Renal involvement and metabolic alterations in adults patients affected by cystic fibrosis

Cystic fibrosis (CF) is an autosomal recessive genetic disease, with a high prevalence in Europe, North America and Australia [1, 2], involving about between 1:2500 and 1:1800 people and it is therefore classified as one of the most frequent genetic diseases. The disease is caused by the mutation of the Cystic Fibrosis Transmembrane Regulator (CFTR) gene [1, 2] that maps on chromosome 7 and encodes the CFTR protein, which is a transmembrane channel of chlorine [3, 4]. This channel regulates the transport of anions and ciliary mucus clearance in lungs, its dysfunction then leads to mucosal retention, chronic pulmonary infections, inflammation and progressively to lung damage with respiratory failure [5, 6]. Cystic fibrosis is a systemic disease that affects the epithelial cells of the pancreas (85–90% of cases) causing malabsorption and pancreatic insufficiency [7‐9], the liver with biliary cirrhosis, male genital system causing atrophy and agenesis of the deferent ducts, then infertility [10, 11]. The increasing longevity among CF patients exposes them to the risk of developing nephropathy, this disease is known as CF related kidney disease (CFKD) [12, 13]. Renal involvement in CF may be associated with the underlying disease, with the comorbidities and with the treatment that patients receive. In fact the CFTR gene is expressed also in the kidneys, causing alterations in electrolyte homeostasis, but until now renal involvement has been little studied. In addition, comorbidities such as diabetes could cause nephropathy. However the most studied and known cause of renal injury in CF patients is iatrogenic, related to the intake of high doses of aminoglycosides (3–5 mg/kg/dose) during pulmonary exacerbations [14, 15]. Aminoglycosides are characterized by renal excretion through glomerular filtration, up to 15% is reabsorbed into the proximal tubule through a saturable mechanism, once overcome phenomena of cellular apoptosis occur, therefore presents a dose-dependent action. In the treatment of patients with CF the therapeutic dose is comparable to the toxic dose [16‐19]. With advances in the therapy of CF, life expectancy has increased, and some previously unobserved disease associations are now seen in patients with CF. The aim of this study is to evaluate the incidence, the manifestations of renal disease and the possible association with metabolic and endothelial dysfunction markers in the CF population.

The study protocol was approved by the Clinical Research Ethics Committee of Sapienza, University of Rome, Italy. The study conforms to the principles outlined in the Declaration of Helsinki and we obtained a written consent by each patient enrolled.

Patient’s characteristics are shown in Table 1. A total of 226 patients (126 males) with the average age of 34.92 ± 11.67 years were evaluated. We divided the population into three groups evaluating the eGFR and the FEV 1 (Tables 2, 3) and we showed that 65 patients (28.8%) (28 males) have a reduced value of eGFR < 90 mL/min/1.73 m² and 158 patients have a reduced value of FEV1, of which 58 patients (26%) (34 males) with a severe reduction of FEV1. Moreover we have stratified the population by the CFTR mutation classes and eGFR, confirming the prevalence of mutation class II with a major number of patients with reduced eGFR (Table 4). On a total of 226 patients, 28 had undergone lung transplantation, and we found that these patients had a significant lower eGFR with respect to the non-transplanted patients (p < 0.001) (Table 5), while we did not shown a significant difference in FEV1. Moreover we showed that eGFR and age are inversely proportional, but eGFR is significant lower in transplant patients compared to non-transplanted patients of the same age (p < 0.001) (Fig. 1). We reported also a significant association between lower eGFR value and serum triglyceride, total cholesterol and LDL (p = 0.005, p < 0.001, p = 0.040; respectively) (Table 6), with a significant negative correlation between eGFR and serum triglyceride (Fig. 2). Moreover we found a significant association between lower eGFR value and SUA (p = 0.005), while we did not found an association with 25-OH-VitD value, serum glucose and HbA1c (Table 6).

More than 2000 mutations of CFTR gene have been identified, the most frequent variation is ΔF508 (Class II), characterized by the deletion of three nucleotides with the loss of the codon coding for phenylalanine [4, 6]. This mutation involves the altered formation of the CFTR protein that is degraded by proteasomes in the endoplasmic reticulum, with a lack of exposure of the channel on the membrane. The various mutations are categorized into six classes [3] depending on the type of protein deficit which has been found. The effects of CF are not limited to the lung alone, although, the major cause of mortality is associated with bronchiectasis and subsequent infections. Early diagnosis, intensive antibiotic therapy and developments in supportive treatment have extended the life expectancy for CF patients by reducing mortality and morbidity. Due to the increase in patient lifespans, previously unobserved disease associations have been detected. Renal involvement in CF patients has always been considered rare, but recently, renal pathologies such as glomerulosclerosis, mesangial proliferation, membranoproliferative and postinfectious glomerulonephritis, nephrocalcinosis and hematuria, tubular damage, fibrillary glomerulonephritis, and amyloidosis, in particular amyloid protein A (AA) in children, have been reported [23]. There has been a dramatic increase in median survival of CF patients over the last two decades, in fact median survival has improved to 45 years, therefore it becomes necessary to deal with long-term complications such as renal and cardiovascular diseases. Acute kidney injury (AKI) in patients with CF is well documented in association with episodes of infection and use of antibiotics [18], while the prevalence and possible causes of CKD remains more debated. In our study we showed a prevalence of CKD of 28.8%, while another study [19] reported a prevalence of 14.2% of CKD with the same prevalent mutation (∆F508, class II). Moreover, in our study, we showed a reduced eGFR in lung transplanted patients with respect to the non-transplanted patients. Also Degen et al. [24] showed a worse renal function in transplanted patients, probably due to the use of immunosuppressive drugs such as cyclosporine and other calcineurin inhibitors. We reported also an increase of metabolic indexes, as triglycerides, total cholesterol and LDL, progression factors of renal damage and cardiovascular risk factors. The increase of serum triglycerides in patients with CKD is due to a dual mechanism, increased synthesis and reduced clearance [25], determining a lipid profile that favors atherosclerosis and consequent increase in cardiovascular risk. Moreover, we found an increase of SUA in patients with worse renal function. In recent years it has been shown that high levels of SUA are associated with renal and cardiovascular events, mainly due to renal glomerular vasoconstriction [26]. In a 7-year follow-up study of a sample of 177.570 individuals, patients with high SUA were found to have a 26% increased risk of developing CKD [27]. Hyperuricemia is involved in endothelial dysfunction by increasing inflammation and oxidative stress, however is unclear whether it is an individual risk factor or if it is associated with other risk factors such as hypertension, metabolic syndrome and CKD [28]. The integrity of the endothelium plays an important role in the maintenance of homeostasis by regulating the balance between vasoconstriction and vasodilation, in fact a possible mechanism of dysfunction related to SUA is given by the decoupling of xanthine-oxido-reductase and endothelial nitric-oxide-synthase (eNOS). Xanthine-oxido-reductase catalyzes the oxidative reaction of hypoxanthine in xanthine and finally in urate, in the metabolic process of purines. Xanthine-oxido-reductase exists in two forms, xanthine-dehydrogenase (XD) and xanthine-oxidase (XO), the former uses as NAD⁺ acceptor and NADH will be formed at the end of the conversion process. The XO instead uses molecular oxygen as an electron acceptor, at the end of the process anion peroxide and hydrogen peroxide will form. In a condition in which the XO is misused therefore, not only SUA, but also reactive oxygen species will have a deleterious effect on the endothelial component [29, 30]. According to the literature, 20% of adolescents and 40–50% of adults have CF related diabetes (CFRD), distinct from type 1 or type 2 diabetes [11]. In our study we showed higher levels of glycemia and HbA1c in patients with reduced eGFR even if not statistically significant. Cystic fibrosis related diabetes is the end-point of a spectrum of glucose abnormalities in CF that begins with early insulin deficiency and is associated with accelerated nutritional decline and deterioration of lung function [31]. Microvascular complications can occur, but the main cause of death is respiratory failure rather than cardiovascular causes as in type 1 or type 2 diabetes [32]. In our study we showed a reduced value of FEV1 in 158 patients (70.8%) even if we did not shown significant difference in patients with CKD and between transplanted and non-transplanted patients. Pulmonary function tests can yield measurements of lung capacity, forced expiratory flow, vital capacity and residual volume, but one of the most important spirometric parameter in CF is FEV1, an index of airway obstruction, that plays an important role in both clinical care and research [33]. The strong relationship between FEV1 and the pathophysiology of this chronic respiratory disease, combined with the ability to be objectively and reliably measured relatively to other endpoints, has made FEV1 a key endpoint to measure both efficacy and safety in CF clinical trials. There has been a dramatic increase in median survival of these patients in the last few years, but respiratory failure remains the leading cause of death among CF patients, and FEV1 remains an established marker of disease progression that can be used to evaluate the clinical course and therapeutic efficacy [33].

The limitations of our study are the limited sample size of CF patients, and the cross-sectional, single center study without control group. The limitation for all single-centre analysis is the potential lack of generalizability. Additional prospective follow-up studies with a larger number of patients are necessary to confirm our results.

Our study shows a high prevalence of CKD in CF patients. Moreover we showed an increase of endothelial dysfunction and dyslipidemia indexes in patients with reduced renal function, as SUA, serum triglycerides and LDL, suggesting the need for an early and complete screening of the main metabolic indexes to reduce cardiovascular risk and progression of renal damage. Furthermore, a careful and frequent evaluation of eGFR could be an important predictor and control factor for renal damage, especially in patients with lung transplantation.