American Indian chronic Renal insufficiency cohort study (AI-CRIC study).


Journal

BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793

Informations de publication

Date de publication:
22 07 2020
Historique:
received: 16 04 2020
accepted: 15 07 2020
entrez: 24 7 2020
pubmed: 24 7 2020
medline: 14 10 2021
Statut: epublish

Résumé

Chronic kidney disease (CKD) is an increasing epidemic globally that is associated with adverse health outcomes including end stage kidney disease (ESKD), cardiovascular disease (CVD), and death. American Indians (AIs) have a higher prevalence of CKD than most other racial/ethnic groups, due in part to a high prevalence of type 2 diabetes. Other genetic and environmental factors not yet identified may also contribute to the disproportionate burden of CKD in AIs. We will establish 3 clinical centers to recruit AIs from the Southwest United States (US) to expand the Chronic Renal Insufficiency Cohort (CRIC) study. We will follow the current CRIC protocol for kidney and cardiovascular measures and outcomes, which include ambulatory monitoring of kidney function and the use of mobile health technologies for CVD sub-phenotyping, and compare the outcomes in AIs with those in other racial/ethnic groups in CRIC. AI-CRIC will identify the role of various risk factors for rapid loss of kidney function among AIs of the Southwest US. In addition, to better understand the natural history of CKD and CVD in this high-risk population, we will identify unique risk factors for CKD and CVD progression in AIs. We will also compare event rates and risk factors for kidney and cardiovascular events in AIs with the other populations represented in CRIC.

Sections du résumé

BACKGROUND
Chronic kidney disease (CKD) is an increasing epidemic globally that is associated with adverse health outcomes including end stage kidney disease (ESKD), cardiovascular disease (CVD), and death. American Indians (AIs) have a higher prevalence of CKD than most other racial/ethnic groups, due in part to a high prevalence of type 2 diabetes. Other genetic and environmental factors not yet identified may also contribute to the disproportionate burden of CKD in AIs.
METHOD
We will establish 3 clinical centers to recruit AIs from the Southwest United States (US) to expand the Chronic Renal Insufficiency Cohort (CRIC) study. We will follow the current CRIC protocol for kidney and cardiovascular measures and outcomes, which include ambulatory monitoring of kidney function and the use of mobile health technologies for CVD sub-phenotyping, and compare the outcomes in AIs with those in other racial/ethnic groups in CRIC.
DISCUSSION
AI-CRIC will identify the role of various risk factors for rapid loss of kidney function among AIs of the Southwest US. In addition, to better understand the natural history of CKD and CVD in this high-risk population, we will identify unique risk factors for CKD and CVD progression in AIs. We will also compare event rates and risk factors for kidney and cardiovascular events in AIs with the other populations represented in CRIC.

Identifiants

pubmed: 32698776
doi: 10.1186/s12882-020-01954-y
pii: 10.1186/s12882-020-01954-y
pmc: PMC7376925
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

291

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002548
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK060990
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK119199
Pays : United States
Organisme : NIH HHS
ID : 1R01DK11919901
Pays : United States
Organisme : NCRR NIH HHS
ID : P20 RR016480
Pays : United States

Investigateurs

Lawrence J Appel (LJ)
Alan S Go (AS)
Jiang He (J)
James P Lash (JP)
Mahboob Rahman (M)
Panduranga S Rao (PS)
Raymond R Townsend (RR)

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Auteurs

Mark L Unruh (ML)

Department of Internal Medicine and Biochemistry, University of New Mexico, School of Medicine, MSC 10 5550, Albuquerque, NM, 87131, USA.

Soraya Arzhan (S)

Department of Internal Medicine and Biochemistry, University of New Mexico, School of Medicine, MSC 10 5550, Albuquerque, NM, 87131, USA.

Harold I Feldman (HI)

University of Pennsylvania, Philadelphia, PA, USA.

Helen C Looker (HC)

NIDDK, NIH, Phoenix, AZ, USA.

Robert G Nelson (RG)

NIDDK, NIH, Phoenix, AZ, USA.

Thomas Faber (T)

Indian Health Services, Zuni, NM, USA.

David Johnson (D)

First Nations Hospital, Albuquerque, NM, USA.

Linda Son-Stone (L)

First Nations Hospital, Albuquerque, NM, USA.

Vernon S Pankratz (VS)

Department of Internal Medicine and Biochemistry, University of New Mexico, School of Medicine, MSC 10 5550, Albuquerque, NM, 87131, USA.

Larissa Myaskovsky (L)

Department of Internal Medicine and Biochemistry, University of New Mexico, School of Medicine, MSC 10 5550, Albuquerque, NM, 87131, USA.

Vallabh O Shah (VO)

Department of Internal Medicine and Biochemistry, University of New Mexico, School of Medicine, MSC 10 5550, Albuquerque, NM, 87131, USA. VShah@salud.unm.edu.

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