The DOI matches its Crossref record; 74 of the 74 references it cites were found in a registry or an index.
Cardiovascular abnormalities in autosomal-dominant polycystic kidney disease
Open accessAbstract
Cardiovascular problems are a major cause of morbidity and mortality in patients with autosomal-dominant polycystic kidney disease (ADPKD). Hypertension is a common early symptom of ADPKD, and occurs in approximately 60% of patients before renal function has become impaired. Hypertension is associated with an increased rate of progression to end-stage renal disease and is the most important potentially treatable variable in ADPKD. Left ventricular hypertrophy, which is a powerful, independent risk factor for cardiovascular morbidity and mortality, also occurs frequently in patients with ADPKD. Both hypertension and left ventricular hypertrophy have important roles in cardiovascular complications in these individuals. Moreover, biventricular diastolic dysfunction, endothelial dysfunction, increased carotid intima–media thickness, and impaired coronary flow velocity reserve are present even in young patients with ADPKD who have normal blood pressure and well-preserved renal function. These findings suggest that cardiovascular involvement starts very early in the course of ADPKD. Intracranial and extracranial aneurysms and cardiac valvular defects are other potential cardiovascular problems in patients with ADPKD. Early diagnosis and treatment of hypertension, with drugs that block the renin–angiotensin–aldosterone system, has the potential to decrease the cardiovascular complications and slow the progression of renal disease in ADPKD.
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Circadian blood pressure changes and left ventricular hypertrophy in essential hypertension.
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Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease
Gabow, P. A., Johnson, A. M., Kaehny, W. D., Kimberling, W. J., Lezotte, D. C., Duley, I. T., & Jones, R. H. (1992) · Kidney International · doi:10.1038/ki.1992.195 · Cited by 509
The Renin–Angiotensin–Aldosterone System and Autosomal Dominant Polycystic Kidney Disease
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Self-citationDiseases of the kidney and urinary tract
Schrier, R. W. (2001) · Cited by 396
Self-citationCauses of death in autosomal dominant polycystic kidney disease.
Fick, G. M., Johnson, A. M., Hammond, W. S., & Gabow, P. A. (1995) · Journal of the American Society of Nephrology · doi:10.1681/asn.v5122048 · Cited by 342
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Sympathetic Activity Is Increased in Polycystic Kidney Disease and Is Associated with Hypertension
KLEIN, I. H. H. T., LIGTENBERG, G., OEY, P. L., KOOMANS, H. A., & BLANKESTIJN, P. J. (2001) · Journal of the American Society of Nephrology · doi:10.1681/asn.v12112427 · Cited by 248
Cited by
Kou, P., Wei, S., & Xiong, F. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867325666180330094434 · Cited by 6
Metadata
- Authors
- Ecder, T., & Schrier, R. W.
- Venue
- Nature Reviews Nephrology
- Published
- 2009-04
- Volume
- 5
- Issue
- 4
- Pages
- 221-228
- ISSN
- 1745-8323 (ISSN-L)
- 1759-5061
- 1759-507X
- OpenAlex
- W2030927065
- Cited by
- 275
- References
- 74
- FWCI
- 1.15
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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