Abstract
Original language | English |
---|---|
Pages (from-to) | 4324-4333 |
Number of pages | 10 |
Journal | Journal of Clinical Endocrinology & Metabolism |
Volume | 94 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2009 |
Keywords
- aldosterone
- aldosterone synthase
- antihypertensive agent
- beta adrenergic receptor blocking agent
- calcium antagonist
- dipeptidyl carboxypeptidase inhibitor
- diuretic agent
- marker
- potassium
- renin
- steroid 11beta monooxygenase
- adult
- aldosterone blood level
- article
- blood pressure
- blood pressure monitoring
- body mass
- Caucasian
- chemoluminescence
- environmental factor
- family
- female
- gene locus
- genetic association
- genetic variability
- heredity
- heritability
- homeostasis
- human
- hypertension
- immunoassay
- intron
- major clinical study
- male
- phenotype
- plasma renin activity
- population
- priority journal
- single nucleotide polymorphism
- Adult
- Aldosterone
- Blood Pressure
- Body Mass Index
- Circadian Rhythm
- European Continental Ancestry Group
- Family
- Female
- Genotype
- Humans
- Hypertension
- Male
- Middle Aged
- Phenotype
- Renin
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In: Journal of Clinical Endocrinology & Metabolism, Vol. 94, No. 11, 2009, p. 4324-4333.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Familial and phenotypic associations of the aldosterone renin ratio
AU - Alvarez-Madrazo, S.
AU - Padmanabhan, S.
AU - Mayosi, B.M.
AU - Watkins, H.
AU - Avery, P.
AU - Wallace, A.M.
AU - Fraser, R.
AU - Davies, E.
AU - Keavney, B.
AU - Connell, J. M.
N1 - Cited By (since 1996): 10 Export Date: 19 March 2012 Source: Scopus CODEN: JCEMA doi: 10.1210/jc.2009-1406 PubMed ID: 19820005 Language of Original Document: English Correspondence Address: Keavney, B.; Department of Cardiovascular Sciences, University of Newcastle, Newcastle upon Tyne NE1 3BZ, United Kingdom; email: [email protected] Chemicals/CAS: aldosterone, 52-39-1, 6251-69-0; aldosterone synthase, 122933-89-5; potassium, 7440-09-7; renin, 61506-93-2, 9015-94-5; steroid 11beta monooxygenase, 9029-66-7, 9054-99-3; Aldosterone, 52-39-1; Renin, 3.4.23.15 References: Montori, V.M., Young Jr., W.F., Use of plasma aldosterone concentration-to-plasma renin activity ratio as a screening test for primary aldosteronism. A systematic review of the literature (2002) Endocrinol Metab Clin North Am, 31, pp. 619-632. , xi; Mulatero, P., Stowasser, M., Loh, K.-C., Fardella, C.E., Gordon, R.D., Mosso, L., Gomez-Sanchez, C.E., Young Jr., W.F., Increased diagnosis of primary aldosteronism, including surgically correctable forms, in centers from five continents (2004) Journal of Clinical Endocrinology and Metabolism, 89 (3), pp. 1045-1050. , DOI 10.1210/jc.2003-031337; Funder, J.W., Carey, R.M., Fardella, C., Gomez-Sanchez, C.E., Mantero, F., Stowasser, M., Young Jr., W.F., Montori, V.M., Case detection, diagnosis, and treatment of patients with primary aldosteronism: An Endocrine Society Clinical Practice Guideline (2008) J Clin Endocrinol Metab, 93, pp. 3266-3281; Padfield, P.L., Prevalence and role of a raised aldosterone to renin ratio in the diagnosis of primary aldosteronism: A debate on the scientific logic of the use of the ratio in practice (2003) Clin Endocrinol, 59, pp. 422-426. , Oxf; Douma, S., Petidis, K., Doumas, M., Papaefthimiou, P., Triantafyllou, A., Kartali, N., Papadopoulos, N., Zamboulis, C., Prevalence of primary hyperaldosteronism in resistant hypertension: A retrospective observational study (2008) The Lancet, 371 (9628), pp. 1921-1926. , DOI 10.1016/S0140-6736(08)60834-X, PII S014067360860834X; Gordon, R.D., Ziesak, M.D., Tunny, T.J., Stowasser, M., Klemm, S.A., Evidence that primary aldosteronism may not be uncommon: 12% incidence among antihypertensive drug trial volunteers (1993) Clinical and Experimental Pharmacology and Physiology, 20 (5), pp. 296-298; Lim, P.O., Rodgers, P., Cardale, K., Watson, A.D., MacDonald, T.M., Potentially high prevalence of primary aldosteronism in a primary-care population (1999) Lancet, 353 (9146), p. 40; Stowasser, M., Gordon, R.D., Primary aldosteronism - Careful investigation is essential and rewarding (2004) Molecular and Cellular Endocrinology, 217 (1-2), pp. 33-39. , DOI 10.1016/j.mce.2003.10.006, PII S0303720703003770; Padfield, P.L., Primary aldosteronism, a common entity? The myth persists (2002) J Hum Hypertens, 16, pp. 159-162; Rossi, G.P., Bernini, G., Caliumi, C., Desideri, G., Fabris, B., Ferri, C., Ganzaroli, C., Mantero, F., A Prospective Study of the Prevalence of Primary Aldosteronism in 1,125 Hypertensive Patients (2006) Journal of the American College of Cardiology, 48 (11), pp. 2293-2300. , DOI 10.1016/j.jacc.2006.07.059, PII S0735109706023321; Connell, J.M., MacKenzie, S.M., Freel, E.M., Fraser, R., Davies, E., A lifetime of aldosterone excess: Long-term consequences of altered regulation of aldosterone production for cardiovascular function (2008) Endocr Rev, 29, pp. 133-154; Connell, J.M., Davies, E., The new biology of aldosterone (2005) J Endocrinol, 186, pp. 1-20; Alderman, M.H., Cohen, H.W., Sealey, J.E., Laragh, J.H., Plasma renin activity levels in hypertensive persons: Their wide range and lack of suppression in diabetic and in most elderly patients (2004) Am J Hypertens, 17, pp. 1-7; Goodfriend, T.L., Calhoun, D.A., Resistant Hypertension, Obesity, Sleep Apnea, and Aldosterone: Theory and Therapy (2004) Hypertension, 43 (3), pp. 518-524. , DOI 10.1161/01.HYP.0000116223.97436.e5; Tiu, S.C., Choi, C.H., Shek, C.C., Ng, Y.W., Chan, F.K., Ng, C.M., Kong, A.P., The use of aldosterone-renin ratio as a diagnostic test for primary hyperaldosteronism and its test characteristics under different conditions of blood sampling (2005) J Clin Endocrinol Metab, 90, pp. 72-78; James, G.D., Sealey, J.E., Muller, F., Renin relationship to sex, race and age in a normotensive population (1986) Journal of Hypertension, 4 (SUPPL. 5), pp. S387-S389; Schunkert, H., Jan Danser, A.H., Hense, H.-W., Derkx, F.H.M., Kurzinger, S., Riegger, G.A.J., Effects of estrogen replacement therapy on the renin-angiotensin system in postmenopausal women (1997) Circulation, 95 (1), pp. 39-45; Vasan, R.S., Evans, J.C., Larson, M.G., Wilson, P.W.F., Meigs, J.B., Rifai, N., Benjamin, E.J., Levy, D., Serum aldosterone and the incidence of hypertension in nonhypertensive persons (2004) New England Journal of Medicine, 351 (1), pp. 33-41+111. , DOI 10.1056/NEJMoa033263; Newton-Cheh, C., Guo, C.-Y., Gona, P., Larson, M.G., Benjamin, E.J., Wang, T.J., Kathiresan, S., Vasan, R.S., Clinical and genetic correlates of aldosterone-to-renin ratio and relations to blood pressure in a community sample (2007) Hypertension, 49 (4), pp. 846-856. , DOI 10.1161/01.HYP.0000258554.87444.91; Parikh, N.I., Gona, P., Larson, M.G., Wang, T.J., Newton-Cheh, C., Levy, D., Benjamin, E.J., Vasan, R.S., Plasma renin and risk of cardiovascular disease and mortality: The Framingham Heart Study (2007) European Heart Journal, 28 (21), pp. 2644-2652. , DOI 10.1093/eurheartj/ehm399; Davies, E., Holloway, C.D., Ingram, M.C., Inglis, G.C., Friel, E.C., Morrison, C., Anderson, N.H., Connell, J.M.C., Aldosterone excretion rate and blood pressure in essential hypertension are related to polymorphic differences in the aldosterone synthase gene CYP11B2 (1999) Hypertension, 33 (2), pp. 703-707; Baker, M., Gaukrodger, N., Mayosi, B.M., Imrie, H., Farrall, M., Watkins, H., Connell, J.M.C., Keavney, B., Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: A family study (2005) Diabetes, 54 (8), pp. 2492-2496. , DOI 10.2337/diabetes.54.8.2492; Gaukrodger, N., Mayosi, B.M., Imrie, H., Avery, P., Baker, M., Connell, J.M.C., Watkins, H., Keavney, B., A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: A study of 1428 individuals in 248 families (2005) Journal of Medical Genetics, 42 (6), pp. 474-478. , DOI 10.1136/jmg.2004.027631; Keavney, B., Mayosi, B., Gaukrodger, N., Imrie, H., Baker, M., Fraser, R., Ingram, M., Connell, J., Genetic variation at the locus encompassing 11-ß hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion (2005) Journal of Clinical Endocrinology and Metabolism, 90 (2), pp. 1072-1077. , DOI 10.1210/jc.2004-0870; Barr, M., MacKenzie, S.M., Friel, E.C., Holloway, C.D., Wilkinson, D.M., Brain, N.J.R., Ingram, M.C., Davies, E., Polymorphic variation in the 11ß-hydroxylase gene associates with reduced 11-hydroxylase efficiency (2007) Hypertension, 49 (1), pp. 113-119. , DOI 10.1161/01.HYP.0000249904.93940.7a, PII 0000426820070100000024; Imrie, H., Freel, M., Mayosi, B.M., Davies, E., Fraser, R., Ingram, M., Cordell, H.J., Connell, J.M.C., Association between aldosterone production and variation in the 11ß-hydroxylase (CYP11B1) gene (2006) Journal of Clinical Endocrinology and Metabolism, 91 (12), pp. 5051-5056. , http://jcem.endojournals.org/cgi/reprint/91/12/5051, DOI 10.1210/jc.2006-1481; Newton-Cheh, C., Johnson, T., Gateva, V., Tobin, M.D., Bochud, M., Coin, L., Najjar, S., Newhouse, S.J., Genome-wide association study identifies eight loci associated with blood pressure (2009) Nat Genet, 41, pp. 666-676; Tobin, M.D., Sheehan, N.A., Scurrah, K.J., Burton, P.R., Adjusting for treatment effects in studies of quantitative traits: Antihypertensive therapy and systolic blood pressure (2005) Stat Med, 24, pp. 2911-2935; Abecasis, G.R., Cherny, S.S., Cookson, W.O., Cardon, L.R., Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees (2002) Nat Genet, 30, pp. 97-101; Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M.A.R., Bender, D., Maller, J., Sham, P.C., PLINK: A tool set for whole-genome association and population-based linkage analyses (2007) American Journal of Human Genetics, 81 (3), pp. 559-575. , DOI 10.1086/519795; Gordon, R.D., Stowasser, M., Tunny, T.J., Klemm, S.A., Rutherford, J.C., High incidence of primary aldosteronism in 199 patients referred with hypertension (1994) Clinical and Experimental Pharmacology and Physiology, 21 (4), pp. 315-318; Mulatero, P., Rabbia, F., Milan, A., Paglieri, C., Morello, F., Chiandussi, L., Veglio, F., Drug effects on aldosterone/plasma renin activity ratio in primary aldosteronism (2002) Hypertension, 40 (6), pp. 897-902. , DOI 10.1161/01.HYP.0000038478.59760.41; Sealey, J.E., Itskovitz-Eldor, J., Rubattu, S., James, G.D., August, P., Thaler, I., Levron, J., Laragh, J.H., Estradiol- And progesterone-related increases in the renin-aldosterone system: Studies during ovarian stimulation and early pregnancy (1994) Journal of Clinical Endocrinology and Metabolism, 79 (1), pp. 258-264. , DOI 10.1210/jc.79.1.258; Paillard, F., Chansel, D., Brand, E., Benetos, A., Thomas, F., Czekalski, S., Ardaillou, R., Soubrier, F., Genotype-phenotype relationships for the renin-angiotensin-aldosterone system in a normal population (1999) Hypertension, 34 (3), pp. 423-429; Connell, J.M., Fraser, R., MacKenzie, S., Davies, E., Is altered adrenal steroid synthesis a key intermediate phenotype in hypertension? (2003) Hypertension, 41, pp. 993-999
PY - 2009
Y1 - 2009
N2 - Context: The aldosterone to renin ratio (ARR) is a marker of aldosterone excess, widely used to screen for primary aldosteronism (PA). The significance of a raised ARR in normotensive and hypertensive subjects and the phenotypic and familial factors affecting it are unclear. Objective: We estimated the distribution and heritability of the ARR and tested for associations between ARR and blood pressure (BP) with 11 polymorphisms at the CYP11B1/CYP11B2 locus. Design and Setting: A total of 1172 individuals from 248 Caucasian families ascertained via a hypertensive proband were evaluated. Main Outcome Measure: Plasma aldosterone was measured by RIA, and plasma renin concentration was measured by the LIAISON Direct Renin chemiluminescent immunoassay. Results: Unadjusted and adjusted ARR were continuously distributed in normotensives and hypertensives, with no evidence of a cutoff that would identify a separate population with PA. Median ARR was 4.19 ng/liter per mIU/liter (range, 0.04-253.16). ARR levels were higher in females and associated with age, body mass index, and potassium. Antihypertensive agents had significant predictable effects on the ARR. Renin was negatively associated, and ARR was positively associated with ambulatory BP readings (P < 0.001) in subjects not taking antihypertensives. The heritability of the ARR was 38.1% (P < 10 -8). Plasma aldosterone, but not ARR, was influenced by the intron 2 conversion variation in the CYP11B2 gene (ß = -0.07; P = 0.04). Conclusions: The ARR is continuously distributed, is influenced by genetic and environmental factors, and is not a marker of a distinct pathological abnormality but possibly reflects the long-term influence of aldosterone on cardiovascular homeostasis. Copyright © 2009 by The Endocrine Society.
AB - Context: The aldosterone to renin ratio (ARR) is a marker of aldosterone excess, widely used to screen for primary aldosteronism (PA). The significance of a raised ARR in normotensive and hypertensive subjects and the phenotypic and familial factors affecting it are unclear. Objective: We estimated the distribution and heritability of the ARR and tested for associations between ARR and blood pressure (BP) with 11 polymorphisms at the CYP11B1/CYP11B2 locus. Design and Setting: A total of 1172 individuals from 248 Caucasian families ascertained via a hypertensive proband were evaluated. Main Outcome Measure: Plasma aldosterone was measured by RIA, and plasma renin concentration was measured by the LIAISON Direct Renin chemiluminescent immunoassay. Results: Unadjusted and adjusted ARR were continuously distributed in normotensives and hypertensives, with no evidence of a cutoff that would identify a separate population with PA. Median ARR was 4.19 ng/liter per mIU/liter (range, 0.04-253.16). ARR levels were higher in females and associated with age, body mass index, and potassium. Antihypertensive agents had significant predictable effects on the ARR. Renin was negatively associated, and ARR was positively associated with ambulatory BP readings (P < 0.001) in subjects not taking antihypertensives. The heritability of the ARR was 38.1% (P < 10 -8). Plasma aldosterone, but not ARR, was influenced by the intron 2 conversion variation in the CYP11B2 gene (ß = -0.07; P = 0.04). Conclusions: The ARR is continuously distributed, is influenced by genetic and environmental factors, and is not a marker of a distinct pathological abnormality but possibly reflects the long-term influence of aldosterone on cardiovascular homeostasis. Copyright © 2009 by The Endocrine Society.
KW - aldosterone
KW - aldosterone synthase
KW - antihypertensive agent
KW - beta adrenergic receptor blocking agent
KW - calcium antagonist
KW - dipeptidyl carboxypeptidase inhibitor
KW - diuretic agent
KW - marker
KW - potassium
KW - renin
KW - steroid 11beta monooxygenase
KW - adult
KW - aldosterone blood level
KW - article
KW - blood pressure
KW - blood pressure monitoring
KW - body mass
KW - Caucasian
KW - chemoluminescence
KW - environmental factor
KW - family
KW - female
KW - gene locus
KW - genetic association
KW - genetic variability
KW - heredity
KW - heritability
KW - homeostasis
KW - human
KW - hypertension
KW - immunoassay
KW - intron
KW - major clinical study
KW - male
KW - phenotype
KW - plasma renin activity
KW - population
KW - priority journal
KW - single nucleotide polymorphism
KW - Adult
KW - Aldosterone
KW - Blood Pressure
KW - Body Mass Index
KW - Circadian Rhythm
KW - European Continental Ancestry Group
KW - Family
KW - Female
KW - Genotype
KW - Humans
KW - Hypertension
KW - Male
KW - Middle Aged
KW - Phenotype
KW - Renin
UR - http://www.scopus.com/inward/record.url?scp=70449122766&partnerID=8YFLogxK
U2 - 10.1210/jc.2009-1406
DO - 10.1210/jc.2009-1406
M3 - Article
C2 - 19820005
SN - 0021-972X
VL - 94
SP - 4324
EP - 4333
JO - Journal of Clinical Endocrinology & Metabolism
JF - Journal of Clinical Endocrinology & Metabolism
IS - 11
ER -