Distribution of asymmetric dimethylarginine among 980 healthy, older adults of different ethnicities

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Distribution of asymmetric dimethylarginine among 980 healthy, older adults of different ethnicities. / Sydow, Karsten; Fortmann, Stephen P; Fair, Joan M; Varady, Ann; Hlatky, Mark A; Go, Alan S; Iribarren, Carlos; Tsao, Philip S; ADVANCE Investigators.

In: CLIN CHEM, Vol. 56, No. 1, 01.2010, p. 111-120.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Sydow, K, Fortmann, SP, Fair, JM, Varady, A, Hlatky, MA, Go, AS, Iribarren, C, Tsao, PS & ADVANCE Investigators 2010, 'Distribution of asymmetric dimethylarginine among 980 healthy, older adults of different ethnicities', CLIN CHEM, vol. 56, no. 1, pp. 111-120. https://doi.org/10.1373/clinchem.2009.136200

APA

Sydow, K., Fortmann, S. P., Fair, J. M., Varady, A., Hlatky, M. A., Go, A. S., Iribarren, C., Tsao, P. S., & ADVANCE Investigators (2010). Distribution of asymmetric dimethylarginine among 980 healthy, older adults of different ethnicities. CLIN CHEM, 56(1), 111-120. https://doi.org/10.1373/clinchem.2009.136200

Vancouver

Bibtex

@article{5809e4b41dad4a60a9bcb7e9dddf4779,
title = "Distribution of asymmetric dimethylarginine among 980 healthy, older adults of different ethnicities",
abstract = "BACKGROUND: Endothelium-derived nitric oxide plays a crucial role in the regulation of vascular tone and the development of cardiovascular disease. The endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA) has emerged as a novel cardiovascular risk factor. ADMA appears to be an independent predictor for cardiovascular and overall mortality. However, the majority of studies investigating the clinical role of ADMA were performed in European study populations with few individuals of other ethnicities.METHODS: We performed a cross-sectional study of 980 healthy, older (age 60-72 years) individuals of different ethnicities living in the San Francisco Bay area and analyzed ADMA plasma concentrations and their relationship to other cardiovascular risk factors. Plasma ADMA concentrations were measured using a recently developed, highly sensitive ELISA.RESULTS: In our entire sample, we were able to define a reference interval for ADMA plasma concentrations of 0.47 (90% CI 0.46-0.48) mumol/L to 0.85 (0.84-0.89) mumol/L. The mean ADMA concentration was 0.63 (SD 0.11) mumol/L (median 0.61 mumol/L). Mean ADMA concentrations were significantly lower in African Americans (0.60 mumol/L; P < 0.01) and mixed non-Hispanics (0.60 mumol/L; P < 0.05) compared with whites (0.63 mumol/L). ADMA was positively correlated with cystatin-C in both men (rho = 0.29) and women (rho = 0.37), and median plasma ADMA concentrations increased across cystatin-C quintiles.CONCLUSIONS: ADMA varies nearly 2-fold across a healthy sample of older men and women, correlates with age, body mass index, and renal function, and is different across ethnic groups. Additional studies in a wider age range and including larger ethnic subgroups would be useful.",
keywords = "African Continental Ancestry Group, Aged, Arginine/analogs & derivatives, Asian Continental Ancestry Group, Cardiovascular Diseases/etiology, Cystatin C/blood, Enzyme-Linked Immunosorbent Assay, European Continental Ancestry Group, Female, Glomerular Filtration Rate, Hispanic Americans, Humans, Male, Middle Aged, Regression Analysis, Risk Factors",
author = "Karsten Sydow and Fortmann, {Stephen P} and Fair, {Joan M} and Ann Varady and Hlatky, {Mark A} and Go, {Alan S} and Carlos Iribarren and Tsao, {Philip S} and {ADVANCE Investigators}",
year = "2010",
month = jan,
doi = "10.1373/clinchem.2009.136200",
language = "English",
volume = "56",
pages = "111--120",
journal = "CLIN CHEM",
issn = "0009-9147",
publisher = "American Association for Clinical Chemistry Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Distribution of asymmetric dimethylarginine among 980 healthy, older adults of different ethnicities

AU - Sydow, Karsten

AU - Fortmann, Stephen P

AU - Fair, Joan M

AU - Varady, Ann

AU - Hlatky, Mark A

AU - Go, Alan S

AU - Iribarren, Carlos

AU - Tsao, Philip S

AU - ADVANCE Investigators

PY - 2010/1

Y1 - 2010/1

N2 - BACKGROUND: Endothelium-derived nitric oxide plays a crucial role in the regulation of vascular tone and the development of cardiovascular disease. The endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA) has emerged as a novel cardiovascular risk factor. ADMA appears to be an independent predictor for cardiovascular and overall mortality. However, the majority of studies investigating the clinical role of ADMA were performed in European study populations with few individuals of other ethnicities.METHODS: We performed a cross-sectional study of 980 healthy, older (age 60-72 years) individuals of different ethnicities living in the San Francisco Bay area and analyzed ADMA plasma concentrations and their relationship to other cardiovascular risk factors. Plasma ADMA concentrations were measured using a recently developed, highly sensitive ELISA.RESULTS: In our entire sample, we were able to define a reference interval for ADMA plasma concentrations of 0.47 (90% CI 0.46-0.48) mumol/L to 0.85 (0.84-0.89) mumol/L. The mean ADMA concentration was 0.63 (SD 0.11) mumol/L (median 0.61 mumol/L). Mean ADMA concentrations were significantly lower in African Americans (0.60 mumol/L; P < 0.01) and mixed non-Hispanics (0.60 mumol/L; P < 0.05) compared with whites (0.63 mumol/L). ADMA was positively correlated with cystatin-C in both men (rho = 0.29) and women (rho = 0.37), and median plasma ADMA concentrations increased across cystatin-C quintiles.CONCLUSIONS: ADMA varies nearly 2-fold across a healthy sample of older men and women, correlates with age, body mass index, and renal function, and is different across ethnic groups. Additional studies in a wider age range and including larger ethnic subgroups would be useful.

AB - BACKGROUND: Endothelium-derived nitric oxide plays a crucial role in the regulation of vascular tone and the development of cardiovascular disease. The endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA) has emerged as a novel cardiovascular risk factor. ADMA appears to be an independent predictor for cardiovascular and overall mortality. However, the majority of studies investigating the clinical role of ADMA were performed in European study populations with few individuals of other ethnicities.METHODS: We performed a cross-sectional study of 980 healthy, older (age 60-72 years) individuals of different ethnicities living in the San Francisco Bay area and analyzed ADMA plasma concentrations and their relationship to other cardiovascular risk factors. Plasma ADMA concentrations were measured using a recently developed, highly sensitive ELISA.RESULTS: In our entire sample, we were able to define a reference interval for ADMA plasma concentrations of 0.47 (90% CI 0.46-0.48) mumol/L to 0.85 (0.84-0.89) mumol/L. The mean ADMA concentration was 0.63 (SD 0.11) mumol/L (median 0.61 mumol/L). Mean ADMA concentrations were significantly lower in African Americans (0.60 mumol/L; P < 0.01) and mixed non-Hispanics (0.60 mumol/L; P < 0.05) compared with whites (0.63 mumol/L). ADMA was positively correlated with cystatin-C in both men (rho = 0.29) and women (rho = 0.37), and median plasma ADMA concentrations increased across cystatin-C quintiles.CONCLUSIONS: ADMA varies nearly 2-fold across a healthy sample of older men and women, correlates with age, body mass index, and renal function, and is different across ethnic groups. Additional studies in a wider age range and including larger ethnic subgroups would be useful.

KW - African Continental Ancestry Group

KW - Aged

KW - Arginine/analogs & derivatives

KW - Asian Continental Ancestry Group

KW - Cardiovascular Diseases/etiology

KW - Cystatin C/blood

KW - Enzyme-Linked Immunosorbent Assay

KW - European Continental Ancestry Group

KW - Female

KW - Glomerular Filtration Rate

KW - Hispanic Americans

KW - Humans

KW - Male

KW - Middle Aged

KW - Regression Analysis

KW - Risk Factors

U2 - 10.1373/clinchem.2009.136200

DO - 10.1373/clinchem.2009.136200

M3 - SCORING: Journal article

C2 - 19892843

VL - 56

SP - 111

EP - 120

JO - CLIN CHEM

JF - CLIN CHEM

SN - 0009-9147

IS - 1

ER -