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1.
Article Dans Anglais | WPRIM | ID: wpr-758975

Résumé

BACKGROUND: Cardiovascular disease and chronic kidney disease share several common risk factors. The Framingham risk score is hypothesized to predict chronic kidney disease development. We determined if the Framingham risk scoring system can correctly predict incident chronic kidney disease in the general population. METHODS: This study included 9,080 subjects who participated in the Korean Genome and Epidemiology Study between 2001 and 2014 and had normal renal function. The subjects were classified into low- ( 20%) risk groups based on baseline Framingham risk scores. The primary endpoint was de novo chronic kidney disease development (estimated glomerular filtration rate [eGFR], < 60 mL/min/1.73 m²). RESULTS: During a mean follow-up duration of 8.9 ± 4.3 years, 312 (5.3%), 217 (10.8%), and 205 (16.9%) subjects developed chronic kidney disease in the low, intermediate, and high risk groups, respectively (P < 0.001). Multivariable analysis after adjustment for confounding factors showed the hazard ratios for the high- and intermediate risk groups were 2.674 (95% confidence interval [CI], 2.197–3.255) and 1.734 (95% CI, 1.447–2.078), respectively. This association was consistently observed irrespective of proteinuria, age, sex, obesity, or hypertension. The predictive power of this scoring system was lower than that of renal parameters, such as eGFR and proteinuria, but increased when both were included in the prediction model. CONCLUSION: The Framingham risk score predicted incident chronic kidney disease and enhanced risk stratification in conjunction with traditional renal parameters in the general population with normal renal function.


Sujets)
Maladies cardiovasculaires , Études de cohortes , Épidémiologie , Études de suivi , Génome , Débit de filtration glomérulaire , Hypertension artérielle , Obésité , Études prospectives , Protéinurie , Insuffisance rénale chronique , Facteurs de risque
2.
Yonsei Medical Journal ; : 141-148, 2014.
Article Dans Anglais | WPRIM | ID: wpr-86929

Résumé

PURPOSE: The effect of different peritoneal dialysis (PD) modalities on the decline in residual renal function (RRF) is unclear due to inconsistencies among studies. In particular, the effect of automated peritoneal dialysis (APD) modalities [continuous cyclic peritoneal dialysis (CCPD) and nightly intermittent peritoneal dialysis (NIPD)] on RRF has not been examined in a large cohort. MATERIALS AND METHODS: We conducted a single-center retrospective study to investigate the association between PD modalities and decline in RRF in 142 incident PD patients [34 on CCPD, 36 on NIPD, and 72 on continuous ambulatory peritoneal dialysis (CAPD)]. RRF was measured within 2 months from PD start and at 1 year after PD initiation. RESULTS: The RRF at 1 year after PD initiation was 1.98+/-2.20 mL/min/1.73 m2 in CCPD patients and 3.63+/-3.67 mL/min/1.73 m2 in NIPD patients, which were moderately lower than 4.23+/-3.51 mL/min/1.73 m2 in CAPD patients (p=0.064). Moreover, there was no significant difference in the 1-year rate of decline of RRF between CCPD and NIPD patients, although APD patients had a faster 1-year RRF decline rate than CAPD patients (CCPD and NIPD vs. CAPD: -45.68 and -36.69 vs. 1.17%/year, p=0.045). APD was associated with a more rapid decline in RRF in patients with end-stage renal disease undergoing PD, although multivariate analysis attenuated the significance of this finding (beta=-31.50; 95% CI, -63.61 to 0.62; p=0.052). CONCLUSION: Our results suggest that CAPD might be more helpful than APD for preserving RRF during the first year of dialysis therapy, although there was no significant difference in the 1-year rate of decline of RRF between the two APD modalities.


Sujets)
Adulte , Femelle , Humains , Mâle , Adulte d'âge moyen , Débit de filtration glomérulaire/physiologie , Rein/anatomopathologie , Défaillance rénale chronique/thérapie , Dialyse péritonéale/effets indésirables , Études rétrospectives
3.
The Ewha Medical Journal ; : 139-143, 2013.
Article Dans Anglais | WPRIM | ID: wpr-71796

Résumé

Nephrotic syndrome is most commonly observed in membranous lupus nephritis in patients with systemic lupus erythematosus (SLE). However, other forms of idiopathic nephrotic syndrome rarely occur in these patients. Here, we report a case of SLE complicated by minimal change disease (MCD). A 24-year-old woman with SLE visited our hospital for generalized edema and heavy proteinuria. Laboratory tests did not support immunological exacerbation of lupus, while renal biopsy revealed diffusely effaced foot processes without electron-dense deposits that were consistent with MCD. Administration of high-dose corticosteroids and 6 subsequent cycles of monthly intravenous cyclophosphamide resulted in complete remission. Although nephrotic-range proteinuria recurred 1 month after switching to maintenance therapy with mycophenolate mofetil, complete remission was reestablished after a 6-month treatment with corticosteroids and cyclosporine. Physicians should be cautious in assessment and management of such a rare renal manifestation.


Sujets)
Femelle , Humains , Jeune adulte , Hormones corticosurrénaliennes , Biopsie , Cyclophosphamide , Ciclosporine , Oedème , Lupus érythémateux disséminé , Glomérulonéphrite lupique , Acide mycophénolique , Néphrose lipoïdique , Syndrome néphrotique , Protéinurie
4.
The Ewha Medical Journal ; : S25-S29, 2013.
Article Dans Anglais | WPRIM | ID: wpr-141198

Résumé

Primary amyloidosis has unfavorable prognosis, particularly with organ involvement. Here, we report a case of clinical remission of renal amyloidosis after autologous hematopoietic cell transplantation. A 51-year-old female patient visited our hospital due to generalized edema. Initial evaluation showed hyperlipidemia, hypoalbuminemia, and heavy proteinuria, which were consistent with nephrotic syndrome. However, IgM lamda type monoclonal gammopathy was detected in serum and urine electrophoresis studies. Renal biopsy showed Congo red-positive amyloid deposition in mesangial area, glomerular capillary walls, and arterioles and amyloid fibers were confirmed by electron microscopy. Immunohistochemial study of the biopsy tissue demonstrated systemic light-chain amyloidosis (AL amyloidosis). Multiple myeloma was not evident on bone marrow examination. She received autologous hematopoietic cell transplantation after high dose melphalan treatment. Complete remissions were achieved after the treatment, respectively. Our findings suggest the potential role of autologous peripheral blood stem cell transplantation in treatment of AL amyloidosis.


Sujets)
Femelle , Humains , Adulte d'âge moyen , Amyloïde , Amyloïdose , Artérioles , Biopsie , Myélogramme , Vaisseaux capillaires , Transplantation cellulaire , Congo , Oedème , Électrophorèse , Hyperlipidémies , Hypoalbuminémie , Immunoglobuline M , Melphalan , Microscopie électronique , Myélome multiple , Syndrome néphrotique , Paraprotéinémies , Transplantation de cellules souches de sang périphérique , Plaque amyloïde , Pronostic , Protéinurie , Transplants
5.
The Ewha Medical Journal ; : S25-S29, 2013.
Article Dans Anglais | WPRIM | ID: wpr-141199

Résumé

Primary amyloidosis has unfavorable prognosis, particularly with organ involvement. Here, we report a case of clinical remission of renal amyloidosis after autologous hematopoietic cell transplantation. A 51-year-old female patient visited our hospital due to generalized edema. Initial evaluation showed hyperlipidemia, hypoalbuminemia, and heavy proteinuria, which were consistent with nephrotic syndrome. However, IgM lamda type monoclonal gammopathy was detected in serum and urine electrophoresis studies. Renal biopsy showed Congo red-positive amyloid deposition in mesangial area, glomerular capillary walls, and arterioles and amyloid fibers were confirmed by electron microscopy. Immunohistochemial study of the biopsy tissue demonstrated systemic light-chain amyloidosis (AL amyloidosis). Multiple myeloma was not evident on bone marrow examination. She received autologous hematopoietic cell transplantation after high dose melphalan treatment. Complete remissions were achieved after the treatment, respectively. Our findings suggest the potential role of autologous peripheral blood stem cell transplantation in treatment of AL amyloidosis.


Sujets)
Femelle , Humains , Adulte d'âge moyen , Amyloïde , Amyloïdose , Artérioles , Biopsie , Myélogramme , Vaisseaux capillaires , Transplantation cellulaire , Congo , Oedème , Électrophorèse , Hyperlipidémies , Hypoalbuminémie , Immunoglobuline M , Melphalan , Microscopie électronique , Myélome multiple , Syndrome néphrotique , Paraprotéinémies , Transplantation de cellules souches de sang périphérique , Plaque amyloïde , Pronostic , Protéinurie , Transplants
6.
Article Dans Coréen | WPRIM | ID: wpr-652377

Résumé

PURPOSE: To review the results of resections of heterotopic ossification around the hip in patients with central nervous system injuries. MATERIALS AND METHODS: Heterotopic ossification was resected in ten hips of eight patients and followed for at least one year. Average age was 38.1 years (range, 21-56 years). We reviewed the charts and the radiographs for overall patient function, location of the lesion, radiographic evidence of maturation and any recurrence. Heterotopic ossification was resected regardless of the result of bone scan. RESULTS: All patients showed improved function. Three minimal recurrences and one moderate recurrence were identified at the last follow-up radiography, but the range of motion had not decreased due to recurrence. CONCLUSION: Severe heterotopic ossification around the hip in patients with spastic paralysis was resected, and it was found that the range of motion was improved in all patients and that the chance of recurrence was minimal, even though the bone scan showed hot uptake on the bone scan.


Sujets)
Adulte , Humains , Système nerveux central , Études de suivi , Articulation de la hanche , Hanche , Spasticité musculaire , Ossification hétérotopique , Paralysie , Radiographie , Amplitude articulaire , Récidive
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