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Dive into the research topics where Àngel Argilés is active.

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Featured researches published by Àngel Argilés.


Blood Purification | 2002

Blood Pressure Is Correlated with Vitamin D3 Serum Levels in Dialysis Patients

Àngel Argilés; Ronan Lorho; Marie-Françoise Servel; Isabelle Couret; Guillaume Chong; Georges Mourad

Background/Aim: The blood pressure, the most influencing factor in cardiovascular disease in end-stage renal failure patients, follows a seasonal variation during the year. Since vitamin D3 is known to be related to sun exposure, we wanted to evaluate the putative participation of the vitamin D3 metabolism in blood pressure modifications. Methods: We studied 22 stable hemodialysis patients (11 females and 11 males, mean age ± SD 56 ± 1 year) who had been continuously treated in our dialysis unit for more than 1 year between 1994 and 1997 and did not receive pulse vitamin D3 treatment. Supine systolic and diastolic blood pressures were measured before every dialysis session (>12,000 measurements) and the intact parathormone (iPTH), 25-hydroxyvitamin D3 [25(OH)D3], and 1,25-dihydroxyvitamin D3 [1,25(OH)2D3] levels every 3 months (>300 determinations). The mean values of blood pressure per season and per patient were taken for analysis using a 4-year longitudinal study design. Results: The blood pressure varied during the years studied following a seasonal trend. It was highest during autumn and tended to decrease during spring and warmer months. Systolic as well as diastolic blood pressures were significantly correlated with the 25(OH)D3 levels (p = 0.0291 and p = 0.0327, respectively). No correlation was observed between blood pressure and 1,25(OH)2D3 or iPTH levels. Conclusions: There is a link between blood pressure and 25(OH)D3 level. This interrelation is not secondary to a iPTH modulation. Although it cannot be excluded that vitamin D3 and blood pressure vary following a third factor with seasonal variations, since vitamin D3 varies during the year, mainly following sun exposure, we suggest that vitamin D3 is one of the factors participating in the seasonal variation of the blood pressure. Other factors known to control the blood pressure and particularly the extracellular volume overload may also participate.


Cornea | 2002

Clinical, histopathologic, and ultrastructural characteristics of BIGH3 (TGFBI) amyloid corneal dystrophies are supportive of the existence of a new type of LCD: The LCDI

Clair-Florent Schmitt-Bernard; Christelle Schneider; Àngel Argilés

Purpose. To assess the morphologic differences of three types of lattice corneal dystrophies (LCDs) from histologic, immunohistochemical, and ultrastructural studies. Methods. Corneas from three patients, one LCD1, one His626Arg-LCD, and one LCD3A were processed for Congo red, &bgr;ig-h3541–564 antibodies immunostaining, and electron transmission microscopy studies. Control tissues were submitted to identical analyses and consisted of one cornea from a patient not having LCD and one skin biopsy from the patient suffering from LCD1. Results. The three corneas displayed birefringent congophilic deposits under polarized light, confirming their amyloid nature. The deposits differed regarding their shape and location in each of the corneas. A strong immunoreactivity for &bgr;ig-h3 was shown in the LCD1 and His626Arg-LCD deposits, which was faint for the LCD3A deposits. Ultrastructural analysis confirmed the dissimilarity of the deposits among the different types of LCD. No amyloid deposits were observed in the skin from the LCD1 patient, whereas immunostaining showed the presence of high amounts of &bgr;ig-h3. Conclusion. Our results show that &bgr;ig-h3 is involved in amyloid deposition in all the LCDs included in the study (LCD1, His626Arg-LCD, and LCD3A). These three forms of LCD, clinically different, were also distinguishable histologically, confirming that they belong to distinctive groups of LCDs. The absence of amyloid deposition in skin from the LCD1 patient supports cornea-specific amyloid formation. In light of the present clinical, histologic, and ultrastructural data, His626Arg and related LCDs constitute a separate group of LCD that could be considered as of intermediate type on clinical grounds.


Blood Purification | 1999

Analysis of the Influence of the Infusion Site on Dialyser Clearances Measured in an in vitro System Mimicking Haemodialysis and Haemodiafiltration

A. Ficheux; Àngel Argilés; J.Y. Bosc; C. Mion

Background: Blood flow (QB), dialysate flow (QD), and dialyser characteristics are the three major factors driving dialysis efficacy. Haemodiafiltration has added an increased convective volume to increase efficacy. We aimed to assess the influence of the infusion site of the replacement fluid in an in vitro system emulating haemodiafiltration. Methods: An in vitro system allowing us to control the dialysate temperature, concentration gradient, the flow of both dialyser sides over a range wider than that compatible with clinic, was set to evaluate the influence of the different parameters on dialysis efficacy. The total ion clearance was used as an accepted method for small molecule clearance assessment. Cellulose triacetate (CT190C, Baxter; FB170U, Nipro) and polysulfone (HF80, Fresenius) dialysers were included in the study. Dialysis as well as on-line diafiltration both with pre- and postdilutional infusion were assessed. The experimental conditions presented in this study included QD 620 and 970 ml/min. The convective flows ranged from 50 to 200 ml/min. Results: For a QD = 620 ml/min and a QB = 350 ml/min the total ion clearance ranged from 269 to 274 for HF80, from 291 to 294 for FB170 and from 294 to 302 for CT190. The variability of the measurements was very low (SD < 1%). Total ion clearance increased by 17–21% when QB was raised from 300 to 400 ml/min. Increasing QD from 420 to 970 ml/min (for QB = 350 ml/min), resulted in an increase in total ion clearance which was more marked at lower QD (from 420 to 620 ml/min) and plateaued thereafter (from 620 to 970 ml/min). Postdilutional on-line diafiltration with 100 ml/min of infusate resulted in an additional increase in total ion clearance of 5.4–8.6%. This increase was proportional to the infused volume. On the contrary, predilutional on-line diafiltration resulted in a decrease in total ion clearance which was also proportional to the infused volume (between –5.1 and –6.9% at 100 ml/min infusion volume and –9.7 to –12.9% at 200 ml/min). Conclusions: The present in vitro system provided accurate and reproducible results on dialyser clearances. Our experiments confirmed previous studies on the influence of QB and QD on dialyser efficacy. Further, they show that the proportional increase in postdilutional on-line diafiltration is lesser than that previously reported. More importantly, they also show that pre-dilution infusion in high efficiency systems results in a drop in dialyser clearance compared to dialysis alone, again proportional to the infusion rate. Thus, increasing the convective flow may increase dialysis efficacy even more than increasing QD alone. However, the choice of infusion site is crucial to obtaining this benefit in small molecule clearances.


Investigative Ophthalmology & Visual Science | 2000

BIGH3 exon 14 mutations lead to intermediate type I/IIIa of lattice corneal dystrophies

Clair-Florent Schmitt-Bernard; Guittard C; Arnaud B; Jacques Demaille; Àngel Argilés; Mireille Claustres; Tuffery-Giraud S


FEBS Journal | 2002

BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro Implications in the BIGH3-linked corneal dystrophies

Clair-Florent Schmitt-Bernard; Alain Chavanieu; Gudrun Herrada; Guy Subra; Bernard Arnaud; Jacques Demaille; Bernard Calas; Àngel Argilés


Biochemical and Biophysical Research Communications | 2000

In Vitro Creation of Amyloid Fibrils from Native and Arg124Cys Mutated βIGH3(110–131) Peptides, and Its Relevance for Lattice Corneal Amyloid Dystrophy Type I

Clair-Florent Schmitt-Bernard; Alain Chavanieu; Jean Derancourt; Bernard Arnaud; Jacques Demaille; Bernard Calas; Àngel Argilés


Clinical Science | 2000

α2-Macroglobulin, the main serum antiprotease, binds β2-microglobulin, the light chain of the class I major histocompatibility complex, which is involved in human disease

Annie Gouin-Charnet; Daniel Laune; Claude Granier; Jean-Claude Mani; Bernard Pau; Georges Mourad; Àngel Argilés


Kidney International | 2000

Influence of convection on small molecule clearances in online hemodiafiltration Technical Note

Alain Ficheux; Àngel Argilés; Henri Mion; Charles M. Mion


Biochemical and Biophysical Research Communications | 1997

α2-Macroglobulin Protects Some of the Protein Constituents of Dialysis-Associated Amyloidosis from Protease Degradation

Annie Gouin-Charnet; G. Mourad; Àngel Argilés


The Lancet | 1993

High-dose alfacalcidol for anaemia in dialysis

Àngel Argilés; Ronan Lorho; Georges Mourad; CharlesM. Mion

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Clair-Florent Schmitt-Bernard

Centre national de la recherche scientifique

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Georges Mourad

University of Montpellier

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Annie Gouin-Charnet

Centre national de la recherche scientifique

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Jacques Demaille

Centre national de la recherche scientifique

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Bernard Arnaud

Centre national de la recherche scientifique

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Ronan Lorho

Centre national de la recherche scientifique

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Alain Chavanieu

University of Montpellier

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Bernard Calas

University of Montpellier

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Alain Ficheux

Centre national de la recherche scientifique

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Charles M. Mion

Centre national de la recherche scientifique

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