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. Author manuscript; available in PMC: 2013 Sep 11.
Published in final edited form as: Menopause. 2010 Sep-Oct;17(5):946–954. doi: 10.1097/gme.0b013e3181d76953

Table 2.

Risk of Incident Symptoms1 at Year 1 by Prevalence of Symptoms2 at Baseline: WHI CEE trial (N = 10739)

Baseline Symptom Prevalence CEE Year 1 %3 (n4) Placebo Year 1 % (n) Risk Ratio (95% CI)5 P6 P-int7

Hot Flashes
 Not present 1.8 (4176) 4.3 (4269) 0.43 (0.33, 0.56) <0.001 0.26
 Present 20.2 (583) 39.3 (590) 0.51 (0.43, 0.62)

Night Sweats
 Not Present 3.9 (4136) 6.4 (4232) 0.61 (0.51, 0.74) <0.001 0.83
 Present 24.9 (595) 39.5 (598) 0.63 (0.53, 0.75)

Breast Tenderness
 Not Present 8.4 (4597) 3.4 (4708) 2.48 (2.08, 2.97) <0.001 <0.001
 Present 35.0 (160) 32.9 (155) 1.06 (0.78, 1.45)

Vaginal Dryness
 Not Present 4.1 (4227) 5.2 (4298) 0.79 (0.65, 0.96) <0.001 0.92
 Present 34.3 (499) 42.9 (522) 0.80 (0.68, 0.93)

Joint Pain
 Not Present 16.2 (3261) 17.9 (3333) 0.91 (0.81, 1.01) 0.04 0.20
 Present 66.1 (1467) 67.6 (1520) 0.98 (0.93, 1.03)

Mood Swings
 Not Present 5.4 (4349) 5.3 (4513) 1.02 (0.86, 1.22) 0.45 0.80
 Present 41.6 (377) 42.2 (344) 0.99 (0.83, 1.17)
1

Incidence of moderate or severe symptoms.

2

Presence of moderate or severe symptoms reported at baseline.

3

Proportion of N reporting symptoms at Year 1.

4

Number of participants in CEE or placebo with or without baseline symptom; denominator of (3).

5

Relative risk (95% confidence interval) of symptoms at Year 1 of CEE compared to placebo.

6

Test of main effect; corresponds to whether RR of CEE compared to placebo differs from unity regardless of presence or absence of baseline symptoms.

7

Test of interaction; corresponds to whether RR of CEE compared to placebo differs by presence or absence of baseline symptom.