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Article: Cardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney disease

TitleCardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney disease
Authors
Issue Date2011
Citation
Clinical Journal of the American Society of Nephrology, 2011, v. 6, n. 10, p. 2508-2515 How to Cite?
AbstractBackground and objectives: Autosomal dominant polycystic kidney disease (ADPKD) is associated with a substantial cardiovascular disease burden including early onset hypertension, intracranial aneurysms, and left ventricular hypertrophy (LVH). A 41% prevalence of LVH has been reported in ADPKD, using echocardiographic assessment of LV mass (LVM). The HALT PKD study was designed to assess the effect of intensive angiotensin blockade on progression of total kidney volume and LVM. Measurements of LVM were performed using cardiac magnetic resonance (MR). Design, setting, participants, & measurements: Five hundred forty-three hypertensive patients with GFR >60 ml/min per 1.73 m2 underwent MR assessment of LVM at baseline. LVM was adjusted for body surface area and expressed as LVM index (LVMI; g/m2). Results: Baseline BP was 125.1 ± 14.5/79.3 ± 11.6 mmHg. Average duration of hypertension was 5.79 years. Prior use of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers was present in 59.5% of patients. The prevalence of LVH assessed using nonindexed LVM (g) was 3.9% (n = 21, eight men and 13 women) and 0.93% (n = 5, one man and four women) using LVMI (g/m2). In exploratory analyses, the prevalence of LVH using LVM indexed to H2.7, and the allometric index ppLVmassHW, ranged from 0.74% to 2.23% (n = 4 to 12). Multivariate regression showed significant direct associations of LVMI with systolic BP, serum creatinine, and albuminuria; significant inverse associations with LVMI were found with age and female gender. Conclusions: The prevalence of LVH in hypertensive ADPKD patients <50 years of age with short duration of hypertension, and prior use of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers is low. Early BP intervention in ADPKD may have decreased LVH and may potentially decrease cardiovascular mortality. © 2011 by the American Society of Nephrology.
Persistent Identifierhttp://hdl.handle.net/10722/316055
ISSN
2021 Impact Factor: 10.614
2020 SCImago Journal Rankings: 2.755
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPerrone, Ronald D.-
dc.contributor.authorAbebe, Kaleab Z.-
dc.contributor.authorSchrier, Robert W.-
dc.contributor.authorChapman, Arlene B.-
dc.contributor.authorTorres, Vicente E.-
dc.contributor.authorBost, James-
dc.contributor.authorKaya, Diana-
dc.contributor.authorMiskulin, Dana C.-
dc.contributor.authorSteinman, Theodore I.-
dc.contributor.authorBraun, William-
dc.contributor.authorWinklhofer, Franz T.-
dc.contributor.authorHogan, Marie C.-
dc.contributor.authorRahbari-Oskoui, Frederic-
dc.contributor.authorKelleher, Cass-
dc.contributor.authorMasoumi, Amirali-
dc.contributor.authorGlockner, James-
dc.contributor.authorHalin, Neil J.-
dc.contributor.authorMartin, Diego-
dc.contributor.authorRemer, Erick-
dc.contributor.authorPatel, Nayana-
dc.contributor.authorPedrosa, Ivan-
dc.contributor.authorWetzel, Louis H.-
dc.contributor.authorThompson, Paul A.-
dc.contributor.authorMiller, J. Philip-
dc.contributor.authorMeyers, Catherine M.-
dc.contributor.authorBae, K. Ty-
dc.date.accessioned2022-08-24T15:49:05Z-
dc.date.available2022-08-24T15:49:05Z-
dc.date.issued2011-
dc.identifier.citationClinical Journal of the American Society of Nephrology, 2011, v. 6, n. 10, p. 2508-2515-
dc.identifier.issn1555-9041-
dc.identifier.urihttp://hdl.handle.net/10722/316055-
dc.description.abstractBackground and objectives: Autosomal dominant polycystic kidney disease (ADPKD) is associated with a substantial cardiovascular disease burden including early onset hypertension, intracranial aneurysms, and left ventricular hypertrophy (LVH). A 41% prevalence of LVH has been reported in ADPKD, using echocardiographic assessment of LV mass (LVM). The HALT PKD study was designed to assess the effect of intensive angiotensin blockade on progression of total kidney volume and LVM. Measurements of LVM were performed using cardiac magnetic resonance (MR). Design, setting, participants, & measurements: Five hundred forty-three hypertensive patients with GFR >60 ml/min per 1.73 m2 underwent MR assessment of LVM at baseline. LVM was adjusted for body surface area and expressed as LVM index (LVMI; g/m2). Results: Baseline BP was 125.1 ± 14.5/79.3 ± 11.6 mmHg. Average duration of hypertension was 5.79 years. Prior use of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers was present in 59.5% of patients. The prevalence of LVH assessed using nonindexed LVM (g) was 3.9% (n = 21, eight men and 13 women) and 0.93% (n = 5, one man and four women) using LVMI (g/m2). In exploratory analyses, the prevalence of LVH using LVM indexed to H2.7, and the allometric index ppLVmassHW, ranged from 0.74% to 2.23% (n = 4 to 12). Multivariate regression showed significant direct associations of LVMI with systolic BP, serum creatinine, and albuminuria; significant inverse associations with LVMI were found with age and female gender. Conclusions: The prevalence of LVH in hypertensive ADPKD patients <50 years of age with short duration of hypertension, and prior use of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers is low. Early BP intervention in ADPKD may have decreased LVH and may potentially decrease cardiovascular mortality. © 2011 by the American Society of Nephrology.-
dc.languageeng-
dc.relation.ispartofClinical Journal of the American Society of Nephrology-
dc.titleCardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney disease-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.2215/CJN.04610511-
dc.identifier.pmid21903983-
dc.identifier.scopuseid_2-s2.0-80053923405-
dc.identifier.volume6-
dc.identifier.issue10-
dc.identifier.spage2508-
dc.identifier.epage2515-
dc.identifier.eissn1555-905X-
dc.identifier.isiWOS:000295657000026-

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