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1.
Scand J Immunol ; 98(1): e13279, 2023 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-37133326

RESUMEN

The introduction of the Luminex Crossmatch assay (LumXm) which uses Luminex bead technology, consists of extracting the donor's Human Leukocyte Antigen (HLA) molecules from their lymphocytes, and binding them to fluorescent beads that are put in contact with recipient's serum. HLA donor-specific antibodies (DSA) are detected using a fluorescent conjugate. The goal of our study is to determine the benefits of using LumXm in a renal transplantation algorithm. We tested 78 recipients' sera using the LumXm, and the results were compared with the Luminex single antigen bead assay (SAB) for all sera, as well as the Flow Cytometry Crossmatch (FCXM) for 46 sera. We compared our results with those of SAB using 3 cutoffs, the first being the manufacturer's criteria where sensitivity and specificity were at 62.5% and 91.3% respectively for HLA class 1, and 88.5% and 50.0% respectively for HLA class 2. When using the third cutoff criteria (≥2 Adjusted values + MFI [Mean fluorescence intensity] >500 + Neg MFI < 500), the sensitivity increased to 69.0% for HLA class 1 and decreased to 84.0% for HLA class 2, while the specificity increased for HLA class 1 and 2. When comparing with FCXM, the 3 assays agreed in 55.8% of results for class 1 and 2 alike. However, major discrepancies were found for two groups in HLA class 1 and one in HLA class 2. The LumXm when used with other techniques to overcome its' weak points, can provide an interesting insight into the patient's HLA-DSA profile.


Asunto(s)
Trasplante de Riñón , Humanos , Anticuerpos , Antígenos HLA , Donantes de Tejidos , Prueba de Histocompatibilidad/métodos , Antígenos de Histocompatibilidad Clase II , Antígenos de Histocompatibilidad Clase I , Rechazo de Injerto/prevención & control
2.
Ren Fail ; 44(1): 1243-1262, 2022 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-35930297

RESUMEN

OBJECTIVES: Several studies have shown that cholecalciferol supplementation (25OHD-S) in chronic kidney disease (CKD) improves kidney injury by reducing fibrosis-related vascular calcification and declining apoptosis-linked nephron damage. METHODS: The oral 25OHD-S was evaluated in 60,000 IU/month/36 weeks versus in 2000 IU/d/24 weeks in CKD Stage 3 with serum 25OHD level < 20 ng/mL. The study was undertaken on 156 black subjects and 150 white subjects Southern Sahara (SS). All biomarkers of cardiometabolic (CMet) and cardiorenal (CRenal) syndrome, Renin-angiotensin-aldosterone system (RAAS) profile, secondary hyperparathyroidism (SHPT), N-terminal pro B-type natriuretic peptide (NT-proBNP), Troponin T (cTnT) and atherogenicity risk were assessed by biochemical methods. Estimate glomerular filtration rate (eGFR) by chronic CKD-EPI equation formula. Total serum vitamin D by liquid chromatography-tandem mass spectrometry (MS). RESULTS: Vitamin D deficiency alters in the same manner CMet, CRenal, and others biomarkers in both groups SS; however, these disorders are more acute in blacks compared to whites SS. Oral 25OHD-S a highlighted improvement of eGFR drop, SHPT decrease, decline proteinuria, and cardiac failure risk (NT-proBNP and cTnT) attenuation. Concomitantly, 25OHD-S normalizes Renin, Aldosterone, and Angiotensin System (RAAS) activity. Nevertheless, homocysteine and Lp (a) do not modulate by 25OHD-S. CONCLUSIONS: The oral vitamin D3 supplementation, according the dose, and the treatment duration does not like in black-skinned people versus to white-skinned inhabitants, while the 02 groups are native to the same Saharan environment. It emerge that a high intermittent dose through an extensive supplementation (60,000 IU/36 weeks) was more effective in black subjects. At opposite, a lower dose during a short period supplementation is sufficient (2000 IU/24 weeks) in white subjects.


Asunto(s)
Síndrome Cardiorrenal , Hiperparatiroidismo Secundario , Insuficiencia Renal Crónica , Deficiencia de Vitamina D , Biomarcadores , Síndrome Cardiorrenal/complicaciones , Síndrome Cardiorrenal/etnología , Síndrome Cardiorrenal/etiología , Colecalciferol/administración & dosificación , Colecalciferol/uso terapéutico , Suplementos Dietéticos , Humanos , Hiperparatiroidismo Secundario/complicaciones , Hiperparatiroidismo Secundario/etnología , Troponina T
3.
Tunis Med ; 102(7): 423-428, 2024 Jul 05.
Artículo en Francés | MEDLINE | ID: mdl-38982968

RESUMEN

INTRODUCTION: Chronic kidney disease (CKD) stage 5 is a common pathology, the increase in its incidence and prevalence has been noted worldwide. In Algeria, few studies have been done on the epidemiology of chronic kidney disease, the real extent of its incidence in southern Algeria remains unknown. AIM: To determine the incidence in 2017 of chronic kidney disease stage 5 treated by renal replacement in southeastern Algeria. METHOD: During our multicenter, prospective longitudinal regional study, from January 1, 2017 to December 31, 2017, all resident incident cases of CKD stage 5 treated in the region by renal replacement were recruited. RESULTS: The crude incidence of stage 5 CKD treated in 2017 in southeastern Algeria was 75 pmh. The age-standardized incidence rate was 100 pmh, with a male predominance, a M/F sex ratio of 1.59. The average age of incident cases was 48.50 ± 19.12 years. The incidence varies by age group and by wilaya. Diabetes (26.7%) and hypertensive nephropathy (22.6%) represent almost half of the cases and primary glomerulonephritis represents 5.9%. CONCLUSION: CKD stage 5 treated, due to its high incidence in Algeria, with large geographical variations, represents a major public health challenge. It mainly affects young people. Diabetes and high blood pressure represent the two main causes, encouraging prevention efforts to be focused on hypertensives and diabetics in high-risk wilayas.


Asunto(s)
Insuficiencia Renal Crónica , Humanos , Argelia/epidemiología , Masculino , Femenino , Incidencia , Persona de Mediana Edad , Adulto , Insuficiencia Renal Crónica/epidemiología , Anciano , Estudios Prospectivos , Adulto Joven , Adolescente , Estudios Longitudinales , Niño , Anciano de 80 o más Años , Preescolar , Terapia de Reemplazo Renal/estadística & datos numéricos , Hipertensión/epidemiología
4.
J Clin Med ; 12(12)2023 Jun 07.
Artículo en Inglés | MEDLINE | ID: mdl-37373595

RESUMEN

Kidney transplantation is a major risk factor for severe forms of coronavirus disease 2019 (COVID-19). The dynamics and the persistence of the immune response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in this immunocompromised population remain largely unknown. This study aimed to evaluate the persistence of humoral and cellular immune response in kidney transplant recipients (KTRs) and to establish whether immunosuppressive therapy influenced long-term immunity in this population. We report here the analysis of anti-SARS-CoV-2 antibodies and T cell-mediated immune responses in 36 KTRs compared to a control group who recovered from mild COVID-19. After a mean time of 5.22 ± 0.96 months post symptom onset for kidney transplant recipients, 97.22% of patients and 100% of the control group displayed anti-S1 immunoglobulin G SARS-CoV-2 antibodies (p > 0.05). No significant difference was reported in the median of neutralizing antibodies between the groups (97.50 [55.25-99] in KTRs vs. 84 [60-98] in control group, p = 0.35). A significant difference in SARS-CoV-2-specific T cell reactivity was found in the KTRs compared to the healthy controls. The levels of IFNγ release after stimulation by Ag1, Ag2 and Ag3 were higher in the control group compared to the kidney transplant group (p = 0.007, p = 0.025 and p = 0.008, respectively). No statistically significant correlation between humoral and cellular immunity was found in the KTRs. Our findings indicated that humoral immunity persisted similarly for up to 4 to 6 months post symptom onset in both the KTRs and the control group; however, T cell response was significantly higher in the healthy population compared to the immunocompromised patients.

5.
Nephrol Ther ; 19(1): 45-57, 2023 03 16.
Artículo en Francés | MEDLINE | ID: mdl-36919592

RESUMEN

Introduction: Chronic kidney disease stage V, by its incidence and its prevalence which are constantly increasing in the world and in Algeria, the morbidity and mortality it generates, the high cost of its treatment, represents a major public health issue. Our objective is to describe the epidemiology of stage V chronic kidney disease treated in south-eastern Algeria. Patients and methods: In our regional, multicenter, prospective descriptive study, all patients with stage V chronic kidney disease, residing and treated in south-eastern Algeria between September 1, 2016, and December 31, 2017, were included and followed up until December 31, 2018. Results: Stage V chronic kidney disease is a frequent pathology in the region: 1934 patients were included. It mainly affects young people: the average age of patients was 50.17 ± 16.98 years, with a male predominance of 59.10%. High blood pressure and diabetes are the two main causes. The start of dialysis on a temporary catheter represents 81.5% of cases, the initial management requires emergency dialysis in 91.2% of cases. In total, 97.1% of chronic hemodialysis patients use an arteriove-nous fistula as a permanent vascular access. Conclusion: Our study population is younger than that of developed countries and has fewer comorbidities and disabilities but lower survival and high mortality. The developing national chronic kidney disease stage V registry is becoming an absolute necessity. It will allow to have a better knowledge of its epidemiology and the needs of its care in each region. It can contribute to improving the prevention and management of this disease.


Introduction: La maladie rénale chronique stade V, par son incidence et sa prévalence qui ne cessent d'augmenter en Algérie et dans le monde, la morbi-mortalité qu'elle engendre et le coût élevé de sa prise en charge, représente un enjeu majeur de santé publique. Notre objectif est de décrire l'épidémiologie de cette maladie, traitée dans le Sud-Est algérien. Patients et méthodes: Dans notre étude régionale multicentrique, prospective à visée descriptive, tous les patients atteints de maladie rénale chronique stade V, résidant et traités dans le Sud-Est algérien entre le 1er septembre 2016 et le 31 décembre 2017, ont été inclus et suivis jusqu'au 31 décembre 2018. Résultats: La maladie rénale chronique stade V est une pathologie fréquente dans la région : 1 934 patients ont été inclus. Elle touche principalement les jeunes : l'âge moyen des patients était de 50,17 ± 16,98 ans, avec une prédominance masculine à 59,10 %. L'hypertension artérielle et le diabète représentent les deux principales causes. Les démarrages de dialyse sur cathéter temporaire représentent 81,5 % des cas, la prise en charge initiale nécessite la dialyse en urgence dans 91,2 % des cas. Un total de 97,1 % des patients hémodialysés chroniques utilisent une fistule artérioveineuse comme abord vasculaire permanent. Conclusion: Notre population d'étude est plus jeune que celle des pays développés et présente un nombre moins important de comorbidités et de handicaps, mais une survie inférieure et une mortalité élevée. Le développement du registre national de la maladie rénale chronique stade V devient une nécessité absolue. Il va permettre une meilleure connaissance de son épidémiologie et des besoins pour sa prise en charge dans chaque région. Il peut contribuer à l'amélioration de la prévention et de la prise en charge de cette maladie.


Asunto(s)
Fallo Renal Crónico , Humanos , Masculino , Adolescente , Adulto , Persona de Mediana Edad , Anciano , Femenino , Estudios Prospectivos , Argelia/epidemiología , Fallo Renal Crónico/epidemiología , Fallo Renal Crónico/terapia , Diálisis Renal/efectos adversos , Comorbilidad
6.
Nutrients ; 14(11)2022 May 29.
Artículo en Inglés | MEDLINE | ID: mdl-35684085

RESUMEN

The 25-hydroxyvitamin D3 (25OHD3) deficiency in chronic kidney disease (CKD) is associated with immune system dysfunction (pro-inflammatory cytokines storm) through macrophages renal infiltration, oxidative stress (OxS) damage and athero-thromboembolic risk. Conversely, cholecalciferol supplementation (25OHD-S) prevents kidney fibrosis by inhibition of vascular calcification and nephrotic apoptosis (nephrons reduction). The objective of this study was to investigate the pleiotropic effects of 25OHD-S on immunomodulation, antioxidant status and in protecting against thromboembolic events in deficiency CKD Black and White individuals living in the Southern Sahara (SS). The oral 25OHD-S was evaluated in 60,000 IU/month/36 weeks versus in 2000 IU/day/24 weeks in Black (n = 156) and White (n = 150). Total serum vitamin D was determined by liquid chromatography-tandem mass spectrometry. All biomarkers of pro-inflammatory cytokines (PIC) were assessed by ELISA tests. OxS markers were assessed by Randox kits. Homocysteine and lipoproteine (a) were evaluated by biochemical methods as biomarkers of atherothromboembolic risk. All statistical analyses were performed with Student's t-test and one-way ANOVA. The Pearson test was used to calculate the correlation coefficient. The means will be significantly different at a level of p value < 0.05. Multiple logistic regressions were performed using Epi-info and Statview software. Vitamin D deficiency alters the PIC profile, OxS damage and atherothrombogenic biomarkers in both SS groups in the same manner; however, these disorders are more acute in Black compared to White SS individuals. The results showed that the serum 25OHD3 concentrations became normal (>75 nmol/L or >30 ng/mL) in the two groups. We have shown that the dose and duration of 25OHD-S treatment are not similar in Black SS residents compared to White SS subjects, whilst the same inhabit the south Sahara environment. It appears that a high dose intermittent over a long period (D60: 36 weeks) was more efficient in Black people; while a lower dose for a short time is sufficient (D2: 24 weeks) in their White counterparts. The oral 25OHD-S attenuates PIC overproduction and OxS damage, but does not reduce athero-thromboembolic risk, particularly in Black SS residents.


Asunto(s)
Insuficiencia Renal Crónica , Deficiencia de Vitamina D , Colecalciferol , Síndrome de Liberación de Citoquinas , Citocinas , Suplementos Dietéticos , Humanos , Estrés Oxidativo , Insuficiencia Renal Crónica/complicaciones , Insuficiencia Renal Crónica/tratamiento farmacológico , Vitamina D , Deficiencia de Vitamina D/complicaciones , Deficiencia de Vitamina D/tratamiento farmacológico
7.
Ann Biol Clin (Paris) ; 76(3): 313-325, 2018 06 01.
Artículo en Francés | MEDLINE | ID: mdl-29661746

RESUMEN

The 1-25-hydroxyvitamine D (1-25OHD) or calcitriol deficiency in chronic kidney disease (CKD) patients was associated with increases vascular calcification risk, nephrons reduction, bone deficit and cardiovascular mortality by atherosclerosis. The objective of this study was to investigate the pleiotropic effects of 200.000 IU (D200 group) every 3 months versus 30.000 IU (D30 group) every month dose vitamin D supplementation in stage 3 CKD patients. A cohort of 132 adult subjects was randomized into 2 groups according to dose vitamin D supplementation in deficient subjects (25OHD <50 nmol/L or <20 ng/mL). Serum 25OHD levels were assessed before and after 6 and 12 months of vitamin D supplementation. Patients were phenotyped for IRS according to NCEP/ATPIII. Glomerular filtration rate (GFR) by the MDRD formula. Insulin resistance was evaluated by the Homa-IR model. IRS clusters by Cobas Integra 400®. PTH, Cortisol and IGF-1 were determined by radioimmunologic methods. The 25OHD profile was analyzed by LC-MS/MS. Results showed that vitamin D supplementation increased serum 25OHD concentrations (>75 nmol/L or >30 ng/mL) in both groups; however, the supplementation benefits are more significant in D30 group than in D200 group. We noted a highlighted improvement of kidney function, an inhibition of GFR collaps, a safe reduction of proteinuria, a significant PTH and C-reactive protein (inflammation) levels attenuation, concomitantly with cortisolemia normalization and decreased IGF-1 depletion. Nevertheless, homocysteine and Lp(a) concentrations remain increased, not modulated by vitamin D treatment. This study shows that continuous low doses (30.000 IU every month) are recommended for intermittent high doses (200.000 IU every 3 months) vitamin D supplementation. Our study suggests that the serum 25OHD profile can be considered a reliable biomarker in the bioclinic CKD status to stage stabilization and inhibit its evolution.


Asunto(s)
Colecalciferol/administración & dosificación , Enfermedades del Sistema Endocrino/complicaciones , Resistencia a la Insulina/fisiología , Síndrome Metabólico/complicaciones , Insuficiencia Renal Crónica/tratamiento farmacológico , Deficiencia de Vitamina D/tratamiento farmacológico , Administración Oral , Adulto , Colecalciferol/análisis , Suplementos Dietéticos , Progresión de la Enfermedad , Enfermedades del Sistema Endocrino/sangre , Enfermedades del Sistema Endocrino/tratamiento farmacológico , Femenino , Hormonas/análisis , Hormonas/sangre , Humanos , Masculino , Síndrome Metabólico/sangre , Síndrome Metabólico/tratamiento farmacológico , Insuficiencia Renal Crónica/sangre , Insuficiencia Renal Crónica/complicaciones , Vitamina D/análisis , Vitamina D/sangre , Deficiencia de Vitamina D/sangre , Deficiencia de Vitamina D/complicaciones
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