Database : MEDLINE
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[PMID]: 24866598
[Au] Autor:Mira Moreno A; Montoya Lirola MD; García Tabar PJ; Galiano Baena JF; Tenza Tenza JA; Lobato Encinas JJ
[Ad] Address:Department of Urology, General Hospital University of Alicante, Alicante, Spain. Electronic address: ale_mimo@hotmail.com....
[Ti] Title:Incidence of infectious complications after extracorporeal shock wave lithotripsy in patients without associated risk factors.
[So] Source:J Urol;192(5):1446-9, 2014 Nov.
[Is] ISSN:1527-3792
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:PURPOSE: We determined the incidence of infectious complications (asymptomatic bacteriuria, urinary tract infection and urosepsis) in patients without associated risk factors treated with extracorporeal shock wave lithotripsy. MATERIALS AND METHODS: We performed an observational, prospective cohort study between October 2010 and June 2013. We included all patients without risk factors who were treated with extracorporeal shock wave lithotripsy for kidney or ureteral lithiasis. All patients underwent urine culture 5 days before the procedure. Another urine culture was performed 7 days after lithotripsy. No patient received antibiotics. RESULTS: Initially 366 patients with a mean ± SD age of 53 ± 13 years were enrolled in the study. A total of 64 patients (17.5%) underwent extracorporeal shock wave lithotripsy with a previously placed Double-J® stent. After lithotripsy urine culture was positive in 20 patients (5.8%), of whom 4 (1.2%) presented with symptomatic urinary infection and the remaining 4.6% showed no symptoms. Urosepsis did not develop in any case. In our study patient age was an independent risk factor for bacteriuria after lithotripsy. CONCLUSIONS: The incidence of infectious complications after extracorporeal shock wave lithotripsy in patients without risk factors is low. This leads us to conclude that without defined risk factors antibiotic prophylaxis is not justified. Also, elderly patients were more at risk for bacteriuria after extracorporeal shock wave lithotripsy and, thus, for a possible infectious complication.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1410
[Js] Journal subset:AIM; IM
[St] Status:In-Data-Review

  2 / 5730 MEDLINE  
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[PMID]: 25322624
[Au] Autor:Ernandez T; Bonny O
[Ti] Title:La lithiase rénale: un marqueur du risque cardiovasculaire. [Kidney stone as a cardiovascular risk marker].
[So] Source:Rev Med Suisse;10(441):1656-60, 2014 Sep 10.
[Is] ISSN:1660-9379
[Cp] Country of publication:Switzerland
[La] Language:fre
[Ab] Abstract:Most of the time, kidney stones are considered as minor, but painful events. However, several studies have recently shown an association between kidney stone and an increased cardio-vascular risk. We review here these studies and explore the underlying pathophysiological hypotheses. At the end, we propose that lithiasis should be considered as a red flag intervening early during life-time and allowing a check of cardiovascular risk factors and early preventive intervention. Such approach may be successful in reducing the incidence of cardio-vascular events in stone formers.
[Pt] Publication type:ENGLISH ABSTRACT; JOURNAL ARTICLE
[Em] Entry month:1410
[Js] Journal subset:IM
[St] Status:In-Process

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[PMID]: 23103120
[Au] Autor:Jorquera-Barquero E; Súarez-Marrero MC; Fernández Girón F; Borrero Martín JJ
[Ad] Address:Servicio de Dermatología Médico-Quirúrgica y Venereología, Hospital Juan Ramón Jiménez, Huelva, España. Electronic address: jorroc@aedv.es.
[Ti] Title:Oxalosis and livedo reticularis.
[So] Source:Actas Dermosifiliogr;104(9):815-8, 2013 Nov.
[Is] ISSN:1578-2190
[Cp] Country of publication:Spain
[La] Language:eng; spa
[Ab] Abstract:Oxalosis is a disease caused by the deposition of calcium oxalate in extrarenal tissues, most commonly bone, myocardium, retina, blood vessels, and skin, causing the clinical manifestations of the disease. Involvement of the blood vessels of the skin can give rise to livedo reticularis, acrocyanosis, ulcers, and gangrene. We present the case of a 60-year-old woman with a history of recurrent renal lithiasis that had led to terminal renal failure requiring hemodialysis and, subsequently, peritoneal dialysis. The patient developed tender red-violaceous skin discoloration of sudden onset, consistent with livedo reticularis; the lesions progressed to form ulcers. Skin biopsy revealed oxalate vasculopathy. In this article we describe the characteristics of this rare disorder, its differentiation from calciphylaxis, and the therapeutic options.
[Mh] MeSH terms primary: Hyperoxaluria/complications
Livedo Reticularis/etiology
[Mh] MeSH terms secundary: Female
Humans
Middle Aged
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1410
[Js] Journal subset:IM
[Da] Date of entry for processing:131028
[St] Status:MEDLINE

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[PMID]: 25317625
[Au] Autor:Almeida JR; Machado Gde A; Santos MM; Lopes Pde F; Matos JP; Neves AC; Lugon JR
[Ad] Address:Universidade Federal Fluminense....
[Ti] Title:Five years results after intrafamilial kidney post-transplant in a case of familial hypomagnesemia due to a claudin-19 mutation.
[So] Source:J Bras Nefrol;36(3):401-5, 2014 Sep.
[Is] ISSN:2175-8239
[Cp] Country of publication:Brazil
[La] Language:eng
[Ab] Abstract:INTRODUCTION: Familial Hypomagnesaemia with hypercalciuria and nephrocalcinosis, with severe ocular impairment secondary to claudin-19 mutation, is a rare recessive autossomic disorder. Its spectrum includes renal Mg2+ wasting, medullary nephrocalcinosis and progressive chronic renal failure in young people. OBJECTIVE: To report a case of kidney transplantation father to daughter in a familial occurrence of severe bilateral nephrocalcinosis associated with ocular impairment in a non-consanguineous Brazilian family, in which two daughters had nephrocalcinosis and severe retinopathy. METHODS: The index case, a 19 years-old female, had long-lasting past medical history of recurrent urinary tract infections, and the abdominal X-ray revealed bilateral multiple renal calcifications as well as ureteral lithiasis, and she was under haemodialysis. She had the diagnosis of retinitis pigmentosa in the early neonatal period. The other daughter (13 years-old) had also nephrocalcinosis with preserved kidney function, retinopathy with severe visual impairment, and in addition, she exhibited hypomagnesaemia = 0.5 mg/dL and hypercalciuria. The other family members (mother, father and son) had no clinical disease manifestation. Mutation analysis at claudin-19 revealed two heterozygous missense mutations (P28L and G20D) in both affected daughters. The other family members exhibited mutant monoallelic status. In despite of that, the index case underwent intrafamilial living donor kidney transplantation (father). CONCLUSION: In conclusion, the disease was characterized by an autosomal recessive compound heterozygous status and, after five years of donation the renal graft function remained stable without recurrence of metabolic disturbances or nephrocalcinosis. Besides, donor single kidney Mg2+ and Ca2+ homeostasis associated to monoallelic status did not affect the safety and the usual living donor post-transplant clinical course.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1410
[Js] Journal subset:IM
[St] Status:In-Data-Review

  5 / 5730 MEDLINE  
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PubMed Central Full text
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[PMID]: 25170197
[Au] Autor:Boraschi P; Donati F
[Ad] Address:Piero Boraschi, Francescamaria Donati, 2 Unit of Radiology, Department of Diagnostic Radiology, Vascular and Interventional Radiology, and Nuclear Medicine, Pisa University Hospital, 56124 Pisa, Italy.
[Ti] Title:Postoperative biliary adverse events following orthotopic liver transplantation: assessment with magnetic resonance cholangiography.
[So] Source:World J Gastroenterol;20(32):11080-94, 2014 Aug 28.
[Is] ISSN:2219-2840
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Biliary adverse events following orthotopic liver transplantation (OLT) are relatively common and continue to be serious causes of morbidity, mortality, and transplant dysfunction or failure. The development of these adverse events is heavily influenced by the type of anastomosis during surgery. The low specificity of clinical and biologic findings makes the diagnosis challenging. Moreover, direct cholangiographic procedures such as endoscopic retrograde cholangiopancreatography and percutaneous transhepatic cholangiography present an inadmissible rate of adverse events to be utilized in clinically low suspected patients. Magnetic resonance (MR) maging with MR cholangiopancreatography is crucial in assessing abnormalities in the biliary system after liver surgery, including liver transplant. MR cholangiopancreatography is a safe, rapid, non-invasive, and effective diagnostic procedure for the evaluation of biliary adverse events after liver transplantation, since it plays an increasingly important role in the diagnosis and management of these events. On the basis of a recent systematic review of the literature the summary estimates of sensitivity and specificity of MR cholangiopancreatography for diagnosis of biliary adverse events following OLT were 0.95 and 0.92, respectively. It can provide a non-invasive method of imaging surgical reconstruction of the biliary anastomoses as well as adverse events including anastomotic and non-anastomotic strictures, biliary lithiasis and sphincter of Oddi dysfunction in liver transplant recipients. Nevertheless, conventional T2-weighted MR cholangiography can be implemented with T1-weighted contrast-enhanced MR cholangiography using hepatobiliary contrast agents (in particular using Gd-EOB-DTPA) in order to improve the diagnostic accuracy in the adverse events' detection such as bile leakage and strictures, especially in selected patients with biliary-enteric anastomosis.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1408
[Js] Journal subset:IM
[St] Status:In-Process
[do] DOI:10.3748/wjg.v20.i32.11080

  6 / 5730 MEDLINE  
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[PMID]: 24814177
[Au] Autor:Remer EM; Herts BR; Primak A; Obuchowski NA; Greiwe A; Roesel DM; Purysko AS; Feldman MK; De S; Shah SN; Dong F; Monga M; Baker ME
[Ad] Address:From the Imaging Institute (E.M.R., B.R.H., N.A.O., A.G., D.M.R., A.S.P., M.K.F., S.N.S., F.D., M.E.B.), Glickman Urological and Kidney Institute (E.M.R., B.R.H., S.D., M.M.), and Department of Quantitative Health Sciences (N.A.O.), Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44195; and Siemens Medical Systems, Malvern, Pa (A.P.).
[Ti] Title:Detection of urolithiasis: comparison of 100% tube exposure images reconstructed with filtered back projection and 50% tube exposure images reconstructed with sinogram-affirmed iterative reconstruction.
[So] Source:Radiology;272(3):749-56, 2014 Sep.
[Is] ISSN:1527-1315
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:PURPOSE: To compare images acquired with 50% tube exposure with a dual-source computed tomographic (CT) scanner and reconstructed with sinogram-affirmed iterative reconstruction (SAFIRE) with 100% exposure images reconstructed with filtered back projection (FBP) for reader ability to detect stones, reader confidence, and findings outside the urinary tract. MATERIALS AND METHODS: In this HIPAA-compliant, institutional review board-approved study, imaging examinations in 99 patients with urolithiasis were assessed. Data from both tubes were reconstructed with FBP; data from the primary tube only were reconstructed with SAFIRE. Seven readers evaluated randomized studies for calculi in nine regions. Reader confidence was scored by using a five-point scale. Ancillary findings were noted. Nonparametric methods for clustered data were used to estimate the area under the receiver operating characteristic curves with 95% confidence intervals to test for noninferiority of 50% exposure with SAFIRE. RESULTS: Calculi were found in 113 locations (pyelocalyceal ureter, 86; proximal ureter, seven; midureter, four; distal ureter, 15; bladder, one) and not found in 752 locations. Mean area under the receiver operating characteristic curve for FBP was 0.879 (range, 0.607-0.967) and for SAFIRE, 0.883 (range, 0.646-0.971; 95% confidence interval: -0.025, 0.031). The SAFIRE images were not significantly inferior to FBP images (P = .001). Reader confidence levels for images with stones were similar with FBP and SAFIRE (P = .963). For the 52 patients who had extraurinary findings, readers reported them correctly in 74.4% (271 of 364) and 72.0% (262 of 364) of cases (P = .215) for FBP and SAFIRE, respectively. For the nine patients with potentially important findings per the reference standard, the detection rates were 44% (28 of 63) and 33% (21 of 63, P = .024), respectively. For the 43 patients with unimportant or likely unimportant findings, the false detection rates were 15% (44 of 301) and 14% (43 of 301, P = .756), respectively. CONCLUSION: The 50% tube exposure CT images reconstructed with SAFIRE were not inferior to 100% exposure images reconstructed with FBP for diagnosis of urolithiasis, without decreases in reader confidence.
[Mh] MeSH terms primary: Algorithms
Information Storage and Retrieval/methods
Radiation Protection/methods
Radiographic Image Interpretation, Computer-Assisted/methods
Tomography, X-Ray Computed/methods
Urolithiasis/radiography
[Mh] MeSH terms secundary: Adult
Aged
Aged, 80 and over
Female
Humans
Male
Middle Aged
Radiation Dosage
Radiographic Image Enhancement/methods
Reproducibility of Results
Sensitivity and Specificity
[Pt] Publication type:COMPARATIVE STUDY; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Em] Entry month:1410
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:140826
[St] Status:MEDLINE
[do] DOI:10.1148/radiol.14132381

  7 / 5730 MEDLINE  
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[PMID]: 23201375
[Au] Autor:Jia J; Shen X; Wang L; Zhang T; Xu M; Fang X; Xu G; Qian C; Wu Y; Geng H
[Ad] Address:Department of Pediatric Urology, Xinhua Hospital, Shanghai Jiao tong University School of Medicine and Children's Urolithiasis Treatment Center of Chinese Ministry of Health, Shanghai, China.
[Ti] Title:Extracorporeal shock wave lithotripsy is effective in treating single melamine induced urolithiasis in infants and young children.
[So] Source:J Urol;189(4):1498-502, 2013 Apr.
[Is] ISSN:1527-3792
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:PURPOSE: We evaluated the safety and efficacy of extracorporeal shock wave lithotripsy in the treatment of single melamine induced urolithiasis in infants and young children. MATERIALS AND METHODS: A total of 189 infants and young children with single melamine induced urolithiasis were referred to our center for treatment with extracorporeal shock wave lithotripsy between March 2009 and July 2010. Location of the calculus was proximal ureteral in 17 patients, mid ureteral in 5, distal ureteral in 26 and kidney in 141. Stone size ranged from 3.8 to 25 mm (mean ± SD 9.79 ± 3.83). RESULTS: All patients underwent extracorporeal shock wave lithotripsy using the same device with an energy ranging from 8 to 12 kV. Stone-free rate was 97.88%, clinically insignificant residual fragment rate was 1.59% and repeat treatment rate was 2.65%. A total of 180 patients (95.24%) required only 1 lithotripsy session and 5 (2.65%) required 2 sessions. Mean ± SD number of shock waves delivered per session was 580.36 ± 190.69 (range 65 to 950). Extracorporeal shock wave lithotripsy failed to fragment stones in only 1 infant, who had a proximal ureteral stone. A total of 181 specimens were collected and analyzed by infrared spectrum, with results demonstrating that the main composition was uric acid and melamine. All patients were followed for a mean of 28 months (range 20 to 36). No severe complication, such as renal subcapsular hemorrhage, hypertension, kidney rupture or lung injury, was observed. CONCLUSIONS: Extracorporeal shock wave lithotripsy with low energy can effectively disintegrate melamine induced calculi. This approach has become our preferred method for treating single melamine induced urolithiasis in infants and young children.
[Mh] MeSH terms primary: Lithotripsy/methods
Resins, Synthetic/adverse effects
Triazines/adverse effects
Urolithiasis/therapy
[Mh] MeSH terms secundary: Child, Preschool
China
Female
Food Contamination
Humans
Infant
Infant Formula/chemistry
Lithotripsy/adverse effects
Lithotripsy/instrumentation
Male
Triazines/analysis
Uric Acid/analysis
Urolithiasis/chemically induced
Urolithiasis/complications
[Pt] Publication type:EVALUATION STUDIES; JOURNAL ARTICLE
[Nm] Name of substance:0 (Resins, Synthetic); 0 (Triazines); 268B43MJ25 (Uric Acid); N3GP2YSD88 (melamine)
[Em] Entry month:1410
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:130408
[St] Status:MEDLINE

  8 / 5730 MEDLINE  
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[PMID]: 25254277
[Au] Autor:Alfonso-Goldfarb AM; Ferraz MH; Rattansi PM
[Ti] Title:Seventeenth-century 'treasure' found in Royal Society archives: the Ludus helmontii and the stone disease.
[So] Source:Notes Rec R Soc Lond;68(3):227-43, 2014 Sep 20.
[Is] ISSN:0035-9149
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Our archival researches at the Royal Society reveal that a small envelope attached to a 1675 letter from an Antwerp apothecary, A. Boutens, contained a sample of the 'Ludus' prepared as a remedy for the 'stone disease' then sweeping through Europe, which was first announced in J. B. van Helmont's De lithiasi (1644). After examining the fascination with the medical use of the Ludus (which required the 'alkahest' for its preparation) and the tenacious efforts to procure it, we trace the fortunae of two other ludi in England, brought to and offered by Francis Mercurius van Helmont during his English sojourn. Both eventually found their way to the geologist John Woodward, one of them through Sir Isaac Newton. Finally we show how the allure of the Ludus helmontii vanished, with transformations in mineral analysis and reclassifications from Woodward to John Hill.
[Mh] MeSH terms primary: Lithiasis/history
Nostrums/history
Urinary Calculi/history
[Mh] MeSH terms secundary: Archives
Belgium
England
History, 17th Century
Lithiasis/prevention & control
Nostrums/analysis
Societies, Scientific
Urinary Calculi/prevention & control
[Pt] Publication type:HISTORICAL ARTICLE; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Name of substance:0 (Nostrums)
[Em] Entry month:1410
[Js] Journal subset:QIS
[Da] Date of entry for processing:140925
[St] Status:MEDLINE

  9 / 5730 MEDLINE  
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[PMID]: 23334384
[Au] Autor:Edvardsson VO; Goldfarb DS; Lieske JC; Beara-Lasic L; Anglani F; Milliner DS; Palsson R
[Ad] Address:The Rare Kidney Stone Consortium, Mayo Clinic, Rochester, MN, USA. vidare@landspitali.is
[Ti] Title:Hereditary causes of kidney stones and chronic kidney disease.
[So] Source:Pediatr Nephrol;28(10):1923-42, 2013 Oct.
[Is] ISSN:1432-198X
[Cp] Country of publication:Germany
[La] Language:eng
[Ab] Abstract:Adenine phosphoribosyltransferase (APRT) deficiency, cystinuria, Dent disease, familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and primary hyperoxaluria (PH) are rare but important causes of severe kidney stone disease and/or chronic kidney disease in children. Recurrent kidney stone disease and nephrocalcinosis, particularly in pre-pubertal children, should alert the physician to the possibility of an inborn error of metabolism as the underlying cause. Unfortunately, the lack of recognition and knowledge of the five disorders has frequently resulted in an unacceptable delay in diagnosis and treatment, sometimes with grave consequences. A high index of suspicion coupled with early diagnosis may reduce or even prevent the serious long-term complications of these diseases. In this paper, we review the epidemiology, clinical features, diagnosis, treatment, and outcome of patients with APRT deficiency, cystinuria, Dent disease, FHHNC, and PH, with an emphasis on childhood manifestations.
[Mh] MeSH terms primary: Adenine Phosphoribosyltransferase/deficiency
Cystinuria/genetics
Dent Disease/genetics
Hypercalciuria/genetics
Hyperoxaluria, Primary/genetics
Kidney Calculi/genetics
Metabolism, Inborn Errors/genetics
Nephrocalcinosis/genetics
Renal Insufficiency, Chronic/genetics
Renal Tubular Transport, Inborn Errors/genetics
Urolithiasis/genetics
[Mh] MeSH terms secundary: Adenine Phosphoribosyltransferase/genetics
Animals
Child
Cystinuria/diagnosis
Cystinuria/epidemiology
Cystinuria/therapy
Dent Disease/diagnosis
Dent Disease/epidemiology
Dent Disease/therapy
Genetic Predisposition to Disease
Heredity
Humans
Hypercalciuria/diagnosis
Hypercalciuria/epidemiology
Hypercalciuria/therapy
Hyperoxaluria, Primary/diagnosis
Hyperoxaluria, Primary/epidemiology
Hyperoxaluria, Primary/therapy
Kidney Calculi/diagnosis
Kidney Calculi/epidemiology
Kidney Calculi/therapy
Metabolism, Inborn Errors/diagnosis
Metabolism, Inborn Errors/epidemiology
Metabolism, Inborn Errors/therapy
Nephrocalcinosis/diagnosis
Nephrocalcinosis/epidemiology
Nephrocalcinosis/therapy
Phenotype
Prognosis
Renal Insufficiency, Chronic/diagnosis
Renal Insufficiency, Chronic/epidemiology
Renal Insufficiency, Chronic/therapy
Renal Tubular Transport, Inborn Errors/diagnosis
Renal Tubular Transport, Inborn Errors/epidemiology
Renal Tubular Transport, Inborn Errors/therapy
Risk Factors
Urolithiasis/diagnosis
Urolithiasis/epidemiology
Urolithiasis/therapy
[Pt] Publication type:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, NON-U.S. GOV'T; REVIEW
[Nm] Name of substance:EC 2.4.2.7 (Adenine Phosphoribosyltransferase)
[Em] Entry month:1403
[Cu] Class update date: 141012
[Lr] Last revision date:141012
[Js] Journal subset:IM
[Da] Date of entry for processing:130826
[St] Status:MEDLINE
[do] DOI:10.1007/s00467-012-2329-z

  10 / 5730 MEDLINE  
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[PMID]: 24684546
[Au] Autor:Kang HW; Lee SK; Kim WT; Kim YJ; Yun SJ; Lee SC; Kim WJ
[Ad] Address:Department of Urology, Chungbuk National University , College of Medicine and Institute for Tumor Research, Cheongju, South Korea .
[Ti] Title:Hypertriglyceridemia and low high-density lipoprotein cholesterolemia are associated with increased hazard for urolithiasis.
[So] Source:J Endourol;28(8):1001-5, 2014 Aug.
[Is] ISSN:1557-900X
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:PURPOSE: To assess the association between dyslipidemia and urolithiasis, a propensity score-matching study was performed. PATIENTS AND METHODS: Fasting blood samples were taken, and serum lipid profiles were measured in 655 stone formers (SF) and 1965 propensity score-matched controls between 2005 and 2011. The controls, from a health-screening program, did not have a history of dyslipidemia or statin use and have any evidence of stone disease, as determined by abdominal radiography, ultrasonography examination. Propensity score-matching with respect to age, sex, and body mass index was used to minimize selection bias, and the logistic regression analysis was adjusted for other components of metabolic syndrome. RESULTS: Compared with controls, the SF group had significantly higher mean triglyceride and lower total cholesterol, low-density lipoprotein (LDL) cholesterol, and high-density lipoprotein (HDL) cholesterol levels (each P<0.001). The SF group was also more likely to have hypertriglyceridemia and low HDL-cholesterolemia, and less likely to have hypercholesterolemia and high LDL cholesterolemia compared with controls (each P<0.05). When adjusted for other components of metabolic syndrome including obesity, presence of diabetes mellitus or hypertension, the odds ratio (OR) for urinary stones appeared with hypercholesterolemia (OR=0.747, P=0.003), hypertriglyceridemia (OR=1.901, P<0.001), low HDL cholesterolemia (OR=1.886, P<0.001) and high LDL cholesterolemia (OR=0.610, P<0.001). CONCLUSIONS: Our study implies that dyslipidemia may play a crucial part in urinary stone risk.
[Mh] MeSH terms primary: Hypertriglyceridemia/complications
Hypolipoproteinemias/complications
Lipoproteins, HDL/blood
Urolithiasis/etiology
[Mh] MeSH terms secundary: Adolescent
Adult
Aged
Body Mass Index
Case-Control Studies
Cholesterol/blood
Fasting/blood
Female
Humans
Hypertriglyceridemia/blood
Male
Middle Aged
Odds Ratio
Propensity Score
Regression Analysis
Retrospective Studies
Risk Factors
Urolithiasis/drug therapy
Young Adult
[Pt] Publication type:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Name of substance:0 (Lipoproteins, HDL); 97C5T2UQ7J (Cholesterol)
[Em] Entry month:1410
[Js] Journal subset:IM
[Da] Date of entry for processing:140731
[St] Status:MEDLINE
[do] DOI:10.1089/end.2014.0135


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