Table 1. Study Characteristicsa.
Source | Country | Study Duration | Total Participants Recruited, No./Total in Analysis, No. | Age, Mean (SD), y | Time Since Menopause, Mean (SD), y | HT | Amount of Physical Activity, Mean (SD) | ||
---|---|---|---|---|---|---|---|---|---|
Type | Dosage, mg/d | Follow-up Period/Duration of HT | |||||||
Aloia et al,60 1995 | United States | NA | 118/77 | 52.162 (5.7) | 2.27 (0.33) | E-P | E: 0.625 | E: 25 d/mo | None reported |
P: 10 | P: 9 d (days 16-25) | ||||||||
Bea et al,46 2011 | United States | 1993-2004 | 1)a 927/927 | 1) 63.35 (7.6) | 1) 22.21 (8.4) | 1) E | 0.625 | 7.7 (1.8) y | E: 10.1 (12.8)b |
Control: 9.3 (11.4)c | |||||||||
2) 1014/1014 | 2) 63.29 (7.2) | 2) 13.53 (8.5) | 2) E-P | E: 0.625 | 6.3 (1.5) y | E: 11.4 (14.6) | |||
P: 2.5 | Control: 11.9 (14.6) | ||||||||
Blackman et al,47 2002 | United States | 1992-1998 | 28/28 | 71.5 (5.9) | NA | E-P | E: 100 for 6 mo | E: 6 mo | None reported |
P: 10 for the last 10 d of each 28-d cycle | P: last 10 d of each 28-d cycle for 6 mo (approximately 60-65 d) | ||||||||
Chen et al,57 2005 | United States | 1993-2001 | 835/835; Sensitivity analysis: 511/256 (placebo arm), 511/255 (treatment arm) | 63.1 (7.2) | 13.8 (8.9) | E-P | E: 0.625 | 3 y | None reported |
P: 2.5 | |||||||||
Evans et al,61 2001 | United States | NA | 68/68 (But only 34 in HT and placebo groups combined) | 67.7 (5.2) | Mean (SD) age at menopause: 49 (5) y; current mean (SD) age: 67.8 (5) y | E-P | E: 0.625 | 13 d every third month | None reported |
P: 5 | |||||||||
Haarbo et al,48 1991 | Denmark | NA | 75/62 (19 HT) | 45-55 | 20.9 (8.4) mo | 1) E-P | E: 2 | 2 y | None reported |
P: 1 | |||||||||
75/62 (19 HT) | 22.4 (9.9) mo | 2) E-P | E: 2 | 2 y | |||||
P: 75 | |||||||||
Hassager and Christiansen,58 1989 | Denmark | 1983-1985 | 133/65 | 1) 49.91 (2.36) | Inclusion criteria: menopause within the past 0.5-3.0 | 1) E-P (oral) | E: 2 | In a 28-d cycle: E: days 1-11 | None reported |
P: | E-P: days 12-21 | ||||||||
None: days 22-28 | |||||||||
133/45 | 2) 50.41 (2.29) | 2) E (percutaneous) | E: 0.6 | In a 28-d cycle: | |||||
E: days 1-24, 5 g | |||||||||
None: days 25-28 | |||||||||
Jensen et al,49 2003d | Denmark | 1990-1993 | 1006/621 | 50.1 ( 2.8) | 0.7 (0.6) y | 1) E | 2 | 5 y | E: 0.98 (13.02)e |
2) E-P | E: 2 | In a 28 d cycle: | |||||||
P: 1 | E: days 1-12 | Control: 1.187 (12.66) | |||||||
E-P: days 13-22 E: days 23-28 | |||||||||
Kenny et al,50 2005 | United States | NA | 167/107 | 74.3 (6.2) | Mean (SD) age: 74.3 (0.6) | E | 0.25 (Ultralow dose) | 36 mo | E: Baseline: 120.9 (6.2)f |
36 mo: 104.8 (6.6) | |||||||||
Placebo: baseline: 99.8 (6.1) | |||||||||
36 mo: 84.7 (6.9) | |||||||||
Pöllänen et al,51 2007 | Finland | NA | 20/15 | 53.6 (1.85) | 2.8 (3.6) | E-P | E: 2 | 1 y | None reported |
P: 1 | |||||||||
Sipilä et al,52 2001 | Finland | NA | 80/52 (30 in HT and placebo groups combined) | 50-55 | Inclusion criteria: menopause within the past 5 y | E-P | E: 2 | 1 y | None reported |
P: 1 | |||||||||
Sørensen et al,59 2001 | Denmark | NA | 16/14 | 55.5 (2.6) | 5.9 (3.9) | E-P | E: 4 | In a 28-d cycle; follow-up/duration not specified | None reported |
P: 1 | E: 4 mg for 22 d and 1 mg for 6 d; P: 10 d; total: 12 wk | ||||||||
Thorneycroft et al,53 2007 | United States | NA | 822/502 | 51.9 (3.3) | 2.2 (0.9) | 1) E | 1A) E: 0.625 | 2 y | None reported |
51.5 (4.1) | 2.2 (0.9) | 1B) E: 0.45 | 2 y | ||||||
52.0 (3.7) | 2.5 (1.0) | 1C) E: 0.3 | 2 y | ||||||
51.5 (3.8) | 2.5 (0.9) | 2) E-P | 1A) E: 0.625 | 2 y | |||||
P: 2.5 | |||||||||
51.1 (3.5) | 2.3 (0.9) | 1B) E: 0.45 | 2 y | ||||||
P: 2.5 | |||||||||
52.3 (3.9) | 2.3 (1.0) | 1C) E: 0.45 | 2 y | ||||||
P: 1.5 | |||||||||
51.3 (3.5) | 2.3 (1.0) | 1D) E: 0.3 | 2 y | ||||||
P: 1.5 |
Abbreviations: E, estrogen therapy; E-P, estrogen plus progesterone therapy; HT, hormone therapy; NA, not available or not reported; P, progesterone therapy; SE, standard error.
Numbering refers to treatment group.
Mean (SD) of baseline weekly energy expenditure (metabolic equivalent values).
Control groups may have included women receiving placebo or women not receiving HT at all.
For the meta-analysis, both treatment arms from Jensen et al49 have been combined. The study did not provide separate lean body mass measures for treatment arms 1 and 2.
Mean (SD) of change in amount of exercise (hours per week) across course of study.
Mean (SE) of total baseline Physical Activity Scale for the Elderly (PASE) score. The PASE is a 5-minute, easily scored survey designed specifically to assess physical activity in epidemiological studies of persons aged 65 years and older. It is self-rated, scores range from 0 to 793, and higher scores indicate greater physical activity.72