ホルモン療法は更年期女性の心臓の健康を改善できますか?(Can hormone therapy improve heart health in menopausal women?)

ad

2025-04-21 ペンシルベニア州立大学(PennState)

ペンシルベニア州立大学の研究によれば、エストロゲンを含む経口ホルモン療法は閉経後女性の心血管バイオマーカーを改善し、心疾患リスクの低減につながる可能性があることが示された。約2,700名の女性を対象に6年間追跡した結果、悪玉コレステロールの低下、善玉コレステロールの上昇、インスリン抵抗性の改善が確認された。また、遺伝的に高リスクとされるリポタンパク質(a)の濃度が最大20%減少した点は、特に注目される。この研究は閉経後10年以内の健康な女性に対するホルモン療法の安全性と有効性を支持している。

<関連情報>

女性健康イニシアチブホルモン療法臨床試験におけるホルモン療法後の心血管バイオマーカーの長期的変化 Long-Term Changes to Cardiovascular Biomarkers After Hormone Therapy in the Women’s Health Initiative Hormone Therapy Clinical Trials

Nudy, Matthew MD; Aragaki, Aaron K. MS; Jiang, Xuezhi MD, PhD; Manson, JoAnn E. MD, DrPH; Shadyab, Aladdin H. PhD; Jung, Su Yon PhD; Martin, Lisa W. MD; Wild, Robert A. MD, PhD; Womack, Catherine MD; Mouton, Charles P. MD, MBA; Rossouw, Jacques E. MD; Schnatz, Peter F. DO, MBA
Obstetrics & Gynecology  Published:April 2025
DOI:10.1097/AOG.0000000000005862

Abstract

OBJECTIVE:

To assess the long-term changes in cardiovascular biomarkers during the WHI (Women’s Health Initiative) hormone therapy (HT) clinical trials of conjugated equine estrogens (CEE) alone and CEE plus medroxyprogesterone acetate (MPA).

METHODS:

HT trial participants from the CEE alone (n=1,188, 0.625 mg/d CEE or placebo) and the CEE+MPA (n=1,508, 0.625 mg/d CEE plus continuous 2.5 mg/d MPA or placebo) trials provided blood samples at baseline and after 1, 3, and 6 years. Low-density lipoprotein cholesterol (LDL-C; primary endpoint), high-density lipoprotein cholesterol (HDL-C), triglycerides, total cholesterol, lipoprotein(a), glucose, insulin, and homeostatic model assessment for insulin resistance were measured. Repeated-measures regression models estimated the geometric means of each log-transformed biomarker by restricted maximum likelihood. A constant treatment effect across visits was used to estimate the overall effect, expressed as a ratio of geometric means, and was complemented with geometric means (95% CIs) by randomization group and corresponding ratios of geometric means (95% CI; HT vs placebo) at each visit.

RESULTS:

During the intervention phase of the CEE-alone trial, randomization to CEE reduced LDL-C by 11% over 6 years (ratio of geometric means 0.89, 95% CI, 0.88–0.91, P<.001). The overall reduction in LDL-C was similar for CEE+MPA relative to placebo (ratio of geometric means 0.88, 95% CI, 0.86–0.89, P<.001). Relative to placebo, HDL-C and triglycerides were 13.0% and 7.0% higher with CEE and CEE+MPA, respectively. The homeostatic model assessment for insulin resistance decreased by 14.0% and 8.0% for CEE-alone and CEE+MPA trial participants, respectively. Relative to placebo, lipoprotein(a) decreased by 15.0% and 20.0% for participants randomized to CEE alone and CEE+MPA, respectively.

CONCLUSION:

Lipoprotein(a), LDL-C, and homeostatic model assessment for insulin resistance were lower and HDL-C levels were higher for HT compared with placebo. Triglycerides increased in both the CEE and CEE+MPA trials, however. Future research should assess whether other progestogens attenuate the effect of estrogen on HDL-C. These results may be used to counsel younger menopausal women with bothersome symptoms who are deciding whether to initiate oral HT within the context of published effects of oral HT on rates of cardiovascular events.

CLINICAL TRIAL REGISTRATION:

ClinicalTrials.gov, NCT00000611.

医療・健康
ad
ad
Follow
ad
タイトルとURLをコピーしました