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Biomedical subjects

E Krieger

Publications and source records attributed to E Krieger.

At least 19 recordsLinked to original sources
PubMed2005

Carotid intima-media thickness, carotid wall shear stress and restenosis after femoro-popliteal percutaneous transluminal angioplasty (PTA).

OBJECTIVE: To determine the relationship between carotid intima-media thickness (IMT), carotid wall shear stress (WSS) and restenosis after femoro-popliteal percutaneous transluminal angioplasty (PTA). PATIENTS AND METHODS: Thirty-one subjects (18 men, 13 women, median age 69 years) treated with femoro-popliteal PTA for symptomatic peripheral arterial occlusive disease were enrolled. On admission, IMT, internal diameter and blood velocity of the common carotid artery (CCA) were assessed by high-resolution ultrasonography. Blood viscosity was measured and carotid WSS was calculated. Patients were followed up for 6 months for the occurrence of significant restenosis (>50%) as documented by duplex ultrasonography. Two patients were lost to follow-up. RESULTS: Fourteen patients (48%) developed restenosis at 6 months. IMT and WSS were not different in patients without and with restenosis (IMT: 0.90 (0.85-0.97) vs. 0.89 (0.84-0.93) mm, p = 0.51; WSS: 14.1 (11.9-19.2) vs. 15.9 (12.8-21.5) dyne/cm2, p = 0.48). The hazard ratio of incident restenosis as estimated by Cox regression analysis was 0.04 for IMT (p = 0.23; 95% CI 0.0001-8.22) and 1.07 for WSS (p = 0.10; 95% CI 0.98-1.17). CONCLUSIONS: In this pilot study involving a limited number of patients, carotid IMT and carotid WSS are not significantly related to restenosis at 6 months after femoro-popliteal PTA. This might be the result of different underlying pathophysiology for atherosclerosis and restenosis.

Aged↗
PubMed2004

High wall shear stress measured by magnetic resonance is a predictor of restenosis in the femoral-artery after balloon angioplasty.

AIM: Wall shear stress (WSS) has been implied in the pathogenesis of restenosis after percutaneous transluminal angioplasty (PTA). Aims of the present study were to calculate WSS in the superficial femoral artery (SFA) from magnetic resonance imaging (MRI) and from duplex sonography in healthy controls and in patients after PTA of the SFA to evaluate the predictive value of WSS for restenosis. METHODS: WSS was assessed by calculating the slope of velocity profiles at the vessel wall from data obtained with velocity encoded cine MR and with duplex using the formula: Shear stress=4xblood viscosityxpeak blood velocity/internal diameter. Seventeen patients were studied 1 day after successful PTA of the SFA. Restenosis was determined by duplex ultrasound at the 6-months follow-up visit. RESULTS: In healthy controls WSS values calculated from MRI and from duplex were similar (1.86+/-0.35 N/m2 vs 1.88+/-0.34 N/m2, n.s.). In patients the values obtained with duplex were higher than those obtained with MRI (4.1+/-2.3 N/m2 vs 2.4+/-1.2 N/m2, p=0.002). With both methods post-interventional WSS was higher in patients developing restenosis (duplex 5.4+/-2.2 N/m2, MRI 3.1+/-0.9 N/m2) than in those without restenosis (duplex 2.7+/-1.4 N/m2, MRI 1.5+/-0.7 N/m2) and was revealed to be an independent predictor of restenosis (p=0.03). CONCLUSIONS: This is the first study demonstrating that increased post-interventional WSS in the SFA is predictive for restenosis. WSS values obtained with MRI and duplex were different in patients, however with both methods higher WSS was associated with restenosis.

Adult↗
PubMed2003

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism.

Four chromosomal loci ( PARK2, PARK6, PARK7, and PARK9) associated with autosomal recessive, early onset parkinsonism are known. We mapped the PARK7 locus to chromosome 1p36 in a large family from a genetically isolated population in the Netherlands, and confirmed this linkage in an Italian family. By positional cloning within the refined PARK7 critical region we recently identified mutations in the DJ-1 gene in the two PARK7-linked families. The function of DJ-1 remains largely unknown, but evidence from genetic studies on the yeast DJ-1 homologue, and biochemical studies in murine and human cell lines, suggests a role for DJ-1 as an antioxidant and/or a molecular chaperone. Elucidating the role of DJ-1 will lead to a better understanding of the pathogenesis of DJ-1-related and common forms of Parkinson's disease.

Chromosomes, Human, Pair 1↗
PubMed2003

A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).

Linkage analysis in a multigenerational family with autosomal dominant hearing loss yielded a chromosomal localisation of the underlying genetic defect in the DFNA20/26 locus at 17q25-qter. The 6-cM critical region harboured the gamma-1-actin (ACTG1) gene, which was considered an attractive candidate gene because actins are important structural elements of the inner ear hair cells. In this study, a Thr278Ile mutation was identified in helix 9 of the modelled protein structure. The alteration of residue Thr278 is predicted to have a small but significant effect on the gamma 1 actin structure owing to its close proximity to a methionine residue at position 313 in helix 11. Met313 has no space in the structure to move away. Moreover, the Thr278 residue is highly conserved throughout eukaryotic evolution. Using a known actin structure the mutation could be predicted to impair actin polymerisation. These findings strongly suggest that the Thr278Ile mutation in ACTG1 represents the first disease causing germline mutation in a cytoplasmic actin isoform.

Actins↗
PubMed2000

Arm placement of the Cook titanium Petite Vital-Port: results of radiologic placement in 125 patients with cancer.

OBJECTIVE: Patients with cancer require reliable venous access for therapy and phlebotomy. Traditionally, insertion of venous ports has been performed in the operating room. However, the interventional radiology service has recently become involved in the placement of a variety of venous access devices. This study examines the technique and complications associated with the placement of venous ports in the arm for patients with cancer. METHODS: Cook titanium Petite Vital-Ports (Cook Canada, Stouffville, Ont.) were implanted in patients with cancer, and implantation was performed in the medical imaging vascular/interventional suite. Patients were followed prospectively by periodic chart review for a maximum of 42 months after port insertion. Minimum follow-up in patients who did not die from cancer was 6 months. RESULTS: The authors implanted 125 Vital-Ports. The mean duration of port implantation was 265 days (range 2 to 1278 days, total catheter days 33 221). Venous thrombosis developed in 5 patients (4%, or 0.06 episodes/1000 catheter days). Four patients (3.2%, or 0.12 episodes/1000 catheter days) had suspected infection of the port or catheter, and 2 had culture-positive infection (1.6%, or 0.06 episodes/1000 catheter days). Two patients (1.6%, or 0.06 episodes/1000 catheter days) required port or catheter revision owing to mechanical difficulties. CONCLUSION: The Cook titanium Petite Vital-Port, implanted in the arm in the medical imaging vascular/interventional suite, is relatively safe and effective. As a result, it has been widely accepted by the patients and clinicians at the hospital where this study was conducted.

Adult↗
PubMed1999

Left ventricular hypertrophy predicts outcome of hypertension regardless of the type of ventricular arrhythmia present.

Left ventricular hypertrophy is associated with an increased cardiovascular mortality in hypertension. A potential role of ventricular arrhythmias is debated but not yet determined. The purpose of this study was to evaluate whether the presence of arrhythmias would ascribe any additional risk to cardiovascular mortality beyond that related to the presence of left ventricular hypertrophy. From November 1988 to February 1991, 40 mild to severe hypertensive patients (mean SBP, DBP 183/117 mm Hg) were submitted to clinical, echocardiographic and electrocardiographic evaluations complemented by 24-h Holter monitoring and then followed until November 1996. The Kaplan-Meier method supplemented by the Cox multiple regression model were performed to identify the variable(s) associated with fatal cardiovascular outcome. Twelve cardiovascular fatalities occurred as a consequence of sudden death (n = 4), stroke (n = 4), heart failure (n = 2) and myocardial infarction (n = 2). In comparison with patients who survived, those dying from cardiovascular causes had a greater percentage of electrocardiographic left ventricular hypertrophy (83 vs 36%, P = 0. 0037) and couplets of ventricular ectopic beats (58 vs 18%, P = 0. 0467). In addition, they showed larger left ventricular diastolic diameter (60 +/- 10 vs 53 +/- 8 mm), mass index (248 +/- 67 vs 154 +/- 57 g/m2) and posterior wall thickness (12 +/- 2 vs 10 +/- 2 mm), as well as shorter left ventricular fractional shortening (0.23 +/- 0.8 vs 0.32 +/- 0.9). Univariate analysis showed that electrocardiographic left ventricular hypertrophy and strain, mass index, end-systolic wall stress, fractional shortening and the presence of couplets were significantly related to cardiovascular mortality. However, only mass index was shown to be independently associated with cardiovascular death. In conclusion, left ventricular hypertrophy predicts cardiovascular outcome, regardless of the presence of other signs of cardiac damage, including ventricular arrhythmia.

Adult↗
PubMed1977

[Inhalation therapy in respiratory diseases (author's transl)].

The various techniques for aerosol therapy are described, as applied to inflammations of the upper and lower airways. Advances in treatment include dinatrium cromoglicicum and beclomethasone-dipropionate, with the latter medication improving results in patients with allergic reactions of the nasal and bronchial mucosa.

Adrenal Cortex Hormones↗