in the composition of plasma lipids, coagulation, endothelial function and vascular resistance, as well as endocrine changes and obesity. In combination, this increases the risk of developing high blood pressure and accelerated atherosclerosis.<span class="elsevierStyleSup">1-4</span> The increase in cardiovascular risk associated with IR has been shown in the general population.<span class="elsevierStyleSup">1-4</span> </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The biochemical data of a high proportion of patients with chronic kidney disease (CKD) is compatible with IR,<span class="elsevierStyleSup">5-8</span> even in the earliest stages of renal insufficiency. Although this metabolic disorder, which is associated with uraemia, was first described in the 1980s by DeFronzo and Alvestrand,<span class="elsevierStyleSup">9,10</span> its physiopathological mechanisms are not yet fully understood.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">CKD patients have a very high risk of developing cardiovascular (CV) diseases<span class="elsevierStyleSup">11,12</span> and the link between these processes and traditional CV risk factors is specific.<span class="elsevierStyleSup">13</span> The role that IR plays in the development of CV disease and mortality in the CKD population has not been subject of many studies.<span class="elsevierStyleSup">7,14-16</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The objectives of this study were to determine the prevalence and clinical and biochemical characteristics associated with IR in a patient population with advanced CKD prior to dialysis, and to establish the prognostic value of IR in the progression of CKD, the development of new CV processes and all-cause mortality.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">MATERIAL AND METHODS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold"> </span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Patients</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In the study, 365 patients (average age 63±16 years, 169 females) with stage 4-5 chronic kidney disease, who were monitored by a specialist in advanced chronic kidney disease (ACKD) were included. The inclusion criteria were as follows: patients over 18 years of age with no previous diagnosis of diabetes mellitus and baseline (fasting) blood glucose levels below 126 mg/dl, in a stable clinical condition with no acute intercurrent disease at the time of the baseline study and receiving no treatment with corticoids or other drugs with a significant “anti-insulin” action.  </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The aetiology of renal insufficiency was: undetermined origin (154 patients), primary glomerulonephritis (76 patients), chronic interstitial nephritis (66 patients), polycystic disease (31 patients), ischaemic nephropathy (30 patients) and other etiologies (8 patients). </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Although none of the patients included in the study had diabetes mellitus, other comorbid diseases were common: 41 patients had a previous history of ischaemic cardiopathy, 55 of heart failure, 61 of cerebral or peripheral vascular disease, 23 of malignant disease and 40 of chronic obstructive pulmonary disease, and 19 patients had other significant comorbidities.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The drugs which were most frequently prescribed were anti-hypertensive agents (angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, betablockers), diuretics, statins, antiplatelet drugs and phosphate binders. </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">Clinical Data and Laboratory Analysis</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In addition to demographic data, systolic and diastolic blood pressure measurements, and body mass index were included. Comorbidity levels were quantified using the method developed by Davies et al.<span class="elsevierStyleSup">17</span> Because of their potential link to insulin resistance, variables included the regular consumption of drugs such as betablockers, diuretics and angiotensin-converting enzyme inhibitors (ACEI) and/or angiotensin receptor antagonists (ARA). </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Blood samples were taken from patients after a prolonged fasting period (at least 8 hours) in order to determine the following parameters: haemogram, glucose, urea, creatinine, uric acid, calcium, phosphate, total cholesterol, triglycerides, albumin (Advia Chemistry Multianalyzer, Siemens Healthcare Diagnostics) and venous bicarbonate (ABL 800 FLEX analyzer). The plasma concentration of highly sensitive C-reactive protein was determined by nephelometry (N High Sensitivity CRP, Behring, Marburg, Germany). The plasma concentrations of PTH were determined by IRMA (1-84 N-tact PTH IRMA Diasorin).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Glomerular filtration was estimated by means of the 4-variable MDRD formula. The protein catabolic rate (NPNA) was calculated by measuring urinary nitrogen excretion using the combined formulas of Cottini et al and Maroni et al, in accordance with the description given by Bergström et al.<span class="elsevierStyleSup">18</span> The NPNA was adjusted to the actual weight of the patient.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Plasma concentrations of insulin were determined by means of two-site, solid-phase chemiluminiscent immunometric assays (Immulite<span class="elsevierStyleSup">®</span> 2000 Immunoassay System Siemens Healthcare Diagnostics). The intra-assay and total coefficients of variation were 6.1 and 7.1% respectively.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">To establish the level of insulin resistance we used the Homeostasis Model Assessment Insulin Resistance (HOMA)<span class="elsevierStyleSup">19</span> parameter, the utility and reliability of which have been validated in patients with chronic kidney failure.<span class="elsevierStyleSup">20</span> This parameter is calculated by means of the following formula: fasting insulin (µU/ml) x fasting glucose (mmol/l)/22.5.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">Study Design and Statistical Analysis</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">This study is divided into two section, a first section consisting of a transversal analysis, in which the clinical and analytical characteristics associated with different levels of insulin resistance are described, and a second section, in which, by means of a prospective analysis, an attempt is made to establish the prognostic value of the HOMA parameter on three outcome events: <span class="elsevierStyleItalic">a)</span> CKD progression, defined as the initiation of dialysis or the doubling of baseline serum creatinine; <span class="elsevierStyleItalic">b)</span> the development of new severe acute cardiovascular processes (myocardial infarction, unstable angina, the need for coronary intervention, transistory or established cerebrovascular accidents or severe ischaemia of the lower limbs) and <span class="elsevierStyleItalic">c)</span> all-cause mortality.  </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">After an initial assessment, patients were monitored by means of regular visits every 1-3 months, while they continued to be seen by a specialist due to ACKD, or by the reporting of any change in the progression of the disease after the initiation of dialysis. Patients were ruled out for study purposes in cases of all-cause mortality, renal transplant, follow-up losses (16 patients) or completion of the study period (1 November 2008). Censoring date considered for patients who were lost was their last consultation.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Median follow-up until the initiation of dialysis was 542 days (interquartile ranges: 221–922 days) and median follow-up until death or censoring date was 1,103 days (interquartile ranges: 643–1,707 days).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The comparison of continuous variables between groups was performed using analysis of variance (ANOVA) or the Kruskal-Wallis test, depending on the distribution characteristics of the variables. The Scheffe test was used for <span class="elsevierStyleItalic">post hoc</span> comparisons. For the comparison of two independent continuous variables the Student’s t test for unpaired samples was used or the non-parametric Mann-Whitney test, depending on the distribution characteristics of the variables. The chi-square test was employed to compare discrete variables.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">To analyze the variables that showed the best links with the HOMA parameter (continuous variable), multivariate linear regression models were used, covariables being automatically selected by the (backward) conditional elimination process.  </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">To establish whether there was an independent link between the HOMA parameter and study outcomes, multivariate Cox proportional hazard models were used and the relative risks and 95% confidence intervals were determined. The HOMA parameter was analyzed both as a continuous and a discrete entity (terciles). </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The models were adjusted by introducing variables or risk factors with a potential influence on the final events which were the subject of the study (age, sex, comorbidity index, plasma albumin, C-reactive protein, residual renal function, proteinuria, etc.). The selection of the variables which best fitted the models was done automatically by the progressive conditional elimination process.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">To confirm risk proportionality, in all the survival studies we examined the graphs which were obtained by correlating the logarithm (-survival rate logarithm) with the survival time logarithm, as well as the graphs correlating the partial residues of each covariable against survival time. </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The percentage of missing data was below 1% for all the variables. The quantitative variables which were lost were made up by adding the arithmetic mean value for the rest of the present data.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The data for this study are presented as the mean plus standard deviation (± SD) or as the median and interquartile ranges or minimum-maximum value. A p value of <0.05 was regarded as statistically significant. The SPSS software version 15.0 (SPSS, Chicago, USA) was used for the statistical analysis and graphs.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">RESULTS</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold"> </span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Clinical Characteristics Associated with Insulin Resistance</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The average insulin and HOMA parameter values were: 17.31 ± 7.54 mU/ml and 4.28 ± 2.07 mU/ml x mmol/l respectively. </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The clinical and biochemical characteristics of the patients grouped into terciles according to the distribution frequency of the HOMA parameter are shown in table 1. Significant differences were not observed for age, sex, comorbidity index, percentage of patients with ischaemic cardiopathy and proteinuria. In patients in the upper tercile, glomerular filtration was significantly lower than in patients in the lower tercile. Patients in the upper HOMA terciles had a higher body mass index than patients in the lower tercile. Although differences were not observed in total plasma cholesterol concentrations, upper HOMA tercile patients showed significantly higher triglyceride levels than those in the other terciles. Serum phosphate levels were also higher in upper tercile patients than in the remaining terciles.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Other significant differences between terciles were detected for plasma albumin, bicarbonate and PTH (table 1).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">C-reactive protein levels were similar and there were no significant differences in the drugs prescribed in the three subgroups (table 1).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In the multiple linear regression models, the variables included in the best predictive equation for HOMA values were: body mass index, triglycerides, plasma albumin and serum phosphate levels (table 2).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">Insulin Resistance and CKD Progression</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">During the follow-up period 234 patients (64%) met the criteria for CKD progression (6 patients doubled their initial serum creatinine levels and 228 started dialysis). Using Kaplan-Meier survival analysis (Figure 1), it was noted that only patients in the lower HOMA tercile showed more prolonged survival without meeting CKD progression criteria (lower tercile compared to the rest of the patients: log rank=4.19; p=0.04).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In the Cox regression analysis, adjusted for variables which are potentially related to the progression of CKD (age, sex, body mass index, systolic and diastolic blood pressure, baseline glomerular filtration rate, proteinuria, haemoglobin, albumin, phosphate, bicarbonate, diabetes and anti-angiotensin treatment, calcium antagonists and diuretics), a HOMA value in the lower tercile continued to correlate significantly with a slower progression of CKD (table 3 and figure 2).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">Insulin Resistance and the Development of New Cardiovascular Disease Episodes or Mortality</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">During the follow-up period 51 patients presented a new cardiovascular episode and 104 died as a result of any cause. Using Kaplan-Meier survival curves, we failed to detect a significant correlation between HOMA terciles and the development of new CV episodes (log rank=0.117; NS) or with all-cause mortality (log rank=2.64; p=0.267).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In Cox regression models adjusted for age, sex, body mass index, comorbidity index, plasma albumin, C-reactive protein, baseline glomerular filtration rate, proteinuria, serum phosphate and antihypertensive medication, HOMA measured both as a continuous entity and in terciles showed no link either with the development of new CV processes (hazard ratio for the continuous variable=1.106; 95% CI, 0.901–1.358; p=0.337) or with all-cause mortality (HR continuous variable=1.091; 95% CI, 0.991–1.200; p=0.076).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The stratification of the models, based on a body mass index higher or lower than 30 kg/m<span class="elsevierStyleSup">2</span>, failed to substantially modify the results, although the correlation between HOMA and mortality occurred at the limit of statistical significance (HR HOMA terciles=1.28; p=0.060).</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><span class="elsevierStyleBold">DISCUSSION</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The results of this study show that the degree of severity of insulin resistance in ACKD is linked to obesity and plasma triglyceride, albumin and phosphate levels. Other parameters which show univariate correlation with HOMA values include glomerular filtration rate, serum bicarbonate and PTH. However, neither blood pressure values nor C-reactive protein levels or proteinuria magnitude correlate significantly with HOMA values.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Although there are no standard values for normalized HOMA parameter measurement (in theory a young healthy subject should have a value equivalent to one<span class="elsevierStyleSup">19</span>), the figures presented by the patients included in this study were very high (two thirds of the patients showed a value of >3), which confirms the high prevalence of this metabolic disorder in non-diabetic CKD.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Obesity is very prevalent in CKD.<span class="elsevierStyleSup">21</span> IR and obesity-linked hyperinsulinaemia have been implicated in the development of kidney disease and accelerated atherosclerosis.<span class="elsevierStyleSup">22,23</span> Obesity was very prevalent in the patients included in this study and was a significant factor in determining the degree of severity of IR, suggesting a pathogenic link in the development of this metabolic disorder, irrespective of any association which can be attributed to uraemia.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Hypertriglyceridaemia is pathogenically linked to IR.<span class="elsevierStyleSup">3,4</span> This lipid metabolism disorder is also very common in CKD.<span class="elsevierStyleSup">24</span> The results of this study show a significant link between HOMA values and plasma triglyceride levels, which suggests that IR has an important role in the development of this dislipidaemia in CKD.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The positive correlation between HOMA values and plasma albumin concentrations is a prominent finding in this study. Plasma albumin concentration reflects the presence and severity of different processes which have a negative impact on outcomes for CKD patients (e.g. poor nutrition, inflammation, hypervolaemia, etc.) and so this parameter is regarded as a “clinical index of disease”,<span class="elsevierStyleSup">25</span> determining mortality in most studies involving CKD patients.  </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In haemodialysis patients HOMA correlates positively with both the rate of synthesis and breakdown of muscle protein, although there is a tendency towards a negative correlation with net muscle protein balance.<span class="elsevierStyleSup">26</span> While these findings suggest that IR has a negative effect on nutritional status, other studies in pre-dialysis CKD patients show that the amount of protein intake determines hyperinsulinaemia levels and sensitivity to insulin, IR improving in patients on low protein and phosphate diets.<span class="elsevierStyleSup">27-29</span></p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">A possible explanation for the positive correlation between HOMA and plasma albumin might be differences in protein intake and nutritional status between patients. Although in this study patients in the lower HOMA tercile showed a lower protein catabolic rate (NPNA) than upper tercile patients, the differences were not significant and therefore this hypothesis cannot be accepted.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">The plasma phosphate levels also show a positive correlation with HOMA values. In favour of the previous hypothesis, a diet which is inappropriate to the level of kidney failure might help to explain this finding. A reduction of phosphate in the diet has been shown to improve the degree of IR in CKD patients.<span class="elsevierStyleSup">28</span> We should also point out the potential link between insulin and the excretion of phosphate in urine. Insulin has an anti-phosphaturic effect,<span class="elsevierStyleSup">30,31</span> even antagonizing the phosphaturic action of PTH.<span class="elsevierStyleSup">32</span> In the present study estimates of phosphate were not made and, consequently, this hypothetical link between IR and phosphate cannot be confirmed.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Hyperinsulinaemia and IR predispose to the development or worsening of high blood pressure, and the development and progression of CKD, via mechanisms such as an increase in renal absorption of sodium, increased sympathetic activity, changes in endothelial and podocyte function, dislipidaemia, hyperglycaemia and increased renin-angiotensin activity.<span class="elsevierStyleSup">33</span> In some studies a link has been observed between the HOMA parameter and the rate of CKD progression in patients with glomerulonephritis,<span class="elsevierStyleSup">34</span> and between plasma insulin levels and the rate of progression of age-related renal deterioration.<span class="elsevierStyleSup">35</span>  </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">CKD progression, according to the criteria established in the present study, was slower in patients with a lower degree of IR (lower tercile). Although this finding is statistically significant, even after adjustment for other factors which determine the progression of CKD, and consistent with the potentially negative effects of hyperinsulinaemia, the clinical relevance of this finding does not appear to be very important, if we compare it with the effect of other factors (proteinuria, age, phosphate, etc.) on the progression of CKD.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Although IR is regarded as a cardiovascular and mortality risk factor in the general population,<span class="elsevierStyleSup">1-4</span> the impact of this metabolic disorder in the CKD population is the subject of controversy.<span class="elsevierStyleSup">7,14-16</span> In CKD the link between IR and mortality has only been observed in Japanese patients,<span class="elsevierStyleSup">14,16</span> while in other ethnic groups it has not been possible to demonstrate this relationship.<span class="elsevierStyleSup">7,15</span> </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">Neither do the results of this study support a link between the magnitude of the HOMA parameter and mortality or the development of new CV events in advanced CKD patients prior to dialysis, findings which once again differ from those observed in the general population.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">This study has limitations. The measurement of IR severity is based on a single HOMA parameter sample. The transversal design of the study to identify the determinants of the HOMA parameter limits its ability to adequately explain correlations. The absence of a link between HOMA levels and the development of new CV processes does not rule out a potential connection between IR and the severity and extent of vascular atherosclerotic damage which can be measured by more specific and sensitive procedures. The CKD progression criteria used in this study are not as reliable as the measurement and estimation of changes in glomerular filtration rate during the follow-up period.  </p><p class="elsevierStylePara"> </p><p class="elsevierStylePara">In conclusion, insulin resistance, estimated by the HOMA parameter, is prevalent in ACKD, although it does not seem to have a negative influence on the vital prognosis for these patients.</p><p class="elsevierStylePara"> </p><p class="elsevierStylePara"><a href="10491_108_11404_en_10491_18107_8318_es_10491_437_8318_es_tabla1.resistenciainsulina_en.doc" class="elsevierStyleCrossRefs">10491_108_11404_en_10491_18107_8318_es_10491_437_8318_es_tabla1.resistenciainsulina_en.doc</a></p><p class="elsevierStylePara">Table 1. Clinical and biochemical characteristics of patients grouped into HOMA parameter terciles</p><p class="elsevierStylePara"><a href="10491_108_11405_en_10491_18107_8319_es_10491_437_8319_es_tabla2.resistenciainsulina_en.doc" class="elsevierStyleCrossRefs">10491_108_11405_en_10491_18107_8319_es_10491_437_8319_es_tabla2.resistenciainsulina_en.doc</a></p><p class="elsevierStylePara">Table 2. Variables associated with the HOMA parameter according to multiple linear regression models</p><p class="elsevierStylePara"><a href="10491_108_11406_en_10491_18107_8320_es_10491_437_8320_es_tabla3.resistenciainsulina_en.doc" class="elsevierStyleCrossRefs">10491_108_11406_en_10491_18107_8320_es_10491_437_8320_es_tabla3.resistenciainsulina_en.doc</a></p><p class="elsevierStylePara">Table 3. Parameters included in the best predictive equation for CKD progression estimated by Cox regression models</p><p class="elsevierStylePara"><a href="10491_108_11407_en_10491_figuras_1__en.doc" class="elsevierStyleCrossRefs">10491_108_11407_en_10491_figuras_1__en.doc</a></p><p class="elsevierStylePara">Figure 1. Kaplan-Meier survival curves without CKD progression criteria according to HOMA terciles</p><p class="elsevierStylePara"><a href="10491_108_11408_en_10491_figuras_2__en.doc" class="elsevierStyleCrossRefs">10491_108_11408_en_10491_figuras_2__en.doc</a></p><p class="elsevierStylePara">Figure 2. Survival curves in patients with HOMA in the lower tercile (discontinuous line) and the rest of study patients (continuous line). The model is estimation after adjustment for age, sex, body mass index, albumin, proteinuria and phosphate</p>" "pdfFichero" => "P1-E506-S2860-A10491-EN.pdf" "tienePdf" => true "PalabrasClave" => array:2 [ "es" => array:5 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec441547" "palabras" => array:1 [ 0 => "Enfermedad renal crónica" ] ] 1 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec441549" "palabras" => array:1 [ 0 => "Mortalidad" ] ] 2 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec441551" "palabras" => array:1 [ 0 => "Riesgo cardiovascular" ] ] 3 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec441553" "palabras" => array:1 [ 0 => "Resistencia insulina" ] ] 4 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec441555" "palabras" => array:1 [ 0 => "Progresión insuficiencia renal" ] ] ] "en" => array:5 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec441548" "palabras" => array:1 [ 0 => "Chronic kidney disease" ] ] 1 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec441550" "palabras" => array:1 [ 0 => "Mortality" ] ] 2 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec441552" "palabras" => array:1 [ 0 => "Cardiovascular risk" ] ] 3 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec441554" "palabras" => array:1 [ 0 => "Insulin resistance" ] ] 4 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec441556" "palabras" => array:1 [ 0 => "Progression of renal insufficiency" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:1 [ "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold">Introduction</span><span class="elsevierStyleBold">: </span>Insulin resistance (IR) is a prevalent disorder in patients with chronic kidney disease (CKD). Little research has been done on how it is linked to cardiovascular (CV) morbidity and mortality in CKD. <span class="elsevierStyleBold">Objectives</span><span class="elsevierStyleBold">:</span> The aims of this study were to determine the links between IR and the progression of CKD, the development of new CV events and all-cause mortality in CKD patients prior to dialysis. <span class="elsevierStyleBold">Material and Methods</span><span class="elsevierStyleBold">: </span>Prospective, observational, cohort study including 365 non-diabetic patients (63±16 years, 169 female patients) with a glomerular filtration rate of <30 ml/min. The degree of IR was estimated by means of the Homeostasis Model Assessment (HOMA) parameter. The following event outcomes were analyzed: progression of CKD (initiation of dialysis or doubling of initial serum creatinine levels), development of new CV processes and all-cause mortality. <span class="elsevierStyleBold">Results</span><span class="elsevierStyleBold">: </span>Patients with HOMA values within the lower tercile (<3.13) showed slower CKD progression, based on a Cox regression model adjusted for age, sex, baseline glomerular filtration rate, body mass index and proteinuria (hazard ratio=0.72; p=0.03). During the total follow-up period 51 patients experienced new CV events and 103 died. The HOMA values did not correlate with the development of new CV events or mortality in either unadjusted models or models adjusted for age, sex, comorbidity index, serum albumin or C-reactive protein. <span class="elsevierStyleBold">Conclusions</span><span class="elsevierStyleBold">: </span>CKD progression was slower in patients with lower HOMA values, although this parameter failed to predict the development of new cardiovascular events or mortality.</p>" ] "es" => array:1 [ "resumen" => "<p class="elsevierStylePara"><span class="elsevierStyleBold"> </span></p> <p class="elsevierStylePara"><span class="elsevierStyleBold">Introducción: </span>La resistencia a la insulina (RI) es una alteración prevalente en los pacientes con enfermedad renal crónica (ERC). Su relación con la morbilidad cardiovascular (CV) y la mortalidad en la ERC ha sido poco estudiada. <span class="elsevierStyleBold">Objetivos:</span> Los objetivos de este estudio fueron determinar la relación de la RI con la progresión de la ERC, el desarrollo de nuevos eventos CV y la mortalidad por cualquier causa en pacientes con ERC prediálisis. <span class="elsevierStyleBold">Material y métodos: </span>Estudio de cohorte prospectivo observacional en el que se incluyeron 365 pacientes no diabéticos (63 ± 16 años, 169 mujeres) con un filtrado glomerular <30 ml/min. El grado de RI fue estimado mediante el parámetro «Homeostasis Model Assessment» (HOMA). Los sucesos evolutivos analizados fueron: progresión de ERC (entrada en diálisis o duplicar creatinina sérica inicial), desarrollo de nuevos procesos CV, o la mortalidad por cualquier causa. <span class="elsevierStyleBold">Resultados: </span>Los pacientes con valores HOMA en el tercil inferior (<3,13) mostraron una progresión más lenta de la ERC en un modelo de regresión de Cox ajustado a edad, sexo, filtrado glomerular basal, índice de masa corporal y proteinuria, (razón de riesgo = 0,72; p = 0,03). Durante el período total de seguimiento 51 pacientes desarrollaron nuevos eventos CV y 103 fallecieron. Los valores HOMA no se relacionaron con el desarrollo de nuevos eventos CV ni con la mortalidad en modelos no ajustados o ajustados a edad, sexo, índice de comorbilidad, albúmina sérica y proteína C reactiva. <span class="elsevierStyleBold">Conclusiones: </span>En conclusión, la progresión de la ERC fue más lenta en pacientes con los valores HOMA más bajos, aunque este parámetro no fue capaz de predecir el desarrollo de nuevos eventos cardiovasculares o la mortalidad.</p> <p class="elsevierStylePara"> </p> <p class="elsevierStylePara"><span class="elsevierStyleBold"> </span></p>" ] ] "multimedia" => array:5 [ 0 => array:8 [ "identificador" => "mmc1" "etiqueta" => "Tab. 1" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "Ecomponente" => array:2 [ "fichero" => "10491_108_11404_en_10491_18107_8318_es_10491_437_8318_es_tabla1.resistenciainsulina_en.doc" "ficheroTamanyo" => 49664 ] "descripcion" => array:1 [ "en" => "Clinical and biochemical characteristics of patients grouped into HOMA parameter terciles" ] ] 1 => array:8 [ "identificador" => "mmc2" "etiqueta" => "Tab. 2" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "Ecomponente" => array:2 [ "fichero" => "10491_108_11405_en_10491_18107_8319_es_10491_437_8319_es_tabla2.resistenciainsulina_en.doc" "ficheroTamanyo" => 33792 ] "descripcion" => array:1 [ "en" => "Variables associated with the HOMA parameter according to multiple linear regression models" ] ] 2 => array:8 [ "identificador" => "mmc3" "etiqueta" => "Tab. 3" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "Ecomponente" => array:2 [ "fichero" => "10491_108_11406_en_10491_18107_8320_es_10491_437_8320_es_tabla3.resistenciainsulina_en.doc" "ficheroTamanyo" => 42496 ] "descripcion" => array:1 [ "en" => "Parameters included in the best predictive equation for CKD progression estimated by Cox regression models" ] ] 3 => array:8 [ "identificador" => "mmc4" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "Ecomponente" => array:2 [ "fichero" => "10491_108_11407_en_10491_figuras_1__en.doc" "ficheroTamanyo" => 82432 ] "descripcion" => array:1 [ "en" => "Kaplan-Meier survival curves without CKD progression criteria according to HOMA terciles" ] ] 4 => array:8 [ "identificador" => "mmc5" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "Ecomponente" => array:2 [ "fichero" => "10491_108_11408_en_10491_figuras_2__en.doc" "ficheroTamanyo" => 64512 ] "descripcion" => array:1 [ "en" => "Survival curves in patients with HOMA in the lower tercile (discontinuous line) and the rest of study patients (continuous line). The model is estimation after adjustment for age, sex, body mass index, albumin, proteinuria and phosphate" ] ] ] "bibliografia" => array:2 [ "titulo" => "Bibliography" "seccion" => array:1 [ 0 => array:1 [ "bibliografiaReferencia" => array:35 [ 0 => array:3 [ "identificador" => "bib1" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Steinberg HO, Chaker H, Leaming R, Johnson A, Brechtel G, Baron AD. Obesity/insulin resistance is associated with endothelial dysfunction. Implications for the syndrome of insulin resistance. J Clin Invest 1996;97:2601-10. <a href="http://www.ncbi.nlm.nih.gov/pubmed/8647954" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 1 => array:3 [ "identificador" => "bib2" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Reaven GM, Lithell H, Landsberg L. Hypertension and associated metabolic abnormalities¿the role of insulin resistance and the sympathoadrenal system. N Engl J Med 1996;334:374-81. <a href="http://www.ncbi.nlm.nih.gov/pubmed/8538710" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 2 => array:3 [ "identificador" => "bib3" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Ginsberg HN. Insulin resistance and cardiovascular disease. J Clin Invest 2000;106:453-8. <a href="http://www.ncbi.nlm.nih.gov/pubmed/10953019" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 3 => array:3 [ "identificador" => "bib4" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "McFarlane SI, Banerji M, Sowers JR. Insulin resistance and cardiovascular disease. J Clin Endocrinol Metab 2001;86:713-8. <a href="http://www.ncbi.nlm.nih.gov/pubmed/11158035" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 4 => array:3 [ "identificador" => "bib5" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Eidemak I, Feldt-Rasmussen B, Kanstrup IL, Nielsen SL, Schmitz O, Strandgaard S. Insulin resistance and hyperinsulinemia in mild to moderate progressive chronic renal failure and its association with aerobic work capacity. Diabetologia 1995;38:565-72. <a href="http://www.ncbi.nlm.nih.gov/pubmed/7489839" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 5 => array:3 [ "identificador" => "bib6" "etiqueta" => "6" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Fliser D, Pacini G, Engelleiter R, Kautzky-Willer A, Prager R, Franek E, et al.\u{A0}Insulin resistance and hyperinsulinemia are already present in patients with incipient renal disease. Kidney Int 1998;53:1343-7. <a href="http://www.ncbi.nlm.nih.gov/pubmed/9573550" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 6 => array:3 [ "identificador" => "bib7" "etiqueta" => "7" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Becker B, Kronenberg F, Kielstein JT, Haller H, Morath C, Ritz E, et al.,\u{A0} MMKD Study Group. Renal insulin resistance syndrome, adiponectin and cardiovascular events in patients with kidney disease: the mild and moderate kidney disease study. J Am Soc Nephrol 2005;16:1091-8. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15743998" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 7 => array:3 [ "identificador" => "bib8" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Lorenzo C, Nath SD, Hanley AJ, Abboud HE, Haffner SM. Relation of low glomerular filtration rate to metabolic disorders in individuals without diabetes and with normoalbuminuria. Clin J Am Soc Nephrol 2008;3:783-9. <a href="http://www.ncbi.nlm.nih.gov/pubmed/18322051" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 8 => array:3 [ "identificador" => "bib9" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "DeFronzo RA, Alvestrand A, Smith D, Hendler R, Hendler E, Wahren J. Insulin resistance in uremia. J Clin Invest 1981;67:563-8. <a href="http://www.ncbi.nlm.nih.gov/pubmed/7007440" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 9 => array:3 [ "identificador" => "bib10" "etiqueta" => "10" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Alvestrand A, Mujagic M, Wajngot A, Efendic S. Glucose intolerance in uremic patients. The relative contributions of impaired beta-cell function and insulin resistance. Clin Nephrol 1989;31:175-83. <a href="http://www.ncbi.nlm.nih.gov/pubmed/2565775" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 10 => array:3 [ "identificador" => "bib11" "etiqueta" => "11" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Foley RN, Parfrey PS, Sarnak MJ. Epidemiology of cardiovascular disease in chronic renal disease. J Am Soc Nephrol 1998;9(Supl 12):S16-S23. <a href="http://www.ncbi.nlm.nih.gov/pubmed/11443763" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 11 => array:3 [ "identificador" => "bib12" "etiqueta" => "12" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Schiffri EL, Lipman ML, Mann JF. Chronic kidney disease: effects on the cardiovascular system. Circulation 2007;116:85-97. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17606856" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 12 => array:3 [ "identificador" => "bib13" "etiqueta" => "13" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Kalantar-Zadeh K, Block G, Humphreys MH, Kopple J. Reverse epidemiology of cardiovascular risk factors in maintenance dialysis patients. Kidney Int 2003;63:793-808. <a href="http://www.ncbi.nlm.nih.gov/pubmed/12631061" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 13 => array:3 [ "identificador" => "bib14" "etiqueta" => "14" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Shinohara K, Shoji T, Emoto M, Tahara H, Koyama H, Ishimura E, et al.\u{A0}Insulin resistance as an independent predictor of cardiovascular mortality in patients with end-stage renal disease. J Am Soc Nephrol 2002;13:1894-900. <a href="http://www.ncbi.nlm.nih.gov/pubmed/12089386" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 14 => array:3 [ "identificador" => "bib15" "etiqueta" => "15" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Menon V, Li L, Wang X, Greene T, Balakrishnan V, Madero M, et al.\u{A0}Adiponectin and mortality in patients with chronic kidney disease. J Am Soc Nephrol 2006;17:2599-606. <a href="http://www.ncbi.nlm.nih.gov/pubmed/16885405" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 15 => array:3 [ "identificador" => "bib16" "etiqueta" => "16" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Takenaka T, Kanno Y, Ohno Y, Suzuki H. Key role of insulin resistance in vascular injury among\u{A0} hemodialysis patients. Metabolism 2007;56:153-9. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17224326" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 16 => array:3 [ "identificador" => "bib17" "etiqueta" => "17" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Davies SJ, Phillips L, Naish PF, Russell GI. Quantifying comorbidity in peritoneal dialysis patients and its relationship to other predictors of survival. Nephrol Dial Transplant 2002;17:1085-92. <a href="http://www.ncbi.nlm.nih.gov/pubmed/12032201" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 17 => array:3 [ "identificador" => "bib18" "etiqueta" => "18" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Bergström J, Fürst P, Alvestrand A, Lindholm B. Protein and energy intake, nitrogen balance and nitrogen losses in patients treated with continuous ambulatory peritoneal dialysis. Kidney Int 1993;44:1048-57. <a href="http://www.ncbi.nlm.nih.gov/pubmed/8264134" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 18 => array:3 [ "identificador" => "bib19" "etiqueta" => "19" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment. Diabetologia 1985;28:412-9. <a href="http://www.ncbi.nlm.nih.gov/pubmed/3899825" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 19 => array:3 [ "identificador" => "bib20" "etiqueta" => "20" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Kanauchi M, Akai Y, Hashimoto T. Validation of simple indices to assess insulin sensitivity and pancreatic beta-cell function in patients with renal dysfunction. Nephron 2002;92:713-5. <a href="http://www.ncbi.nlm.nih.gov/pubmed/12372963" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 20 => array:3 [ "identificador" => "bib21" "etiqueta" => "21" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Abrass CK. Overview. Obesity: what does it have to do with kidney disease? J Am Soc Nephrol 2004;15:2768-72. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15504929" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 21 => array:3 [ "identificador" => "bib22" "etiqueta" => "22" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Bagby SP. Obesity-initiated metabolic syndrome and the kidney: A recipe for chronic kidney disease? J Am Soc Nephrol 2004;15:2775-91. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15504931" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 22 => array:3 [ "identificador" => "bib23" "etiqueta" => "23" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Schelling JR, Sedor JR. The metabolic syndrome as a risk factor for chronic kidney disease: More than a fat chance? J Am Soc Nephrol 2004;15:2773-4. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15504930" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 23 => array:3 [ "identificador" => "bib24" "etiqueta" => "24" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Kwan BCH, Kronenberg F, Beddhu S, Cheung AK. Lipoprotein metabolism and lipid management in chronic kidney disease. J Am Soc Nephrol 2007;18:1246-61. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17360943" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 24 => array:3 [ "identificador" => "bib25" "etiqueta" => "25" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Friedman AN, Fadem SZ. Reassessment of albumin as a nutritional marker in kidney disease. J Am Soc Nephrol 2010;21:223-30. <a href="http://www.ncbi.nlm.nih.gov/pubmed/20075063" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 25 => array:3 [ "identificador" => "bib26" "etiqueta" => "26" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Siew ED, Pupim LB, Majchrzak KM, Shintani A, Flakoll PJ, Ikizler TA. Insulin resistance is associated with skeletal muscle protein breakdown in non-diabetic chronic hemodialysis patients. Kidney Int 2007;71:146-52. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17063174" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 26 => array:3 [ "identificador" => "bib27" "etiqueta" => "27" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Gin H, Aparicio M, Potaux L, Merville P, Combe C, De Precigout V, et al.\u{A0}Low-protein, low-phosphorus diet and tissue insulin sensitivity in insulin-dependent diabetic patients with chronic renal failure. Nephron 1991;57:411-5. <a href="http://www.ncbi.nlm.nih.gov/pubmed/2046822" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 27 => array:3 [ "identificador" => "bib28" "etiqueta" => "28" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Gin H, Combe C, Rigalleau V, Delafaye C, Aparicio M, Aubertin J. Effects of a low-protein, low phosphorus diet on metabolic insulin clearance in patients with chronic renal failure. Am J Clin Nutr 1994;59:663-6. <a href="http://www.ncbi.nlm.nih.gov/pubmed/8116546" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 28 => array:3 [ "identificador" => "bib29" "etiqueta" => "29" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Rigalleau V, Blanchetier V, Combe C, Guillot C, Deleris G, Aubertin J, et al.\u{A0}A low-protein diet improves insulin sensitivity of endogenous glucose\u{A0} production in predialytic uremic patients. Am J Clin Nutr 1997;65:1512-6. <a href="http://www.ncbi.nlm.nih.gov/pubmed/9129485" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 29 => array:3 [ "identificador" => "bib30" "etiqueta" => "30" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "DeFronzo RA, Cooke CR, Andres R, Faloona GR, Davis PJ. The effect of insulin on renal handling of sodium, potassium, calcium, and phosphate in man. J Clin Invest 1975;55:845-55. <a href="http://www.ncbi.nlm.nih.gov/pubmed/1120786" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 30 => array:3 [ "identificador" => "bib31" "etiqueta" => "31" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Allón M, Rodríguez M, Llach F. Insulin in the acute renal adaptation to dietary phosphate restriction in the rat. Kidney Int 1990;37:14-20. <a href="http://www.ncbi.nlm.nih.gov/pubmed/1967663" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 31 => array:3 [ "identificador" => "bib32" "etiqueta" => "32" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Gunputalli J, Rogers A, Bourke E. Effect of insulin on renal phosphorus handling in the rat: Interaction with PTH and nicotinamide. Am J Physiol 1985; 249:F610-F618. <a href="http://www.ncbi.nlm.nih.gov/pubmed/2996369" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 32 => array:3 [ "identificador" => "bib33" "etiqueta" => "33" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "El-Atat FA, Stas SN, McFarlane SI, Sowers JR. The relationship between hyperinsulinemia, hypertension and progressive renal disease. J Am Soc Nephrol 2004;15:2816-27. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15504934" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 33 => array:3 [ "identificador" => "bib34" "etiqueta" => "34" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Kaartinen K, Syrjanen J, Porsti I, Harmoinen A, Pasternack A, Huhtala H, et al.\u{A0}Insulin resistance and the progression of IgA glomerulonephritis. Nephrol Dial Transplant 2007;22:778-83. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17166857" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 34 => array:3 [ "identificador" => "bib35" "etiqueta" => "35" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Oterdoom LH, De Vries AP, Gansevoort RT, De Jong PE, Gans RO, Bakker SJ. Fasting insulin modifies the relation between age and renal function. Nephrol Dial Transplant 2007;22:1587-92. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17314207" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/20132514/0000003000000006/v0_201502091649/X2013251410050927/v0_201502091649/en/main.assets" "Apartado" => array:4 [ "identificador" => "35441" "tipo" => "SECCION" "en" => array:2 [ "titulo" => "Originals" "idiomaDefecto" => true ] "idiomaDefecto" => "en" ] "PDF" => "https://static.elsevier.es/multimedia/20132514/0000003000000006/v0_201502091649/X2013251410050927/v0_201502091649/en/P1-E506-S2860-A10491-EN.pdf?idApp=UINPBA000064&text.app=https://revistanefrologia.com/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/X2013251410050927?idApp=UINPBA000064" ]
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2018 June | 35 | 17 | 52 |
2018 May | 45 | 16 | 61 |
2018 April | 50 | 6 | 56 |
2018 March | 45 | 10 | 55 |
2018 February | 43 | 16 | 59 |
2018 January | 32 | 6 | 38 |
2017 December | 47 | 13 | 60 |
2017 November | 55 | 11 | 66 |
2017 October | 53 | 13 | 66 |
2017 September | 50 | 16 | 66 |
2017 August | 39 | 15 | 54 |
2017 July | 37 | 9 | 46 |
2017 June | 47 | 11 | 58 |
2017 May | 44 | 14 | 58 |
2017 April | 42 | 9 | 51 |
2017 March | 27 | 10 | 37 |
2017 February | 36 | 25 | 61 |
2017 January | 20 | 20 | 40 |
2016 December | 76 | 7 | 83 |
2016 November | 88 | 16 | 104 |
2016 October | 101 | 12 | 113 |
2016 September | 150 | 4 | 154 |
2016 August | 233 | 15 | 248 |
2016 July | 226 | 14 | 240 |
2016 June | 147 | 0 | 147 |
2016 May | 139 | 0 | 139 |
2016 April | 118 | 0 | 118 |
2016 March | 114 | 0 | 114 |
2016 February | 142 | 0 | 142 |
2016 January | 157 | 0 | 157 |
2015 December | 148 | 0 | 148 |
2015 November | 116 | 0 | 116 |
2015 October | 96 | 0 | 96 |
2015 September | 78 | 0 | 78 |
2015 August | 82 | 0 | 82 |
2015 July | 83 | 0 | 83 |
2015 June | 26 | 0 | 26 |
2015 May | 67 | 0 | 67 |
2015 April | 12 | 0 | 12 |