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1.
Article in English | MEDLINE | ID: mdl-29667173

ABSTRACT

BACKGROUND: Heart surgery requiring cardiopulmonary bypass (CPB) causes an inflammatory response which may further induce acute kidney injury (AKI). In the present randomized controlled study we evaluated whether corticosteroids can prevent CPB related AKI in neonates undergoing heart surgery. METHODS: Forty neonates were randomized to receive 2 mg/kg methylprednisolone followed by hydrocortisone infusion 0.2 mg/kg/h perioperatively with tapering doses for 5 days, or placebo administered in a similar fashion. The primary outcome was the inflammatory response (plasma concentrations of interleukins 6 and 10). The correspondence of the interleukin concentrations with AKI was analysed as secondary outcome. In addition, plasma and urine neutrophil gelatinase-associated lipocalin (NGAL), plasma cystatin C, and urine kidney injury molecule-1 (KIM-1) levels were measured. RESULTS: Six patients (15%) developed post-operative AKI. No significant difference in the AKI occurrence between the treatment (n = 2) and the placebo (n = 4) groups could be found (risk ratio 2.00, 95% confidence interval 0.41-9.71; P = .661) despite significant reduction in inflammatory response in the treatment group. One patient in the treatment group and two patients in the placebo group required acute peritoneal dialysis. Plasma creatinine and cystatin C or urine NGAL and KIM-1 concentrations did not differ between the treatment and the placebo group. CONCLUSIONS: Significantly reduced inflammatory reaction induced by corticosteroid treatment in neonates undergoing cardiac surgery did not reduce the incidence of AKI defined by KDIGO classification or decrease the rise of AKI biomarkers.

2.
Acta Paediatr ; 106(2): 322-326, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27759901

ABSTRACT

AIM: The human leucocyte antigen (HLA) allele and haplotype frequencies of the Finnish population are unique because of the restricted and homogenous gene population. There are no published data on HLA genotype associations in paediatric autoimmune liver diseases in Scandinavia. This study characterised the HLA genotypes of children with autoimmune liver or biliary disease in Finland. METHODS: The study cohort comprised 19 paediatric patients (13 female) aged three years to 15 years treated for autoimmune liver or biliary disease at the Children's Hospital, Helsinki University Hospital, between 2000 and 2011, and followed up for four years and three months to 14.6 years. We genotyped HLA-B and HLA-DRB1 in the children, and the HLA antigen frequencies were compared with 19 807 records from the Finnish Bone Marrow Donor Registry. RESULTS: All paediatric patients with autoimmune liver or biliary disease had either autoimmune HLA haplotype B*08;DRB1*03 or DRB1*13. These were significantly more common among patients with autoimmune hepatitis, primary sclerosing cholangitis and autoimmune hepatitis/primary sclerosing cholangitis overlap syndrome than the Finnish control population. HLA RB1*04 was not found in the study cohort. CONCLUSION: Our study found that B*08, DRB1*03 and DRB1*13 were significantly associated with autoimmune liver and biliary diseases in Finnish paediatric patients.


Subject(s)
Biliary Tract Diseases/genetics , HLA-B8 Antigen/genetics , HLA-DRB1 Chains/genetics , Hepatitis, Autoimmune/genetics , Adolescent , Child , Child, Preschool , Female , Finland , Humans , Male , White People/genetics
3.
Am J Transplant ; 14(12): 2887-92, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25359127

ABSTRACT

A 15-year-old boy with a posterior urethral valve received a deceased donor kidney transplant (KT) in March 2011. Basiliximab induction followed by tacrolimus-based triple medication was used as immunosuppression. Eleven months after KT, the graft function deteriorated and the biopsy demonstrated interstitial nephritis suggestive of acute rejection. BK polyomavirus (BKPyV) surveillance in urine and plasma was negative. The patient received methylprednisolone pulses and anti-thymocyte globulin. Immunohistochemistry was positive for simian virus 40 (SV40) large T-antigen (LTag) in the biopsies, and quantitative polymerase chain reaction for JC polyomavirus (JCPyV) indicated high viral loads in urine and borderline levels in plasma. Immunosuppression was reduced and follow-up biopsies showed tubular atrophy and interstitial fibrosis. Two years after KT, antibody-mediated rejection resulted in graft loss and return to hemodialysis. Retrospective serologic work-up indicated a primary JCPyV infection with seroconversion first for IgM, followed by IgG, but no indication of BKPyV infection. In the SV40 LTag positive biopsies, JCPyV deoxyribonucleic acid (DNA) with archetype noncoding control region was detected, while BKPyV DNA was undetectable. To the best of our knowledge, this is the first reported case of primary JCPyV infection as the cause of PyV-associated nephropathy in KT.


Subject(s)
Graft Rejection/etiology , Kidney Failure, Chronic/surgery , Kidney Transplantation , Nephritis, Interstitial/virology , Polyomavirus Infections/virology , Tumor Virus Infections/virology , Adolescent , DNA, Viral/genetics , Graft Rejection/diagnosis , Humans , Immunosuppressive Agents/therapeutic use , JC Virus/pathogenicity , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/virology , Male , Nephritis, Interstitial/diagnosis , Polyomavirus Infections/complications , Postoperative Complications , Prognosis , Renal Dialysis , Tumor Virus Infections/complications , Viral Load
4.
Am J Transplant ; 12(10): 2815-24, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22702386

ABSTRACT

Liver transplantation (LT) predisposes to metabolic derangements and increases the risk for cardiovascular disease. We conducted a national cross-sectional study of all pediatric recipients who underwent LT between 1987 and 2007. We measured serum levels of noncholesterol sterols (surrogate markers of cholesterol synthesis and intestinal absorption) and fibroblast growth factor 21 (FGF21) in 49 patients (74% of survivors) at a median of 10 years posttransplant and in 93 controls matched for age and gender. Although serum cholesterol levels were similar in patients and controls, patients displayed increased whole-body synthesis and decreased intestinal absorption of cholesterol compared with controls (lathosterol to cholesterol ratio 129 ± 55 vs. 96 ± 41, respectively, p < 0.001; campesterol to cholesterol ratio 233 ± 91 vs. 316 ± 107, respectively; p < 0.001). Azathioprine (r =-0.383, p = 0.007) and low-dose methylpredisolone (r =-0.492, p < 0.001) were negatively associated with lathosterol/sitosterol ratio reflecting a favorable effect on cholesterol metabolism. FGF21 levels were higher in patients than in controls (248 pg/mL vs. 77 pg/mL, p < 0.001). In healthy controls, FGF21 was associated with cholesterol metabolism, an association missing in LT recipients. Normal serum lipids are achievable in long-term survivors of pediatric LT, but changes in cholesterol metabolism and increased FGF21 levels may explicate later cardiovascular risk.


Subject(s)
Cholesterol/metabolism , Fibroblast Growth Factors/blood , Liver Transplantation , Adolescent , Adult , Child , Female , Humans , Male , Young Adult
5.
Am J Transplant ; 12(2): 420-7, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22050653

ABSTRACT

The long-term impact of pediatric liver transplantation (LT) and its complications on general health, health-related quality of life (HRQoL) and sexual health were assessed. We conducted a national cross-sectional study of all pediatric recipients who underwent LT between 1987 and 2007. Of 66 survivors, 57 participants (86%) were compared to randomly chosen healthy controls (n = 141) at 10.7 ± 6.6 years posttransplant. PedsQL4.0, SF-36, DISF-SR and AUDIT questionnaires for appropriate age groups were used. Patients and controls <7 years had similar HRQoL and 54% of patients aged over 7 scored within the controls' normal range on all HRQoL domains. In adult survivors, physical functioning and general health were decreased (p < 0.05). Biliary complications, reoperations and obesity were independently associated with reduced HRQoL (p < 0.05 for all). Still 64% of adult survivors considered their health excellent. Sexual health was similar to controls but LT recipients may experience problems with their orgasm strength (p = 0.050) and condom-based contraception was more common after LT than among controls (58% and 12%, p < 0.001). In conclusion, normal HRQoL and sexual health are achievable post-LT.


Subject(s)
Health Status , Liver Transplantation/psychology , Quality of Life , Registries , Sexual Behavior/physiology , Adolescent , Adult , Child , Cross-Sectional Studies , Female , Finland , Follow-Up Studies , Humans , Male , Retrospective Studies , Time Factors , Treatment Outcome , Young Adult
6.
Am J Transplant ; 8(1): 216-21, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17973958

ABSTRACT

A 12-month-old boy and his 16-year-old aunt became acutely ill 6 months apart and were diagnosed to have atypical hemolytic uremic syndrome (aHUS). Genetic analysis revealed heterozygous R1215Q mutation in complement factor H (CFH) in both patients. The same mutation was found in five healthy adult relatives indicating incomplete penetrance of the disease. The patients developed terminal renal failure and experienced reversible neurological symptoms in spite of plasma exchange (PE) therapy. In both cases, liver-kidney transplantation was successfully performed 6 months after the onset of the disease. To minimize complement activation and prevent thrombotic microangiopathy or overt thrombotic events due to the malfunctioning CFH, extensive PE with fresh frozen plasma was performed pre- and perioperatively and anticoagulation was started a few hours after the operation. No circulatory complications appeared and all four grafts started to function immediately. Also, no recurrence or other major clinical setbacks have appeared during the postoperative follow-up (15 and 9 months) and the grafts show excellent function. While more experience is needed, it seems that liver-kidney transplantation combined with pre- and perioperative PE is a rational option in the management of patients with aHUS caused by CFH mutation.


Subject(s)
Amino Acid Substitution/genetics , Complement Factor H/genetics , Hemolytic-Uremic Syndrome/genetics , Hemolytic-Uremic Syndrome/surgery , Kidney Transplantation , Liver Transplantation , Adolescent , Female , Genetic Carrier Screening , Hemolytic-Uremic Syndrome/therapy , Humans , Infant , Male , Pedigree , Plasma Exchange
7.
Am J Transplant ; 8(1): 150-7, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17973968

ABSTRACT

Long-term complications related to immunosuppressive medication are an important problem after liver transplantation (OLT). This study was carried out to evaluate the bone health and risk factors for osteoporosis and fractures in 40 pediatric liver transplant recipients. The results of 208 longitudinal bone mineral density (BMD) measurements were analyzed retrospectively. In addition, a dual-energy X-ray absorptiometry was performed to assess the bone mineral content more precisely and to detect subclinical vertebral fractures (VF). The median age of the patients was 14 years and mean postoperative follow-up 7.0 years. The results showed that over half (58%) had lumbar spine (LS) Z-score

Subject(s)
Liver Transplantation/adverse effects , Postoperative Complications/etiology , Postoperative Complications/physiopathology , Adolescent , Adult , Bone Density/physiology , Child , Child, Preschool , Cross-Sectional Studies , Female , Follow-Up Studies , Fractures, Bone/etiology , Fractures, Bone/metabolism , Fractures, Bone/physiopathology , Humans , Infant , Liver Transplantation/physiology , Longitudinal Studies , Male , Osteoporosis/etiology , Osteoporosis/metabolism , Osteoporosis/physiopathology , Postoperative Complications/metabolism , Risk Assessment
8.
Kidney Int ; 70(8): 1423-31, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16941028

ABSTRACT

Congenital nephrotic syndrome of the Finnish type (NPHS1) is a rare genetic disease caused by mutations in the NPHS1 gene encoding a major podocyte slit-diaphragm protein, nephrin. Patients with NPHS1 have severe nephrotic syndrome from birth and develop renal fibrosis in early childhood. In this work, we studied the development of glomerular sclerosis in kidneys removed from 4- to 44-month-old NPHS1 patients. The pathological lesions and expression of glomerular cell markers were studied in nephrectomized NPHS1 and control kidneys using light and electron microscopy and immunohistochemistry. An analysis of 1528 glomeruli from 20 patients revealed progressive mesangial sclerosis and capillary obliteration. Although few inflammatory cells were detected in the mesangial area, paraglomerular inflammation and fibrosis was common. The podocytes showed severe ultrastructural changes and hypertrophy with the upregulation of cyclins A and D1. Podocyte proliferation, however, was rare. Apoptosis was hardly detected and the expression of antiapoptotic B-cell lymphoma-2 and proapoptotic p53 were comparable to controls. Moderate amounts of podocytes were secreted into the urine of NPHS1 patients. Shrinkage of the glomerular tuft was common, whereas occlusion of tubular opening or protrusion of the glomerular tuft into subepithelial space or through the Bowman's capsule were not detected. The results indicate that, in NPHS1 kidneys, the damaged podocytes induce progressive mesangial expansion and capillary obliteration. Podocyte depletion, glomerular tuft adhesion, and misdirected filtration, however, seem to play a minor role in the nephron destruction.


Subject(s)
Kidney Glomerulus/pathology , Nephrotic Syndrome/congenital , Nephrotic Syndrome/pathology , Apoptosis , Cell Proliferation , Child, Preschool , Disease Progression , Epithelium/pathology , Glomerular Mesangium/blood supply , Glomerular Mesangium/pathology , Humans , Hypertrophy , Infant , Kidney Glomerulus/blood supply , Membrane Proteins/genetics , Mutation , Nephrotic Syndrome/genetics , Podocytes/pathology , Sclerosis
9.
Am J Transplant ; 6(2): 324-30, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16426316

ABSTRACT

The occurrence of scoliosis in children after solid organ transplantation is not known. A total of 196 children, which is 93% of patients surviving kidney, liver and heart transplantation in our country, participated in a cross-sectional survey. All children were screened for rib hump, and those with clinically significant hump (over 6 degrees ) underwent radiographs of the spine. The occurrence of scoliosis was compared to data obtained from a previously published comparison group. Forty-three (21.9%) of the patients had scoliosis greater than 10 degrees , and 21 (10.7%) of them had curves greater than 20 degrees . The RR (95% CI) for scoliosis needing treatment (over 20 degrees ) was 17.0 (6.75-42.7) in the patients as compared with control population. The occurrence of scoliosis was 17.9% of the kidney, 13.6% of the liver and 51.7% of the heart transplant patients (p < 0.001). In a logistic regression model, heart transplantation (OR (95% CI) 7.27 (2.62-20.2)) and growth hormone treatment (3.98 (1.77-8.94)) were most significant risk factors for scoliosis. The risk of scoliosis is increased in patients with solid organ transplantation. Pediatricians treating these patients should be aware of this increased risk to diagnose early curves and to refer these patients to an orthopedic surgeon.


Subject(s)
Bone Density , Heart Transplantation/adverse effects , Kidney Transplantation/adverse effects , Liver Transplantation/adverse effects , Scoliosis/epidemiology , Adolescent , Child , Child, Preschool , Cross-Sectional Studies , Female , Finland/epidemiology , Human Growth Hormone/therapeutic use , Humans , Infant , Male , Postoperative Complications/epidemiology
10.
Transplant Proc ; 37(2): 945-6, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15848583

ABSTRACT

We wanted to develop an immunostaining method of urine cytopreparations to detect polyoma virus infection by using fresh urine samples and staining with the monoclonal SV40 antibody and to compare the findings to the demonstration of decoy cells in the urine or to kidney histology. Routine urine samples from pediatric kidney transplant patients were collected either early after transplantation or later, cytocentrifuged, and immunostained with SV40-T-antibody. The number of SV40-T-antigen-positive epithelial cells was counted in the cytopreparations and compared to the findings in routine urine cytology and transplant histology. Immunostaining of urine cytology with SV40-T-ab demonstrated clearly that the infected epithelial cells and the rate of infection could be estimated by semiquantitative counting. There was strong correlation between the findings in the urine and in the biopsies, but in the urine preparations the number of infected cells was much higher than in the biopsies. The high number of SV40-positive cells in the urine also correlated to the severity of clinical infection and to the state of transplant. Immunostaining of urine cytology with SV40-T-antibody seems to be useful in the diagnosis and follow-up of polyoma virus reactivation disease in transplant patients, especially in children with renal transplants.


Subject(s)
Antigens, Polyomavirus Transforming/urine , Kidney Transplantation/adverse effects , Polyomavirus Infections/epidemiology , Simian virus 40/isolation & purification , Tumor Virus Infections/epidemiology , Biopsy , Humans , Immunohistochemistry/methods , Kidney/virology , Polyomavirus Infections/urine , Postoperative Complications/epidemiology , Postoperative Complications/virology , Tumor Virus Infections/urine
11.
J Med Genet ; 41(2): 92-8, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14757854

ABSTRACT

Mulibrey nanism (MUL) is an autosomal recessive disease caused by mutations in the TRIM37 gene encoding the peroxisomal TRIM37 protein of unknown function. In this work, we analysed the clinical characteristics of 85 Finnish patients with MUL, most of whom were homozygous for the Finn major mutation of TRIM37. The patients' hospital records from birth to the time of the diagnosis at age 0.02-52 years (median 2.1 years) were retrospectively analysed. All except four of the patients (95%) had a prenatal onset growth failure without postnatal catch up growth. The mean length standard deviation score (SDS) was -3.1 and -4.0 at birth and at diagnosis, respectively. In infancy, feeding difficulties, and respiratory tract infections were the most common problems. Congestive heart failure and pericardial constriction were diagnosed during infancy in 12% and 6% of the patients, respectively. At the time of the diagnosis, characteristic craniofacial features of scaphocephaly, facial triangularity, high and broad forehead, and low nasal bridge were evident in over 90% of the patients. In addition, practically all patients were gracile and had thin extremities. Other findings included a peculiar high-pitched voice (96%), yellowish dots in ocular fundi (79%), cutaneous naevi flammei (65%), hepatomegaly (45%), and fibrous dysplasia of long bones (25%). Mild muscular hypotonicity (68%) was the only neurological abnormality. The clinical features of the Finnish patients with MUL formed a distinct entity. The most consistent findings were growth failure and characteristic craniofacial features. However, organ manifestations varied considerably in early childhood. Based on these findings, we propose new diagnostic criteria for MUL.


Subject(s)
Dwarfism/diagnosis , Nuclear Proteins , Abnormalities, Multiple/blood , Abnormalities, Multiple/diagnostic imaging , Abnormalities, Multiple/genetics , Adolescent , Adult , Child , Child, Preschool , Craniofacial Abnormalities/blood , Craniofacial Abnormalities/diagnostic imaging , Craniofacial Abnormalities/genetics , Delivery, Obstetric , Dwarfism/blood , Dwarfism/diagnostic imaging , Dwarfism/genetics , Female , Humans , Infant , Infant, Newborn , Leg Bones/diagnostic imaging , Leg Bones/pathology , Male , Middle Aged , Mutation/genetics , Pregnancy , Proteins/genetics , Radiography , Retrospective Studies , Tripartite Motif Proteins , Ubiquitin-Protein Ligases
12.
Acta Paediatr ; 91(8): 915-9, 2002.
Article in English | MEDLINE | ID: mdl-12222715

ABSTRACT

AIM: To evaluate the relationship between absolute neutrophil count and C-reactive protein (CRP) in the recovery phase of neutropenic fever among paediatric patients with cancer. METHODS: A total of 102 paediatric oncology patients with 177 episodes of fever and neutropenia was studied prospectively in a two-centre setting. Antimicrobial therapy was discontinued 9 d (mean) post-initiation with a mean absolute neutrophil count of 1.8 x 10(9) l(-1) and CRP of 32 mg l(-1). RESULTS: The mean level of CRP below 20 mg l(-1) was reached on day 12. The level of CRP peaked on the day following the commencement of antimicrobial therapy. Throughout the episodes of fever and neutropenia higher levels of CRP were associated with a lower absolute neutrophil count. Following defervescence the pace of marrow recovery as evidenced by an increasing absolute neutrophil count to > 0.2 and > 0.5 x 10(9) l(-1) was more rapid than the normalization of serum CRP. There was a 2-3 d lag period between absolute neutrophil count exceeding the level of 200 x 10(6) l(-1) and the return of CRP to a baseline level. All episodes were treated successfully and there were no fatalities. CONCLUSION: Among patients recovering from neutropenia and fever the signs of marrow recovery remain the key criterion in evaluating the safety of discontinuing antimicrobial therapy, with serum CRP remaining more of an indicator of ongoing tissue repair.


Subject(s)
C-Reactive Protein/analysis , Fever/blood , Fever/immunology , Neoplasms/immunology , Neutropenia/blood , Neutropenia/immunology , Neutrophils/immunology , Regeneration/immunology , Wound Healing/immunology , Adolescent , Antineoplastic Agents/adverse effects , Child , Child, Preschool , Female , Fever/chemically induced , Humans , Infant , Leukocyte Count , Male , Neoplasms/drug therapy , Neutropenia/chemically induced , Predictive Value of Tests , Prospective Studies
13.
Ann Med ; 33(8): 526-33, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11730159

ABSTRACT

The sieving of plasma components occurs in the kidney through the glomerular capillary wall. This filter is composed of three layers: endothelium, glomerular basement membrane (GBM), and podocyte foot processes connected by slit diaphragms. Defects in this barrier lead to proteinuria and nephrotic syndrome. Previously, defective GBM was regarded to be responsible for proteinuria. However, recent work on genetic diseases has indicated that podocytes and the slit diaphragm are crucial in restricting protein leakage. Congenital nephrotic syndrome of the Finnish type (NPHS1) is caused by mutations in a novel NPHS1 gene, which encodes for a cell adhesion protein, nephrin. This protein is synthesized by podocytes, and seems to be a major component of the slit diaphragm. In severe NPHS1, lack of nephrin leads to missing slit diaphragm. The role of nephrin in acquired kidney diseases remains unknown. In addition to nephrin, other podocyte proteins (podocin, alpha-actinin-4, CD2AP, FAT) have recently been identified and associated with the development of proteinuria. It seems that the slit diaphragm and its interplay with the podocyte cytoskeleton is critical for the normal sieving process, and defects in one of these components easily lead to proteinuria.


Subject(s)
Kidney Glomerulus/pathology , Nephrotic Syndrome/genetics , Proteins , Proteins/genetics , Proteinuria/genetics , Glomerulosclerosis, Focal Segmental/genetics , Humans , Kidney Glomerulus/metabolism , Membrane Proteins/metabolism , Mutation , Nephrotic Syndrome/complications , Nephrotic Syndrome/congenital , Phosphoproteins/metabolism , Proteins/metabolism
14.
Transplantation ; 71(6): 736-43, 2001 Mar 27.
Article in English | MEDLINE | ID: mdl-11330534

ABSTRACT

UNLABELLED: analysis detected rejections often before clinical signs. Half of the patients had increased serum creatinine concentration and 38% had fever at the time of rejection diagnosis. Both signs were present in only 19% of the episodes. A decrease in urine output (>20%) was seen in a third of the episodes. The rejections responded well to oral methylprednisolone (3 mg/kg/day), and lymphoglobulins were needed in only 12% of the episodes. More than 90% of the rejections were completely reversible and no transplant was lost because of acute rejection. CONCLUSION: The results indicate that FNAB is a safe and sensitive method for the diagnosis and follow-up of acute cellular rejection in pediatric recipients of different ages.


Subject(s)
Kidney Transplantation/immunology , Kidney Transplantation/pathology , Adolescent , Age Factors , Biopsy, Needle/methods , Biopsy, Needle/standards , Body Temperature , Child , Child, Preschool , Creatinine/blood , Feasibility Studies , Female , Graft Rejection/diagnosis , Humans , Infant , Male , Retrospective Studies , Treatment Outcome , Urination/physiology
15.
Am J Pathol ; 157(6): 1905-16, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11106563

ABSTRACT

Nephrin is a cell adhesion protein located at the slit diaphragm area of glomerular podocytes. Mutations in nephrin-coding gene (NPHS1) cause congenital nephrotic syndrome (NPHS1). We studied the developmental expression of nephrin, ZO-1 and P-cadherin in normal fetal kidneys and in NPHS1 kidneys. We used in situ hybridization and immunohistochemistry at light and electron microscopic levels. Nephrin and zonula occludens-1 (ZO-1) were first expressed in late S-shaped bodies. During capillary loop stage, nephrin and ZO-1 localized at the basal margin and in the cell-cell adhesion sites between developing podocytes, especially in junctions with ladder-like structures. In mature glomeruli, nephrin and ZO-1 concentrated at the slit diaphragm area. P-cadherin was first detected in ureteric buds, tubules, and vesicle stage glomeruli. Later, P-cadherin was seen at the basal margin of developing podocytes. Fetal NPHS1 kidneys with Fin-major/Fin-major genotype did not express nephrin, whereas the expression of ZO-1 and P-cadherin was comparable to that of control kidneys. Although early junctional complexes proved structurally normal, junctions with ladder-like structures and slit diaphragms were completely missing. The results indicate that nephrin is dispensable for early development of podocyte junctional complexes. However, nephrin appears to be essential for formation of junctions with ladder-like structures and slit diaphragms.


Subject(s)
Fetus/physiology , Intercellular Junctions/physiology , Kidney/embryology , Proteins/physiology , Cadherins/metabolism , Embryonic and Fetal Development , Humans , Kidney Glomerulus/embryology , Membrane Proteins/metabolism , Microscopy, Immunoelectron , Mutation , Phosphoproteins/metabolism , Proteins/genetics , Reference Values , Zonula Occludens-1 Protein
16.
Pediatr Nephrol ; 14(10-11): 889-97, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10975294

ABSTRACT

Clinical outcome under adequacy control was studied in 10 pediatric patients under 5 years and 11 patients over 5 years of age on continuous peritoneal dialysis (PD). Outcome was compared between the age groups and with our previous results in patients under 5 years of age. Peritoneal equilibration test and 24-h dialysate collection were performed. Laboratory data, clinical status, and diet were recorded. PD prescription was adjusted for these parameters. The mean weekly urea Kt/V was similar and stable in the two age groups (3.1+/-0.6 vs. 3.2+/-0.4 at baseline). The mean weekly creatinine clearance (C(Cr)) was at baseline significantly lower in the younger age group (58.7+/-11.9 vs. 78.0+/-14.9 l/week per 1.73 m2, P=0.004), but later similar. Urea Kt/V and C(Cr) correlated significantly. Hematological and biochemical parameters were stable, and catch-up growth was observed in 62% of the patients during 9 months of follow-up. The outcome for children under and over 5 years of age did not differ significantly. The clinical outcome in patients under 5 years of age improved under adequacy control, when compared with our previous results in patients of the same age. This suggests a positive effect of adequacy control on clinical outcome.


Subject(s)
Kidney Failure, Chronic/therapy , Peritoneal Dialysis , Adolescent , Antihypertensive Agents/therapeutic use , Catheterization/adverse effects , Child , Child Nutritional Physiological Phenomena , Child, Preschool , Growth , Humans , Hypertension/drug therapy , Hypertension/etiology , Infant , Infections/etiology , Kidney Failure, Chronic/blood , Kidney Failure, Chronic/metabolism , Kidney Failure, Chronic/physiopathology , Peritoneal Dialysis/adverse effects , Peritoneal Dialysis/instrumentation , Peritonitis/etiology , Treatment Outcome
17.
Kidney Int ; 58(3): 972-80, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10972661

ABSTRACT

BACKGROUND: Congenital nephrotic syndrome (NPHS1) is a rare disease inherited as an autosomally recessive trait. The NPHS1 gene mutated in NPHS1 children has recently been identified. The gene codes for nephrin, a cell-surface protein of podocytes. Two mutations, named Fin-major and Fin-minor, have been found in over 90% of the Finnish patients. In this study, we correlated the NPHS1 gene mutations to the clinical features and renal findings in 46 Finnish NPHS1 children. METHODS: Clinical data were collected from patient files, and kidney histology and electron microscopy samples were re-evaluated. The expression of nephrin was studied using immunohistochemistry, Western blotting, and in situ hybridization. RESULTS: Nephrotic syndrome was detected in most patients within days after birth regardless of the genotype detected. No difference could be found in neonatal, renal, cardiac, or neurological features in patients with different mutations. Nephrin was not expressed in kidneys with Fin-major or Fin-minor mutations, while another slit diaphragm-associated protein, ZO-1, stained normally. In electron microscopy, podocyte fusion and podocyte filtration slits of various sizes were detected. The slit diaphragms, however, were missing. In contrast to this, a nephrotic infant with Fin-major/R743C genotype expressed nephrin in kidney had normal slit diaphragms and responded to therapy with an angiotensin-converting enzyme inhibitor and indomethacin. CONCLUSIONS: The most common NPHS1 gene mutations, Fin-major and Fin-minor, both lead to an absence of nephrin and podocyte slit diaphragms, as well as a clinically severe form of NPHS1, the Finnish type of congenital nephrotic syndrome.


Subject(s)
Mutation, Missense , Nephrotic Syndrome/genetics , Proteins/genetics , Blotting, Western , Finland , Gene Expression , Genes, Recessive , Genotype , Humans , Hypoproteinemia/congenital , Hypoproteinemia/genetics , In Situ Hybridization , Infant, Newborn , Kidney/chemistry , Kidney/ultrastructure , Membrane Proteins/analysis , Membrane Proteins/genetics , Microscopy, Electron , Nephrotic Syndrome/congenital , Phosphoproteins/analysis , Phosphoproteins/genetics , Proteins/analysis , Proteinuria/congenital , Proteinuria/genetics , RNA, Messenger/analysis , Zonula Occludens-1 Protein
18.
Transplantation ; 70(3): 480-7, 2000 Aug 15.
Article in English | MEDLINE | ID: mdl-10949191

ABSTRACT

BACKGROUND: We report a long-term prospective follow-up of renal allograft histology in children <5 years of age at transplantation (Tx). METHODS: Fifty-one kidney allograft recipients were prospectively followed for renal allograft histology and function up to 7 years after Tx. Twenty patients were recipients of kidneys from living related donors, and 31 were cadaveric kidney recipients. All patients received triple immunosuppression. Biopsies were analyzed according to the Banff classification and scored semiquantitatively. The "chronic allograft damage index" (CADI) was calculated. RESULTS: Five of seven grafts were lost because of nephrosis in patients with congenital nephrotic syndrome of the Finnish type. Most of the biopsies (52-69%) were considered normal (Banff classification), and the proportion with chronic allograft nephropathy did not increase with time. The median CADI score was 2.5 (scale: 0-36) at 1.5 years and 3.5 at 7 years. Recipients with an acute rejection episode had higher CADI scores than recipients without acute rejection episode. Patients with a high CADI score at 3 years had inferior graft function at 5 years. Recipients <2 years of age had CADI scores and numbers of acute rejection episode similar to recipients between 2 and 5 years of age. However, in contrast to the older recipients, the younger recipients did not improve their absolute glomerular filtration rate with time. CONCLUSIONS: The long-term histopathological findings were mostly mild and stable with time. Acute rejection episode had an impact on these changes and CADI predicted later graft function. Nonimmunological risk factors seem to be more important in the youngest recipients.


Subject(s)
Kidney Transplantation/pathology , Acute Disease , Age Factors , Child , Child, Preschool , Female , Follow-Up Studies , Graft Rejection , Graft Survival , Humans , Infant , Kidney Transplantation/adverse effects , Kidney Transplantation/physiology , Male , Prospective Studies , Risk Factors
19.
Transplantation ; 69(8): 1617-23, 2000 Apr 27.
Article in English | MEDLINE | ID: mdl-10836371

ABSTRACT

BACKGROUND: Infectious complications are a major cause of morbidity and mortality after organ transplantation. There are several reports on infections during the first months after transplantation, but there are very few data regarding infections in long-term survivors of pediatric organ transplantation. METHODS: The incidence and type of infections were retrospectively analyzed in 56 children who underwent 59 liver or renal transplantations. Follow-up was begun when the patient was sent home after a successful operation. All of the children received triple immunosuppression. RESULTS: During a mean follow-up of 4.8 years (total, 286 patient years), 1540 episodes of infection were recorded. The median incidence was 4.8 episodes/patient year. The greatest number was seen in the smallest children, 3 to 6 months after transplantation. Viral upper respiratory tract infections were the most common problem, accounting for half of the episodes (2.7 episodes/patient year). Gastroenteritis was the second most common viral infection. Only 45 episodes of infection with herpesviruses were recorded, and seven of those were caused by cytomegalovirus. Otitis media and sinusitis were the most common bacterial infections and complicated upper respiratory infection in 23% of episodes. Thirty-nine episodes of urinary tract infections were diagnosed, thirty-one in children with renal transplants. Other bacterial infections were rare, and only three episodes of verified bacterial sepsis were diagnosed. CONCLUSION: The frequency and type of infections in children with liver and renal transplants who are on triple immunosuppression are quite similar to those in age-matched healthy children.


Subject(s)
Infections/epidemiology , Kidney Transplantation , Liver Transplantation , Postoperative Complications/epidemiology , Adolescent , Bacterial Infections/epidemiology , Child , Child, Preschool , Female , Gastroenteritis/epidemiology , Herpesviridae Infections/epidemiology , Hospitalization , Humans , Incidence , Infant , Male , Reference Values , Respiratory Tract Infections/epidemiology , Retrospective Studies
20.
Proc Natl Acad Sci U S A ; 96(14): 7962-7, 1999 Jul 06.
Article in English | MEDLINE | ID: mdl-10393930

ABSTRACT

We describe here the size and location of nephrin, the first protein to be identified at the glomerular podocyte slit diaphragm. In Western blots, nephrin antibodies generated against the two terminal extracellular Ig domains of recombinant human nephrin recognized a 180-kDa protein in lysates of human glomeruli and a 150-kDa protein in transfected COS-7 cell lysates. In immunofluorescence, antibodies to this transmembrane protein revealed reactivity in the glomerular basement membrane region, whereas the podocyte cell bodies remained negative. In immunogold-stained thin sections, nephrin label was found at the slit between podocyte foot processes. The congenital nephrotic syndrome of the Finnish type (NPHS1), a disease in which the nephrin gene is mutated, is characterized by massive proteinuria already in utero and lack of slit diaphragm and foot processes. These features, together with the now demonstrated localization of nephrin to the slit diaphragm area, suggests an essential role for this protein in the normal glomerular filtration barrier. A zipper-like model for nephrin assembly in the slit diaphragm is discussed, based on the present and previous data.


Subject(s)
Epithelial Cells/physiology , Epithelial Cells/ultrastructure , Kidney Glomerulus/physiology , Kidney Glomerulus/ultrastructure , Proteins/analysis , Proteins/genetics , Cell Membrane/physiology , Cell Membrane/ultrastructure , Cloning, Molecular , Finland , Glomerular Filtration Rate , Humans , Membrane Proteins , Microscopy, Immunoelectron , Molecular Sequence Data , Mutation , Nephrotic Syndrome/genetics , Polymerase Chain Reaction , Recombinant Proteins/analysis
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