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61.
  • Cunha, Pedro G, et al. (författare)
  • Pulse wave velocity distribution in a cohort study: from arterial stiffness to early vascular aging.
  • 2015
  • Ingår i: Journal of Hypertension. - 1473-5598. ; 33:7, s. 1438-1445
  • Tidskriftsartikel (refereegranskat)abstract
    • By contrast with other southern European people, north Portuguese population registers an especially high prevalence of hypertension and stroke incidence. We designed a cohort study to identify individuals presenting accelerated and premature arterial aging in the Portuguese population.
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63.
  • Dahlberg, Jonas, et al. (författare)
  • Genetic variants in serum and glucocortocoid regulated kinase 1, a regulator of the epithelial sodium channel, are associated with ischaemic stroke.
  • 2011
  • Ingår i: Journal of Hypertension. - 1473-5598. ; 29, s. 884-889
  • Tidskriftsartikel (refereegranskat)abstract
    • OBJECTIVE: Serum and glucocorticoid regulated kinase 1 (SGK1) expression is increased by aldosterone and is a key regulator of the amiloride-sensitive sodium channel (ENaC) in the distal nephron. We have previously shown that two SNPs in SGK1 (rs1057293 and rs1743966) are associated with blood pressure variation and blood pressure progression in the general population. Therefore, we tested the association of these variants with ischaemic stroke. METHODS: Using logistic regression, we analysed rs1057293 and rs1743966 for association with ischaemic stroke in two independent age-matched and sex-matched case-control groups from the twin cities of Lund (cases n = 1837 and controls n = 947) and Malmö (cases n = 888 and controls n = 893) in the Scania region of southern Sweden. RESULTS: In additive models adjusted for hypertension, smoking and diabetes, the major allele (G) of rs1057293 was associated (odds ratio, 95% confidence interval; P value) with ischaemic stroke with similar effect size in both studies; in Lund (1.35, 1.11-1.64; P = 0.002) and Malmö (1.30, 1.03-1.65; P = 0.027). When the two studies were pooled, the overall association was 1.32, 1.14-1.52; P < 0.001. The major allele of rs1743966 (A), which was in linkage disequilibrium with rs1057293, showed a similar trend as rs1057293 G-allele but with slightly weaker effect size and P value. CONCLUSION: In two independent but ethnically similar populations, we observed an association between genetic variants in SGK1 and ischaemic stroke. Interestingly, the association seems to be at least partially independent of blood pressure. This could imply that cerebrovascular ENaC or other SGK1-regulated proteins may be of importance for development of ischaemic stroke.
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68.
  • Du Toit, Jacques D., et al. (författare)
  • Estimating population level 24-h sodium excretion using spot urine samples in older adults in rural South Africa
  • 2023
  • Ingår i: Journal of Hypertension. - : Wolters Kluwer. - 0263-6352 .- 1473-5598. ; 41:2, s. 280-287
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: South Africa has introduced regulations to reduce sodium in processed foods. Assessing salt consumption with 24-h urine collection is logistically challenging and expensive. We assess the accuracy of using spot urine samples to estimate 24-h urine sodium (24hrUNa) excretion at the population level in a cohort of older adults in rural South Africa.METHODS: 24hrUNa excretion was measured and compared to that estimated from matched spot urine samples in 399 individuals, aged 40-75 years, from rural Mpumalanga, South Africa. We used the Tanaka, Kawasaki, International Study of Sodium, Potassium, and Blood Pressure (INTERSALT), and Population Mean Volume (PMV) method to predict 24hrUNa at the individual and population level.RESULTS: The population median 24hrUNa excretion from our samples collected in 2017 was 2.6 g (interquartile range: 1.53-4.21) equal to an average daily salt intake of 6.6 g, whereas 65.4% of participants had a salt excretion above the WHO recommended 5 g/day. Estimated population median 24hrUNa derived from the INTERSALT, both with and without potassium, showed a nonsignificant difference of 0.25 g (P = 0.59) and 0.21 g (P = 0.67), respectively. In contrast, the Tanaka, Kawasaki, and PMV formulas were markedly higher than the measured 24hrUNa, with a median difference of 0.51 g (P = 0.004), 0.99 g (P = 0.00), and 1.05 g (P = 0.00) respectively. All formulas however performed poorly when predicting an individual's 24hrUNa.CONCLUSION: In this population, the INTERSALT formulas are a well suited and cost-effective alternative to 24-h urine collection for the evaluation of population median 24hrUNa excretion. This could play an important role for governments and public health agencies in evaluating local salt regulations and identifying at-risk populations.
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69.
  • Edlinger, Michael, et al. (författare)
  • Blood pressure and other metabolic syndrome factors and risk of brain tumour in the large population-based Me-Can cohort study
  • 2012
  • Ingår i: Journal of Hypertension. - 0263-6352 .- 1473-5598. ; 30:2, s. 290-296
  • Tidskriftsartikel (refereegranskat)abstract
    • OBJECTIVES:: Brain tumour has few established determinants. We assessed to which extent risk of brain tumour was related to metabolic syndrome factors in adults. METHODS:: In the Me-Can project, 580 000 individuals from Sweden, Austria, and Norway were followed for a median of 10 years after baseline measurement. Data on brain tumours were obtained from national cancer registries. The factors of metabolic syndrome (BMI, SBP and DBP, and blood levels of glucose, cholesterol, and triglycerides), separately and combined, were analysed in quintiles and for transformed z-scores (mean transformed to 0 and standard deviation to 1). Cox proportional hazards multivariate regression models were used, with corrections for measurement error. RESULTS:: During follow-up, 1312 primary brain tumours were diagnosed, predominantly meningioma (n = 348) and high-grade glioma (n = 436). For meningioma, the hazard ratio was increased for z-scores of SBP [hazard ratio = 1.27 per unit standard deviation, 95% confidence interval (CI) 1.03-1.57], of DBP (hazard ratio = 1.29, 95% CI 1.04-1.58), and of the combined metabolic syndrome score (hazard ratio = 1.31, 95% CI 1.11-1.54). An increased risk of high-grade glioma was found for DBP (hazard ratio = 1.23, 95% CI 1.01-1.50) and triglycerides (hazard ratio = 1.35, 95% CI 1.05-1.72). For both meningioma and high-grade glioma, the risk was more than double in the fifth quintiles of DBP compared to the lowest quintile. For meningioma this risk was even larger for SBP. CONCLUSION:: Increased blood pressure was associated with risk of brain tumours, especially of meningiomas.
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70.
  • Eiken, Ola, et al. (författare)
  • Repeated exposures to moderately increased intravascular pressure increases stiffness in human arteries and arterioles
  • 2011
  • Ingår i: Journal of Hypertension. - 0263-6352 .- 1473-5598. ; 29:10, s. 1963-1971
  • Tidskriftsartikel (refereegranskat)abstract
    • The aim was to investigate whether repeated exposures to moderate pressure elevations in the blood vessels of the arms (pressure training; PT) affect pressure distension in arteries/arterioles of healthy subjects (n=11). PT and vascular pressure-distension determinations were conducted with the subject seated in a pressure chamber with one arm slipped through a hole in the chamber door. Increased intravascular pressure was accomplished by increasing chamber pressure. Before PT, one arm was investigated (control arm) during stepwise increases in chamber pressure to 180 mmHg. Artery diameter and flow were measured in the brachial artery using ultrasonography/Doppler techniques. Thereafter, the contralateral arm underwent a PT regimen consisting of three 40 min sessions/ week during 5 weeks. Chamber pressure was increased during PT from 65 mmHg during the first week to 105 mmHg during the last week. After PT, pressure-distension relationships were examined in both the trained arm and the control arm. Prior to and following PT, endothelium-dependent and endothelium-independent dilatations of the brachial artery were studied. PT reduced (p<0.01) arterial pressure distension by 46 ± 18%. Likewise, the pressure-induced increase in arterial flow was less pronounced after (350 ± 249%) compared with before (685 ± 216 %) PT. The PT-induced reductions in arterial/arteriolar pressure distension were reversed 5 weeks post-PT. Neither endothelium-dependent nor endothelium-independent arterial dilatation were affected by PT. It thus appears that the in vivo wall stiffness in arteries and arterioles increases markedly in response to intermittent, moderate increments of transmural pressure during 5 weeks. The increases in arterial/arteriolar stiffness are reversible and do not reflect a reduced capacity to dilate the vessels. The findings are compatible with the notion that local load serves as “ a prime mover” in the development of vascular changes in hypertension.
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