Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0085580 (essential hypertension)
14,686 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Although angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) belong to a family of therapies that block the renin-angiotensin system and are suggested to improve proteinuria/albuminuria, it is unclear which is more effective. To compare the effects of ACEIs and ARBs on proteinuria in primary hypertension by performing a meta-analysis covering randomized controlled trials (RCTs). We systematically searched MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials from January 1990 to November 2014. Eligible studies were RCTs of ACEI therapy versus ARB therapy that reported the albumin excretion rate (AER), albumin (Alb), and urinary albumin excretion (UAE) as outcomes. Seventeen RCTs, including 17,951 patients (without limit of race, age, or sex) with a mean duration of 62.6 weeks, were included. Pooled analysis suggested that ACEIs and ARBs showed no significant differences in AER/Alb/UAE/24-h urine protein/24-h urine total protein in a comparison of 10 trials (SMD 0.09; 95% CI -0.18-0.36; P = 0.52). No significant differences were observed in urinary protein/creatinine ratio (UPCR)/urinary albumin/creatinine ratio (UACR), or albumin/creatinine ratio (ACR) in 7 trials (SMD 0.15; 95% CI -1.88-2.19; P = 0.88). The total outcome of ACEIs and ARBs also showed no significant difference (SMD 0.13; 95% CI -1.03-1.29; P = 0.83). The efficacies of ACEIs and ARBs in controlling blood pressure as a secondary indicator were also similar (SMD -0.50; 95% CI -1.58-0.58; P = 0.37). Based on a meta-analysis of 17 randomized controlled trials including 17,951 patients, we found that ACEIs and ARBs can reduce urine protein levels, improve blood pressure, and were similarly effective in terms of reducing urinary protein excretion.
...
PMID:Effects of ACEIs Versus ARBs on Proteinuria or Albuminuria in Primary Hypertension: A Meta-Analysis of Randomized Trials. 2642 27

Primary aldosteronism (PA) represents major cause of secondary hypertension, strongly associated with high cardiovascular morbidity and mortality. Aldosterone excess may influence mineral homeostasis, through higher urinary calcium (Ca) excretion reducing calcium plasma levels and leading to secondary increase of parathyrine (PTH). The purpose of the present study is to clarify the association of serum PTH and Ca levels with PA using a metaanalysis approach. We searched articles indexed in the PubMed, OVID and Sciencedirect published as of September 2014 that met our predefined criteria. Six articles with 748 subjects from 8 case-control studies were identified. Overall, pooled analysis indicated that subjects with PA had higher serum PTH concentrations and lower Ca levels than controls with essential hypertension (EH) (PTH: SMD = 1.146, 95% CI = [0.774, 1.518]; Ca: SMD = -0.698, 95% CI = [-1.102,-0.294]). Further subgroup analysis stratified by geological location found a similar pattern both in Italy and Austria (Italy: for PTH, SMD = 1.176, 95% CI = [0.758, 1.593], for Ca, SMD = -0.669, 95% CI = [-1.119,-0.219]; Austria: for PTH, SMD = 1.004, 95% CI = [0.359, 1.648], for Ca, SMD = -0.900, 95% CI = [-1.543,-0.257]). In addition, the subgroup analysis stratified by type of Ca measurement also found a similar pattern by spectrophotometry (SMD = -1.078, 95% CI = [-1.532, -0.623]), but not by ion selective electrode (SMD = -0.248, 95% CI = [-0.810, 0.315]). Sensitivity analysis showed that excluding any one study from the pooled analysis did not vary the results substantially. No evidence of publication bias was observed. In conclusion, this meta-analysis supports a significant association of PTH and Ca concentration with PA. Therefore, the high levels of PTH and low Ca concentrations in serum can be used as a variable predictor for PA.
...
PMID:Association of serum parathyrine and calcium levels with primary aldosteronism: a meta-analysis. 2662 45