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Bioidentical Hormones - U.S. Senate Special Committee on Aging

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lood pressure in women taking CEE is<br />

<strong>on</strong>e possible c<strong>on</strong>tributor to this effect because<br />

relatively small differences in systolic<br />

blood pressure have been positively<br />

associated with differences in<br />

stroke and cardiovascular disease<br />

ratte.s.`<br />

The WHI esirogen-al<strong>on</strong>e trial provides<br />

str<strong>on</strong>g evidence that CEE reduces<br />

the nsk of hip, clinical vertebral, and<br />

other fractures. These reducti<strong>on</strong>s were<br />

of similar magnitude to those observed<br />

in the WHI estrogen plus progestin trial3'<br />

and are c<strong>on</strong>sistent with findings from<br />

prior observati<strong>on</strong>al studies 5 " 4 and recent<br />

meta-analyses.""<br />

177<br />

The tTend toward a reducti<strong>on</strong> in<br />

breast cancer incidence was unanticipated<br />

and is opposite of that observed<br />

in the WHI estrogen plus progestin trial,<br />

which reported a 24% increased risk.'o<br />

These results also appear c<strong>on</strong>trary to the<br />

prep<strong>on</strong>derance of observati<strong>on</strong>al study<br />

results,"' including those from the recent<br />

Milli<strong>on</strong> Women Study.' When examining<br />

breast cancer nsk by type of<br />

horm<strong>on</strong>e therapy, most of these studies<br />

have reported a modest increase in<br />

breast cancer risk with estrogen al<strong>on</strong>e<br />

but a greater risk for estrogen plus progestin.<br />

Still others have recently found<br />

little or no effect of estrogen al<strong>on</strong>e <strong>on</strong><br />

Figmno 5. Selected Clinical Otc<strong>on</strong>es by Participant Age and Randomiuati<strong>on</strong> Asrsgnment<br />

00. tby Aw. y<br />

cosraw ae<strong>on</strong> rieg<br />

7o 79<br />

toms<br />

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ve Thr-<br />

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70~. 8t C<br />

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70 79<br />

50-49<br />

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5000 070.9 0455<br />

70 ze<br />

tArsosen d S) H0rsa IPWU<br />

lasts co<br />

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Ji.<br />

C£E Pl..b.<br />

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05 555 0.330aos 3a 82Q .3a<br />

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3025.5D 5 s53250.555 o0 08-0 .50 1<br />

3 1250 32<br />

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2 400 ( 0527 0 597) 3 5<br />

2M0 e2~ e 1s 1 6 397-1.3't J<br />

.0o<br />

Fres s F a<br />

CEE I Rbo<br />

51<br />

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'5<br />

EFFECTS OF POSTMENOPAUSAL ESTROGEN<br />

breast cancer risk." Differences in<br />

breast cancer screening between the<br />

CEE and placebo groups do not explain<br />

the observed breast caticer effects<br />

because the WHI protocol mandated<br />

annual mammography and<br />

clinical breast examinati<strong>on</strong>s. The possibility<br />

that diagnostic delay could account<br />

for this reductiots seems remote<br />

because the effect of CEE al<strong>on</strong>e <strong>on</strong><br />

breast density is issnimal. L<strong>on</strong>gerterm<br />

effects ofCEE <strong>on</strong> breast cancer risk<br />

remain uncertain. Extended lollowup,<br />

as is currently planned, and analyses<br />

of breast cancer characteristics similar<br />

to those reported for the estrogets<br />

00 05 I0 5.5 20 2s 30 3s 40 s s5o ss e0<br />

HCrd eDte<br />

CEE mdic&te rpgatad eou.ne esto.g-; Ci, -6nd-nr ieW-W. Dat. - plotted as hurad rWio, -th e-n Dar showing 95% Cls.<br />

02004 Amn-c-r. Mcdsltdir. All rigisgh se-e-ed. (Repsstsdt) t4AM April 1t, 2004-V 3<br />

291, N5.. t1 1709<br />

-ownoa3dn fCrossa, 5 jar-iao -. at Ntiotnat InstietoCf Hith, <strong>on</strong> April 16, 2007

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