TY - JOUR
T1 - I/D polymorphism of the angiotensin-converting enzyme gene does not predict isolated systolic or systolic-diastolic hypertension in the elderly
AU - Johnson, A. G.
AU - Simons, L. A.
AU - Friedlander, Y.
AU - Simons, J.
AU - Davis, D. R.
AU - MaCallum, J.
PY - 1996/3
Y1 - 1996/3
N2 - To determine whether insertion/deletion (I/D) polymorphism (intron 16) of the angiotensin converting-enzyme (ACE) gene is associated with isolated systolic hypertension (ISH: systolic blood pressure (BP) ≥160, diastolic BP <90 mm Hg) or systolic-diastolic hypertension (S-D hypertension: diastolic BP ≥90 ± systolic BP ≥ 160 mm Hg) compared with normotensive controls (systolic BP <160, diastolic BP <90 mm Hg), we conducted a case-control study of 733 non-institutionalised, elderly (≥60 years) residents of Dubbo, NSW. Individuals were classified as: ISH (n = 167), S-D hypertension (n = 207) and normotensive control (n = 359) with age and sex matching. II, DD and ID genotypes were determined by a nested PCR strategy using DNA extracted from serum. The frequencies of D and I alleles in the control population (0.70 and 0.30 respectively) were not significantly different in the ISH group or the S-D hypertension group (χ2: 1.7, P = 0.42). After adjustment for several potential confounders, neither genotype nor allele predicted ISH (II vs DD: odds ratio (OR): 1.06, 95% confidence interval (CI): 0.55-2.03; I vs D: 1.09, 0.82-1.46) or S-D hypertension (II vs DD: 1.19, 0.67-2.10; I vs D: 1.16, 0.89-1.52) in this elderly cohort. The I/D polymorphism of the ACE gene is not a marker for either form of hypertension in this large elderly sample.
AB - To determine whether insertion/deletion (I/D) polymorphism (intron 16) of the angiotensin converting-enzyme (ACE) gene is associated with isolated systolic hypertension (ISH: systolic blood pressure (BP) ≥160, diastolic BP <90 mm Hg) or systolic-diastolic hypertension (S-D hypertension: diastolic BP ≥90 ± systolic BP ≥ 160 mm Hg) compared with normotensive controls (systolic BP <160, diastolic BP <90 mm Hg), we conducted a case-control study of 733 non-institutionalised, elderly (≥60 years) residents of Dubbo, NSW. Individuals were classified as: ISH (n = 167), S-D hypertension (n = 207) and normotensive control (n = 359) with age and sex matching. II, DD and ID genotypes were determined by a nested PCR strategy using DNA extracted from serum. The frequencies of D and I alleles in the control population (0.70 and 0.30 respectively) were not significantly different in the ISH group or the S-D hypertension group (χ2: 1.7, P = 0.42). After adjustment for several potential confounders, neither genotype nor allele predicted ISH (II vs DD: odds ratio (OR): 1.06, 95% confidence interval (CI): 0.55-2.03; I vs D: 1.09, 0.82-1.46) or S-D hypertension (II vs DD: 1.19, 0.67-2.10; I vs D: 1.16, 0.89-1.52) in this elderly cohort. The I/D polymorphism of the ACE gene is not a marker for either form of hypertension in this large elderly sample.
KW - Angiotensin converting enzyme gene
KW - Elderly
KW - Polymorphism
UR - http://www.scopus.com/inward/record.url?scp=0029961702&partnerID=8YFLogxK
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C2 - 8733034
AN - SCOPUS:0029961702
SN - 0950-9240
VL - 10
SP - 167
EP - 169
JO - Journal of Human Hypertension
JF - Journal of Human Hypertension
IS - 3
ER -