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1.
J Nephrol ; 37(2): 365-378, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38123835

ABSTRACT

INTRODUCTION: In March 2020, a pandemic state was declared due to SARS-COV-2 (COVID-19). Patients with kidney disease, especially those on replacement therapies, proved more susceptible to severe infection. This rapid literature review aims to help understand how the pandemic impacted patient experience of kidney care. METHODS: It was conducted in accordance with Cochrane Rapid Review interim guidance. Search terms, 'coronavirus', 'kidney care', and 'patient-reported experience' and terms with similar semantic meaning, identified 1,117 articles in Medline, Scopus, and Worldwide Science. Seventeen were included in the narrative synthesis. RESULTS: The findings were summarised into three themes: remote consultation and telemedicine (n = 9); psychosocial impact (n = 2); and patient satisfaction and patient-reported experience (n = 6). Patients were mostly satisfied with remote consultations, describing them as convenient and allowing avoidance of hospital visits. Anxieties included missing potentially important clinical findings due to lack of physical examination, poor digital literacy, and technical difficulties. Psychosocial impact differed between treatment modalities-transplant recipients expressing feelings of instability and dread of having to return to dialysis, and generally, were less satisfied, citing reduced ability to work and difficulty accessing medications. Those on home dialysis treatments tended to feel safer. Findings focused on aspects of patient experience of kidney care during the pandemic rather than a holistic view. CONCLUSIONS: There was little direct evaluation of modality differences and limited consideration of health inequalities in care experiences. A fuller understanding of these issues would guide policy agendas to support patient experience during future public health crises.


Subject(s)
COVID-19 , Patient Satisfaction , Telemedicine , Humans , COVID-19/epidemiology , COVID-19/psychology , Kidney Diseases/therapy , Kidney Diseases/psychology , Kidney Transplantation , Remote Consultation
2.
Clin J Am Soc Nephrol ; 18(11): 1510-1518, 2023 11 01.
Article in English | MEDLINE | ID: mdl-37294578

ABSTRACT

Despite a large number of people globally being affected by rare kidney diseases, research support and health care policy programs usually focus on the management of the broad spectrum of CKD without particular attention to rare causes that would require a targeted approach for proper cure. Hence, specific curative approaches for rare kidney diseases are scarce, and these diseases are not treated optimally, with implications on the patients' health and quality of life, on the cost for the health care system, and society. There is therefore a need for rare kidney diseases and their mechanisms to receive the appropriate scientific, political, and policy attention to develop specific corrective approaches. A wide range of policies are required to address the various challenges that target care for rare kidney diseases, including the need to increase awareness, improve and accelerate diagnosis, support and implement therapeutic advances, and inform the management of the diseases. In this article, we provide specific policy recommendations to address the challenges hindering the provision of targeted care for rare kidney diseases, focusing on awareness and prioritization, diagnosis, management, and therapeutic innovation. In combination, the recommendations provide a holistic approach aiming for all aspects of rare kidney disease care to improve health outcomes, reduce the economic effect, and deliver benefits to society. Greater commitment from all the key stakeholders is now needed, and a central role should be assigned to patients with rare kidney disease to partner in the design and implementation of potential solutions.


Subject(s)
Kidney Diseases , Quality of Life , Humans , Delivery of Health Care , Health Policy , Kidney Diseases/diagnosis , Kidney Diseases/therapy
3.
Curr Opin Nephrol Hypertens ; 32(1): 41-48, 2023 01 01.
Article in English | MEDLINE | ID: mdl-36250456

ABSTRACT

PURPOSE OF REVIEW: Paediatric kidney disease results in considerable burden on children and their families. Paediatric palliative care is a holistic, family-centred care approach intended to enable flourishing and address the many impediments to life participation which advanced kidney disease can impose. To date, palliative care resources have been underutilized in paediatric nephrology. This review will highlight recent literature targeting the engagement and life participation of children with advanced kidney disease through implementation of novel palliative care approaches and propose directions for future research. RECENT FINDINGS: Children with advanced kidney disease and their families highly value incorporation of their perspectives, particularly on life participation, within care plan development; but what it means to participate in life can be variable, and clinicians need improved tools to ascertain and incorporate these perspectives. Novel palliative care interventions developed for application in comparable disease states offer potential opportunities for paediatric nephrologists to support this goal. SUMMARY: Children with advanced kidney disease and their families will benefit from incorporation of their perspectives and values, facilitated by palliative interventions.


Subject(s)
Kidney Diseases , Nephrology , Palliative Medicine , Child , Humans , Palliative Care/methods , Kidney Diseases/diagnosis , Kidney Diseases/therapy
4.
Clin J Am Soc Nephrol ; 17(1): 38-52, 2022 01.
Article in English | MEDLINE | ID: mdl-34980675

ABSTRACT

BACKGROUND AND OBJECTIVES: Nutrition intervention is an essential component of kidney disease management. This study aimed to understand current global availability and capacity of kidney nutrition care services, interdisciplinary communication, and availability of oral nutrition supplements. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: The International Society of Renal Nutrition and Metabolism (ISRNM), working in partnership with the International Society of Nephrology (ISN) Global Kidney Health Atlas Committee, developed this Global Kidney Nutrition Care Atlas. An electronic survey was administered among key kidney care stakeholders through 182 ISN-affiliated countries between July and September 2018. RESULTS: Overall, 160 of 182 countries (88%) responded, of which 155 countries (97%) answered the survey items related to kidney nutrition care. Only 48% of the 155 countries have dietitians/renal dietitians to provide this specialized service. Dietary counseling, provided by a person trained in nutrition, was generally not available in 65% of low-/lower middle-income countries and "never" available in 23% of low-income countries. Forty-one percent of the countries did not provide formal assessment of nutrition status for kidney nutrition care. The availability of oral nutrition supplements varied globally and, mostly, were not freely available in low-/lower middle-income countries for both inpatient and outpatient settings. Dietitians and nephrologists only communicated "sometimes" on kidney nutrition care in ≥60% of countries globally. CONCLUSIONS: This survey reveals significant gaps in global kidney nutrition care service capacity, availability, cost coverage, and deficiencies in interdisciplinary communication on kidney nutrition care delivery, especially in lower-income countries.


Subject(s)
Dietary Supplements , Kidney Diseases/therapy , Nutrition Therapy , Cross-Sectional Studies , Global Health , Health Care Surveys , Humans
5.
Toxins (Basel) ; 13(8)2021 08 17.
Article in English | MEDLINE | ID: mdl-34437444

ABSTRACT

Uremic toxins (UTs) are mainly produced by protein metabolized by the intestinal microbiota and converted in the liver or by mitochondria or other enzymes. The accumulation of UTs can damage the intestinal barrier integrity and cause vascular damage and progressive kidney damage. Together, these factors lead to metabolic imbalances, which in turn increase oxidative stress and inflammation and then produce uremia that affects many organs and causes diseases including renal fibrosis, vascular disease, and renal osteodystrophy. This article is based on the theory of the intestinal-renal axis, from bench to bedside, and it discusses nonextracorporeal therapies for UTs, which are classified into three categories: medication, diet and supplement therapy, and complementary and alternative medicine (CAM) and other therapies. The effects of medications such as AST-120 and meclofenamate are described. Diet and supplement therapies include plant-based diet, very low-protein diet, probiotics, prebiotics, synbiotics, and nutraceuticals. The research status of Chinese herbal medicine is discussed for CAM and other therapies. This review can provide some treatment recommendations for the reduction of UTs in patients with chronic kidney disease.


Subject(s)
Kidney Diseases/drug therapy , Kidney Diseases/therapy , Probiotics/therapeutic use , Uremia/chemically induced , Uremia/therapy , Uremic Toxins/toxicity , Adult , Aged , Aged, 80 and over , Complementary Therapies/methods , Diet Therapy/methods , Dietary Supplements , Female , Humans , Kidney Diseases/physiopathology , Male , Middle Aged , Renal Replacement Therapy/methods
6.
Int J Mol Sci ; 22(12)2021 Jun 20.
Article in English | MEDLINE | ID: mdl-34202940

ABSTRACT

Acute kidney injury (AKI) and chronic kidney disease (CKD) are rising in global prevalence and cause significant morbidity for patients. Current treatments are limited to slowing instead of stabilising or reversing disease progression. In this review, we describe mesenchymal stem cells (MSCs) and their constituents, extracellular vesicles (EVs) as being a novel therapeutic for CKD. MSC-derived EVs (MSC-EVs) are membrane-enclosed particles, including exosomes, which carry genetic information that mimics the phenotype of their cell of origin. MSC-EVs deliver their cargo of mRNA, miRNA, cytokines, and growth factors to target cells as a form of paracrine communication. This genetically reprograms pathophysiological pathways, which are upregulated in renal failure. Since the method of exosome preparation significantly affects the quality and function of MSC-exosomes, this review compares the methodologies for isolating exosomes from MSCs and their role in tissue regeneration. More specifically, it summarises the therapeutic efficacy of MSC-EVs in 60 preclinical animal models of AKI and CKD and the cargo of biomolecules they deliver. MSC-EVs promote tubular proliferation and angiogenesis, and inhibit apoptosis, oxidative stress, inflammation, the epithelial-to-mesenchymal transition, and fibrosis, to alleviate AKI and CKD. By reprogramming these pathophysiological pathways, MSC-EVs can slow or even reverse the progression of AKI to CKD, and therefore offer potential to transform clinical practice.


Subject(s)
Biological Therapy , Extracellular Vesicles/metabolism , Extracellular Vesicles/transplantation , Kidney Diseases/therapy , Mesenchymal Stem Cells/metabolism , Acute Kidney Injury/diagnosis , Acute Kidney Injury/etiology , Acute Kidney Injury/metabolism , Acute Kidney Injury/therapy , Animals , Apoptosis/drug effects , Biological Therapy/methods , Cell Differentiation , Cell Proliferation/drug effects , Cell Self Renewal , Chemical Fractionation , Disease Management , Disease Susceptibility , Exosomes/metabolism , Humans , Kidney Diseases/etiology , Kidney Diseases/pathology , Mesenchymal Stem Cells/cytology , Protective Agents , Renal Insufficiency/diagnosis , Renal Insufficiency/etiology , Renal Insufficiency, Chronic/diagnosis , Renal Insufficiency, Chronic/etiology , Renal Insufficiency, Chronic/metabolism , Renal Insufficiency, Chronic/therapy
8.
Transplantation ; 105(10): e114-e130, 2021 10 01.
Article in English | MEDLINE | ID: mdl-33982910

ABSTRACT

Interstitial fibrosis with tubule atrophy (IF/TA) is the response to virtually any sustained kidney injury and correlates inversely with kidney function and allograft survival. IF/TA is driven by various pathways that include hypoxia, renin-angiotensin-aldosterone system, transforming growth factor-ß signaling, cellular rejection, inflammation, and others. In this review, we will focus on key pathways in the progress of renal fibrosis, diagnosis and therapy of allograft fibrosis. This review discusses the role and origin of myofibroblasts as matrix producing cells and therapeutic targets in renal fibrosis with a particular focus on renal allografts. We summarize current trends to use multiomic approaches to identify new biomarkers for IF/TA detection and to predict allograft survival. Furthermore, we review current imaging strategies that might help to identify and follow-up IF/TA complementary or as alternative to invasive biopsies. We further discuss current clinical trials and therapeutic strategies to treat kidney fibrosis.


Subject(s)
Diet, Healthy , Graft Survival/drug effects , Kidney Diseases/diagnosis , Kidney Diseases/therapy , Kidney Transplantation/adverse effects , Kidney Tubules/drug effects , RNAi Therapeutics , Renal Agents/therapeutic use , Animals , Atrophy , Biomarkers/metabolism , Biopsy , Fibrosis , Humans , Immunosuppressive Agents/adverse effects , Kidney Diseases/etiology , Kidney Diseases/metabolism , Kidney Tubules/diagnostic imaging , Kidney Tubules/metabolism , Kidney Tubules/pathology , Predictive Value of Tests , RNAi Therapeutics/adverse effects , Renal Agents/adverse effects , Risk Factors , Signal Transduction , Treatment Outcome
9.
Nat Rev Nephrol ; 17(1): 15-32, 2021 01.
Article in English | MEDLINE | ID: mdl-33188362

ABSTRACT

Globally, more than 5 million people die annually from lack of access to critical treatments for kidney disease - by 2040, chronic kidney disease is projected to be the fifth leading cause of death worldwide. Kidney diseases are particularly challenging to tackle because they are pathologically diverse and are often asymptomatic. As such, kidney disease is often diagnosed late, and the global burden of kidney disease continues to be underappreciated. When kidney disease is not detected and treated early, patient care requires specialized resources that drive up cost, place many people at risk of catastrophic health expenditure and pose high opportunity costs for health systems. Prevention of kidney disease is highly cost-effective but requires a multisectoral holistic approach. Each Sustainable Development Goal (SDG) has the potential to impact kidney disease risk or improve early diagnosis and treatment, and thus reduce the need for high-cost care. All countries have agreed to strive to achieve the SDGs, but progress is disjointed and uneven among and within countries. The six SDG Transformations framework can be used to examine SDGs with relevance to kidney health that require attention and reveal inter-linkages among the SDGs that should accelerate progress.


Subject(s)
Health Services Accessibility , Kidney Diseases/prevention & control , Kidney Diseases/therapy , Nephrology , Renal Replacement Therapy , Sustainable Development , Catastrophic Illness/economics , Early Diagnosis , Early Medical Intervention , Education , Gender Equity , Health Expenditures , Humans , Kidney Diseases/economics , Poverty , Risk Reduction Behavior , Social Determinants of Health , Universal Health Care , Violence
10.
Pak J Pharm Sci ; 33(3): 1163-1167, 2020 May.
Article in English | MEDLINE | ID: mdl-33191243

ABSTRACT

Methotrexate (MTX) is a highly renal and liver toxicity drug used in hematological malignancy treatment in children and adults. High-dose methotrexate (HD-MTX) therapy may cause impairment of kidney and decrease the elimination of MTX, at the same time, the serum concentration of MTX increased. Today the treatment for preventing MTX toxicity after renal shutdown is Carboxypeptidase. We report a patient who experienced nephrotoxicity after the HD-MTX infusions during the treatment for non-Hodgkin lymphoma (NHL) and received hemodiafiltration (HDF) with large dose of leucovorin (LV) to treat MTX intoxication. LV is very potent in the prevention of neurotoxicity and administration of LV could protect the normal cells, but the dosage and duration of LV should be according to the MTX concentration. Although a large dose of LV was applied, the patient's condition did not improve. It was found that the HDF with large dose of LV to save the patient and steadily improved the patient's clinical condition.


Subject(s)
Antimetabolites, Antineoplastic/adverse effects , Hemodiafiltration , Kidney Diseases/therapy , Lymphoma, Non-Hodgkin/drug therapy , Methotrexate/adverse effects , Antidotes/therapeutic use , Humans , Kidney Diseases/blood , Kidney Diseases/chemically induced , Kidney Diseases/diagnosis , Leucovorin/therapeutic use , Male , Treatment Outcome , Young Adult
11.
Nutrients ; 12(11)2020 Nov 01.
Article in English | MEDLINE | ID: mdl-33139659

ABSTRACT

L-carnitine is an important factor in fatty acid metabolism, and carnitine deficiency is common in dialysis patients. This study evaluated whether L-carnitine supplementation improved muscle spasm, cardiac function, and renal anemia in dialysis patients. Eighty Japanese outpatients (62 hemodialysis (HD) patients and 18 peritoneal dialysis (PD) patients) received oral L-carnitine (600 mg/day) for 12 months; the HD patients further received intravenous L-carnitine injections (1000 mg three times/week) for 12 months, amounting to 24 months of treatment. Muscle spasm incidence was assessed using a questionnaire, and cardiac function was assessed using echocardiography. Baseline free carnitine concentrations were relatively low in patients who underwent dialysis for >4 years. Total carnitine serum concentration, free carnitine, and acylcarnitine significantly increased after oral L-carnitine treatment for 12 months, and after intravenous L-carnitine injection. There was no significant improvement in muscle spasms, although decreased muscle cramping after L-carnitine treatment was reported by 31% of patients who had undergone HD for >4 years. Hemoglobin concentrations increased significantly at 12 and 24 months in the HD group. Therefore, L-carnitine may be effective for reducing muscle cramping and improving hemoglobin levels in dialysis patients, especially those who have been undergoing dialysis for >4 years.


Subject(s)
Carnitine/administration & dosage , Dietary Supplements , Kidney Diseases/therapy , Peritoneal Dialysis/adverse effects , Renal Dialysis/adverse effects , Anemia/etiology , Anemia/therapy , Cardiomyopathies/etiology , Cardiomyopathies/therapy , Carnitine/deficiency , Female , Heart/physiopathology , Humans , Hyperammonemia/etiology , Hyperammonemia/therapy , Japan , Kidney Diseases/etiology , Male , Middle Aged , Muscular Diseases/etiology , Muscular Diseases/therapy , Prospective Studies , Spasm/etiology , Spasm/therapy , Treatment Outcome
12.
Clin J Am Soc Nephrol ; 15(9): 1259-1266, 2020 09 07.
Article in English | MEDLINE | ID: mdl-32665227

ABSTRACT

BACKGROUND AND OBJECTIVES: During the coronavirus disease 2019 outbreak, the treatment of families with children on long-term KRT is challenging. This study was conducted to identify the current difficulties, worries regarding the next 2 months, and mental distress experienced by families with children on long-term KRT during the coronavirus disease 2019 outbreak and to deliver possible management approaches to ensure uninterrupted treatment for children on long-term KRT. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A multicenter online survey was conducted between February 10 and 15, 2020, among the families with children on long-term KRT from five major pediatric dialysis centers in mainland China. The primary caregivers of children currently on long-term KRT were eligible and included. Demographic information, severe acute respiratory syndrome coronavirus 2 infection status, current difficulties, and worries regarding the next 2 months were surveyed using a self-developed questionnaire. The Patient Health Questionnaire-9 and the General Anxiety Disorder Scale-7 were used to screen for depressive symptoms and anxiety, respectively. RESULTS: Among the children in the 220 families included in data analysis, 113 (51%) children were on dialysis, and the other 107 (49%) had kidney transplants. No families reported confirmed or suspected cases of coronavirus disease 2019. Overall, 135 (61%) and 173 (79%) caregivers reported having difficulties now and having worries regarding the next 2 months, respectively. Dialysis supply shortage (dialysis group) and hard to have blood tests (kidney transplantation group) were most commonly reported. A total of 29 (13%) caregivers had depressive symptoms, and 24 (11%) had anxiety. After the survey, we offered online and offline interventions to address their problems. At the time of the submission of this paper, no treatment interruption had been reported. CONCLUSIONS: The coronavirus disease 2019 outbreak has had physical, mental, logistical, and financial effects on families with children on long-term KRT.


Subject(s)
Betacoronavirus/pathogenicity , Coronavirus Infections/prevention & control , Family/psychology , Kidney Diseases/therapy , Pandemics/prevention & control , Pneumonia, Viral/prevention & control , Renal Replacement Therapy , Adaptation, Psychological , Adolescent , Adult , Age Factors , COVID-19 , Caregivers/psychology , Child , China/epidemiology , Coronavirus Infections/psychology , Coronavirus Infections/transmission , Coronavirus Infections/virology , Cost of Illness , Family Relations , Female , Health Care Surveys , Health Knowledge, Attitudes, Practice , Health Services Accessibility , Host Microbial Interactions , Humans , Kidney Diseases/psychology , Male , Mental Health , Middle Aged , Patient Safety , Pneumonia, Viral/psychology , Pneumonia, Viral/transmission , Pneumonia, Viral/virology , Renal Replacement Therapy/adverse effects , Risk Assessment , Risk Factors , SARS-CoV-2 , Time Factors , Treatment Outcome
13.
J Hypertens ; 38(9): 1849-1856, 2020 09.
Article in English | MEDLINE | ID: mdl-32649620

ABSTRACT

BACKGROUND: Uncontrolled hypertension notwithstanding the use of at least three drugs or hypertension controlled with at least four drugs, the widely accepted definition of treatment-resistant hypertension (TRH), is considered as a common problem in the hemodialysis population. However, to date there is no estimate of the prevalence of this condition in hemodialysis patients. METHOD: We estimated the prevalence of TRH by 44-h ambulatory BP monitoring (ABPM) in 506 hemodialysis patients in 10 renal units in Europe included in the registry of the European Renal and Cardiovascular Medicine (EURECAm,), a working group of the European Association, European Dialysis and Transplantation Association (ERA EDTA). In a sub-group of 114 patients, we tested the relationship between fluid overload (Body Composition monitor) and TRH. RESULTS: The prevalence of hypertension with 44-h ABPM criteria was estimated at 85.6% (434 out of 506 patients). Of these, 296 (58%) patients were classified as uncontrolled hypertensive patients by 44-h ABPM criteria (≥130/80 mmHg). Two hundred and thirteen patients had uncontrolled hypertension while on treatment with less than three drugs and 210 patients were normotensive while on drug therapy (n = 138) or off drug treatment (n = 72). The prevalence of TRH was 24% (93 among 386 treated hypertensive patients). The prevalence of predialysis fluid overload was 33% among TRH patients, 34% in uncontrolled hypertensive patients and 26% in normotensive patients. The vast majority (67%) of hemodialysis patients with TRH had no fluid overload. CONCLUSION: TRH occurs in about one in four treated hypertensive patients on hemodialysis. Fluid overload per se only in part explains TRH and the 67% of these patients show no fluid overload.


Subject(s)
Blood Pressure Monitoring, Ambulatory , Hypertension , Kidney Diseases , Renal Dialysis , Humans , Hypertension/complications , Hypertension/diagnosis , Hypertension/epidemiology , Kidney Diseases/complications , Kidney Diseases/epidemiology , Kidney Diseases/therapy , Prevalence
14.
Nutr Metab Cardiovasc Dis ; 30(8): 1382-1388, 2020 07 24.
Article in English | MEDLINE | ID: mdl-32513581

ABSTRACT

BACKGROUND AND AIM: Lipid abnormalities are common in peritoneal dialysis (PD) patients and no effective treatment to decrease serum lipoprotein (a) [Lp(a)] in dialysis patients is known so far. Therefore, this research was designed to investigate the effects of soy isoflavone supplement on serum lipids and Lp(a) in PD patients. METHODS & RESULTS: In this randomized, double-blind, placebo-controlled trial, 40 PD patients were randomly assigned to either the isoflavone or the placebo group. The patients in the isoflavone group received 100 mg soy isoflavone daily for 8 weeks, whereas the placebo group received corresponding placebos. At baseline and the end of the 8th week, 7 mL of blood was obtained from each patient and serum triglycerides, total cholesterol, low density lipoprotein-cholesterol (LDL-C), high density lipoprotein-cholesterol (HDL-C), and Lp(a) were measured. Serum Lp(a) reduced significantly up to 10% in the isoflavone group at the end of week 8 compared to baseline (P < 0.05), and the reduction was significant in comparison with the placebo group (P < 0.05). Serum HDL-C increased significantly up to 11.5% in the isoflavone group at the end of week 8 compared to baseline (P = 0.05), and the increment was significant in comparison with the placebo group (P < 0.05). There were no significant differences between the two groups in mean changes of serum triglycerides, total cholesterol, and LDL-C. CONCLUSIONS: This study indicates that daily administration of 100 mg soy isoflavones reduces serum Lp(a) and increases HDL-C concentration which are two determinants of cardiovascular disease in PD patients. CLINICALTRIALS.GOV: NCT03773029. REGISTRATION NUMBER AND DATE: NCT03773029 - 2018.


Subject(s)
Cholesterol, HDL/blood , Dietary Supplements , Glycine max , Isoflavones/administration & dosage , Kidney Diseases/therapy , Lipoprotein(a)/blood , Peritoneal Dialysis, Continuous Ambulatory , Biomarkers/blood , Dietary Supplements/adverse effects , Double-Blind Method , Female , Humans , Iran , Isoflavones/adverse effects , Isoflavones/isolation & purification , Kidney Diseases/blood , Kidney Diseases/diagnosis , Male , Middle Aged , Peritoneal Dialysis, Continuous Ambulatory/adverse effects , Glycine max/chemistry , Time Factors , Treatment Outcome
15.
Biosci Rep ; 40(6)2020 06 26.
Article in English | MEDLINE | ID: mdl-32490516

ABSTRACT

The improvement of malnutrition with levocarnitine in maintenance hemodialysis (MHD) patients is controversial. We performed a meta-analysis to evaluate the efficacy of levocarnitine in improving malnutrition in MHD patients. We performed a literature search for relevant articles related to the treatment of malnutrition by L-carnitine in MHD patients in PubMed, Embase, Web of Science, China National Knowledge Infrastructure, and Wanfang databases. We set the publication dates from 1950 to July 2019. The levels of albumin, prealbumin, total protein, and transferrin before and after treatment were used for assessing malnutrition. Twenty-seven studies were included in the present analysis. The results of the random effects model indicated that L-carnitine treatment improved the albumin level in patients on MHD patients. The pooled standardized mean difference of albumin level was 2.51 (95% confidence interval (CI): 2.13-2.90, P<0.001). The pooled total protein level was 3.83 (95% CI: 2.41-5.24, P = 0.000) and the pooled transferrin level was 0.35 (95% CI: 0.18-0.52, P = 0.000). Significant differences were observed with the total protein and transferrin levels. The results indicated that levocarnitine significantly improved the prealbumin level in patients on MHD. The pooled prealbumin level was 70.86 (95% CI: 42.99-98.73, P = 0.000). No publication bias was detected (P>0.05). The present meta-analysis indicated that L-carnitine can have a favorable effect on malnutrition biomarkers in patients on MHD, including the increase in albumin, total protein, transferrin, and prealbumin levels. The L-carnitine could be an option for treatment of MHD patients.


Subject(s)
Carnitine/therapeutic use , Dietary Supplements , Kidney Diseases/therapy , Malnutrition/drug therapy , Nutritional Status , Renal Dialysis , Adult , Aged , Aged, 80 and over , Biomarkers/blood , Carnitine/adverse effects , Dietary Supplements/adverse effects , Female , Humans , Kidney Diseases/complications , Kidney Diseases/diagnosis , Male , Malnutrition/diagnosis , Malnutrition/etiology , Malnutrition/physiopathology , Middle Aged , Prealbumin/metabolism , Renal Dialysis/adverse effects , Serum Albumin, Human/metabolism , Transferrin/metabolism , Treatment Outcome
17.
Clin J Am Soc Nephrol ; 15(4): 511-520, 2020 04 07.
Article in English | MEDLINE | ID: mdl-32188636

ABSTRACT

BACKGROUND AND OBJECTIVES: Compared with hemodialysis, home peritoneal dialysis alleviates the burden of travel, facilitates independence, and is less costly. Physical, cognitive, or psychosocial factors may preclude peritoneal dialysis in otherwise eligible patients. Assisted peritoneal dialysis, where trained personnel assist with home peritoneal dialysis, may be an option, but the optimal model is unknown. The objective of this work is to characterize existing assisted peritoneal dialysis models and synthesize clinical outcomes. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A systematic review of MEDLINE, Cochrane Central Register of Controlled Trails, Cochrane Database of Systematic Reviews, Embase, PsycINFO, and CINAHL was conducted (search dates: January 1995-September 2018). A focused gray literature search was also completed, limited to developed nations. Included studies focused on home-based assisted peritoneal dialysis; studies with the assist provided exclusively by unpaid family caregivers were excluded. All outcomes were narratively synthesized; quantitative outcomes were graphically depicted. RESULTS: We included 34 studies, totaling 46,597 patients, with assisted peritoneal dialysis programs identified in 20 jurisdictions. Two categories emerged for models of assisted peritoneal dialysis on the basis of type of assistance: health care and non-health care professional assistance. Reported outcomes were heterogeneous, ranging from patient-level outcomes of survival, to resource use and transfer to hemodialysis; however, the comparative effect of assisted peritoneal dialysis was unclear. In two qualitative studies examining the patient experience, the maintenance of independence was identified as an important theme. CONCLUSIONS: Reported outcomes and quality were heterogeneous, and relative efficacy of assisted peritoneal dialysis could not be determined from included studies. Although the patient voice was under-represented, suggestions to improve assisted peritoneal dialysis included using a person-centered model of care, ensuring continuity of nurses providing the peritoneal dialysis assist, and measures to support patient independence. Although attractive elements of assisted peritoneal dialysis are identified, further evidence is needed to connect assisted peritoneal dialysis outcomes with programmatic features and their associated funding models.


Subject(s)
Delivery of Health Care, Integrated/organization & administration , Home Care Services/organization & administration , Kidney Diseases/therapy , Models, Organizational , Peritoneal Dialysis , Caregivers/organization & administration , Continuity of Patient Care/organization & administration , Health Personnel/organization & administration , Humans , Kidney Diseases/diagnosis , Kidney Diseases/physiopathology , Patient Satisfaction , Patient-Centered Care/organization & administration , Peritoneal Dialysis/adverse effects , Quality of Life , Treatment Outcome
18.
Hum Exp Toxicol ; 39(6): 855-869, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32003233

ABSTRACT

The current study was aimed at exploring the protective efficacy of spirulina against the hemato-biochemical alterations and nephrotoxicity induced by lead (Pb). Female rats aged 12 weeks were treated for 4 weeks with Pb (0.344 g kg-1 bw) associated or not with spirulina (5.3 g kg-1 bw). Renal damage induced by Pb was related to a severe anemia, increases of oxidative stress-related parameters (thiobarbituric acid reactive substances (TBARS) (+29%), protein carbonyl (PCO) (+66.3%), and advanced oxidation protein product (AOPP) (+110%)), plasma lactate dehydrogenase (LDH) (+80%), creatinine and urea levels in plasma, and uric acid concentration in urine, as well as genotoxic changes (+89.3% and +60% for DNA and mRNA levels, respectively). Conversely, LDH and antioxidant enzyme activities in kidney were decreased, as well as the levels of plasma uric acid, and urinary creatinine and urea levels. Spirulina-supplemented rats exhibited normal peripheral blood and renal parameters and renal histology. It can be suggested that Arthrospira platensis alleviates damages induced by Pb, thanks to its high phenolic content and antioxidant capacity.


Subject(s)
Kidney Diseases/therapy , Organometallic Compounds/toxicity , Protective Agents/therapeutic use , Spirulina , Animals , Creatinine/blood , Creatinine/urine , DNA/metabolism , DNA Damage , Female , Hematologic Tests , Kidney/drug effects , Kidney/metabolism , Kidney/pathology , Kidney Diseases/chemically induced , Kidney Diseases/metabolism , Kidney Diseases/pathology , Oxidative Stress/drug effects , RNA, Messenger/metabolism , Rats, Wistar , Thiobarbituric Acid Reactive Substances/metabolism , Urea/blood , Urea/urine , Uric Acid/blood , Uric Acid/urine
19.
BMC Cardiovasc Disord ; 20(1): 39, 2020 01 30.
Article in English | MEDLINE | ID: mdl-32000687

ABSTRACT

BACKGROUND: Although mineral metabolism disorder influences cardiac valvular calcification (CVC), few previous studies have examined the effects of non-calcium-containing and calcium-containing phosphate binders on CVC in maintenance hemodialysis patients. The aim of the present study was to compare the effects of lanthanum carbonate (LC) with calcium carbonate (CC) on the progression of CVC in patients who initiated maintenance hemodialysis and to investigate clinical factors related to CVC. METHODS: The current study included 50 subjects (mean age 65 years, 72% males) from our previous randomized controlled trial (LC group, N = 24; CC group, N = 26). CVC was evaluated as CVC score (CVCS) using echocardiography at baseline and 18 months after initiation of hemodialysis. We compared CVCS and the changes between the two groups. We also analyzed the associations between CVCS and any other clinical factors including arterial plaque score (PS) and serum phosphorus levels. RESULTS: Baseline characteristics of study participants including CVCS were almost comparable between the two groups. At 18 months, there were no significant differences in mineral metabolic markers or CVCS between the two groups, and CVCS were significantly correlated with PS (r = 0.39, p < 0.01). Furthermore, changes in CVCS were significantly correlated with average phosphorus levels (r = 0.36, p < 0.05), which were significantly higher in high serum phosphorus and high PS group compared to low serum phosphorus and low PS group (p < 0.05). CONCLUSIONS: In the present study, there were no significant differences between LC and CC with regard to progression of CVC. However, serum phosphorus levels and arterial plaque seem to be important for the progression and formation of CVC in hemodialysis patients.


Subject(s)
Calcinosis/prevention & control , Calcium Carbonate/therapeutic use , Chelating Agents/therapeutic use , Heart Valve Diseases/prevention & control , Kidney Diseases/therapy , Lanthanum/therapeutic use , Renal Dialysis , Aged , Aged, 80 and over , Biomarkers/blood , Calcinosis/blood , Calcinosis/diagnostic imaging , Calcinosis/etiology , Calcium Carbonate/adverse effects , Chelating Agents/adverse effects , Disease Progression , Female , Heart Valve Diseases/blood , Heart Valve Diseases/diagnostic imaging , Heart Valve Diseases/etiology , Humans , Kidney Diseases/blood , Kidney Diseases/complications , Kidney Diseases/diagnosis , Lanthanum/adverse effects , Male , Middle Aged , Phosphorus/blood , Randomized Controlled Trials as Topic , Renal Dialysis/adverse effects , Risk Factors , Time Factors , Treatment Outcome
20.
Nutrition ; 72: 110664, 2020 04.
Article in English | MEDLINE | ID: mdl-31972420

ABSTRACT

Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations in the GLA gene that result in deficiency of enzyme α-galactosidase A activity. Clinical manifestation varies from mild to severe depending on the phenotype. The main clinical manifestations are cutaneous (angiokeratomas), neurologic (acroparesthesias), gastrointestinal (nausea, diarrhea, and abdominal pain), renal (proteinuria and kidney failure), cardiovascular (cardiomyopathy and arrhythmias), and cerebrovascular (stroke). Enzyme replacement therapy with recombinant human α-galactosidase is currently the therapeutic option for FD. Although enzyme replacement therapy has changed the natural history of disease, many clinical aspects of FD require an additional specific treatment. Nutritional approach is mostly indicated in case of nephropathy and gastrointestinal symptoms. Specific dietary interventions can modulate some pathogenetic mechanisms of the disease, such as the inflammation, oxidative stress, and autophagic disorders. However, to our knowledge, limited attention has been given to the nutritional aspects of FD. The aim of this review is to examine nutritional strategies that might interfere with several pathophysiologic aspects of FD, including inflammation and oxidative stress. A dietary approach should be part of the basic treatment in renal manifestations of FD. Dietary measures recommended for irritable bowel syndrome could be recommended for gastrointestinal symptoms. Dietary factors can modulate the inflammation, oxidative stress, and autophagy involved in FD. Polyphenols, ω-3 fatty acids, microbiota, and specific dietary patterns can interfere with inflammation/oxidative stress and autophagy mechanisms and could also contribute to the slowing of FD progression.


Subject(s)
Enzyme Replacement Therapy/methods , Fabry Disease/therapy , Kidney Diseases/therapy , Nutrition Therapy/methods , Combined Modality Therapy , Fabry Disease/complications , Fabry Disease/physiopathology , Humans , Kidney/physiopathology , Kidney Diseases/genetics
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