Cardiovascular risk factors and the impact on prognosis in patients with chronic kidney disease secondary to autosomal dominant polycystic kidney disease


Por: Gorriz, JL, Arroyo, D, D'Marco, L, Torra, R, Tomas, P, Puchades, MJ, Panizo, N, Pantoja, J, Montomoli, M, Llisterri, JL, Pallares-Carratala, V, Valdivielso, JM

Publicada: 25 mar 2021
Resumen:
BackgroundAutosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease. There is an increased rate of cardiovascular disease (CVD) in ADPKD. In this study, we evaluate the prevalence of cardiovascular risk factors, the achievement rates for treatment goals and cardiovascular events (CVE) in ADPKD and their relations with asymptomatic CVD in CKD from other etiologies (CKDoe) and controls.MethodsWe evaluated 2445 CKD patients (2010-2012). The information collected was: clinical, anthropometric and analytical parameters, treatments and CVD evaluation (intima-media thickness (IMT), atheromatous plaque presence and ankle-brachial index (ABI)). Laboratory, vital status, CVE and hospitalizations were collected for 4years.ResultsADPKD patients had a worse renal function and worst achievement of blood pressure, higher parathormone levels but lower proteinuria compared to CKDoe. ADPKD patients presented lower IMT values than other groups, however, an intermediate rate of pathologic ABI and atheromatous plaque was present. More than half of the patients received statins, achieving LDL-c levels <100 only in 50 and 39.8% of them (ADPKD and CKDoe respectively). The number of CVE during the follow-up period was low. In adjusted Cox regression model, ADPDK had the lowest occurrence of CVE of all three groups (HR:0.422, 95%CI 0.221-0.808, p =0.009).ConclusionADPKD patients show intermediate control rates of CVD. A better control of CVD risk seems to be related with a lower load of CVD compared to other groups, which may lead in the long term to a better prognosis. Further investigation is necessary to determine cardiovascular prognosis in ADPKD.

Filiaciones:
Gorriz, JL:
 Univ Valencia, Univ Clin Hosp, INCLIVA, Dept Nephrol, Av Blasco Ibanez 17, Valencia 46010, Spain

Arroyo, D:
 Hosp Gen Univ Gregorio Maranon, Dept Nephrol, Madrid, Spain

D'Marco, L:
 Univ Valencia, Univ Clin Hosp, INCLIVA, Dept Nephrol, Av Blasco Ibanez 17, Valencia 46010, Spain

Torra, R:
 Univ Autonoma Barcelona, REDinREN, Nstituto Invest Carlos III,Inst Invest Biomed St, Fundacio Puigvert,Med Dept,Nephrol Dept,Inherited, Barcelona, Spain

Tomas, P:
 Univ Valencia, Univ Clin Hosp, INCLIVA, Dept Nephrol, Av Blasco Ibanez 17, Valencia 46010, Spain

Puchades, MJ:
 Univ Valencia, Univ Clin Hosp, INCLIVA, Dept Nephrol, Av Blasco Ibanez 17, Valencia 46010, Spain

Panizo, N:
 Univ Valencia, Univ Clin Hosp, INCLIVA, Dept Nephrol, Av Blasco Ibanez 17, Valencia 46010, Spain

Pantoja, J:
 Univ Dr Peset Hosp, Dept Nephrol, Valencia, Spain

Montomoli, M:
 Univ Valencia, Univ Clin Hosp, INCLIVA, Dept Nephrol, Av Blasco Ibanez 17, Valencia 46010, Spain

Llisterri, JL:
 Clin Vallada, Calle San Ramon 2, Valencia 46691, Spain

Pallares-Carratala, V:
 Jaume I Univ, Castellon Mutual Insurance Union, Hlth Surveillance Unit, Dept Med, Castellon de La Plana, Spain

Valdivielso, JM:
 Univ Lleida, Stat Dept 2, Vasc & Renal Translat Res Grp, UDETMA,REDinREN ISCIII,IRBLleida, Lleida, Spain
ISSN: 14712369





BMC Nephrology
Editorial
BMC, CAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 22 Número: 1
Páginas:
WOS Id: 000635204400003
ID de PubMed: 33765945
imagen Green Published, gold

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