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Table 2 Factors associated with risk of hypertension in adults 18–70 years

From: Impact of the common MTHFR 677C→T polymorphism on blood pressure in adulthood and role of riboflavin in modifying the genetic risk of hypertension: evidence from the JINGO project

 

All (n = 2566)

On antihypertensive drugs (n = 1255)

Not on antihypertensive drugs (n = 1311)

OR

95% CI

Pb

OR

95% CI

Pb

OR

95% CI

Pa

Age, years

1.04

1.03–1.05

< 0.001

1.01

0.98–1.04

0.568

1.05

1.03–1.06

< 0.001

Sex, male

1.86

1.50–2.32

< 0.001

1.69

1.28–2.25

0.001

1.77

1.23–2.56

0.002

BMI, kg/m2

1.06

1.04–1.08

< 0.001

1.03

1.01–1.05

0.009

1.11

1.07–1.15

< 0.001

Alcohol intake, units per week

1.01

1.00–1.02

0.005

1.01

1.00–1.02

0.325

1.03

1.01–1.04

< 0.001

Antihypertensive medication useb

2.01

1.60–2.52

< 0.001

      

Serum creatinine, μmol/L

1.00

0.99–1.00

0.307

1.00

0.99–1.00

0.189

1.01

0.99–1.02

0.340

Total cholesterol, mmol/L

1.26

1.15–1.38

< 0.001

1.25

1.11–1.41

< 0.001

1.23

1.07–1.41

0.004

Smoking

 Past

0.98

0.80–1.19

0.826

0.97

0.75–1.26

0.834

1.02

0.74–1.41

0.888

 Current

1.03

0.79–1.33

0.845

0.92

0.64–1.31

0.630

1.10

0.75–1.62

0.618

Study cohortc

1.79

1.29–2.48

< 0.001

2.40

1.40–4.11

< 0.001

2.09

1.31–3.32

0.002

Plasma homocysteine, μmol/L

1.00

0.98–1.02

0.958

0.98

0.96–1.00

0.074

1.06

1.02–1.10

0.002

MTHFR genotyped

 CT

1.18

0.98–1.43

0.082

1.35

1.05–1.73

0.018

0.98

0.73–1.32

0.889

 TT

1.42

1.07–1.90

0.016

1.40

0.95–2.06

0.093

1.37

0.88–2.11

0.161

  1. CI confidence interval, OR odds ratio
  2. aData analysed by logistic regression to predict hypertension as the categorical dependent variable; hypertension defined as systolic BP of ≥ 140 and/or a diastolic BP of ≥ 90 mmHg [1]
  3. bAs a binary (yes/no) covariate
  4. cComparing TUDA cohort with NANS cohort (reference category). See supplementary Table S1 for participant characteristics presented separately for each study cohort
  5. dCT (heterozygous) and TT (homozygous variant) genotypes for the MTHFR 677C→T polymorphism; reference category is the CC genotype