Aromatase Inhibitors and Plasma Lipid Changes in Postmenopausal Women with Breast Cancer: A Systematic Review and Meta-Analysis

被引:2
作者
Berczi, Balint [1 ]
Farkas, Nelli [2 ,3 ]
Hegyi, Peter [2 ,4 ]
Toth, Barbara [5 ,6 ]
Csupor, Dezso [2 ,5 ,6 ]
Nemeth, Balazs [1 ]
Lukacs, Anita [7 ]
Czumbel, Laszlo Mark [8 ]
Keremi, Beata [8 ]
Kiss, Istvan [1 ]
Szabo, Andrea [7 ]
Varga, Gabor [8 ]
Gerber, Gabor [9 ]
Gyongyi, Zoltan [1 ]
机构
[1] Univ Pecs, Med Sch, Dept Publ Hlth Med, Szigeti Ut 12, H-7624 Pecs, Hungary
[2] Univ Pecs, Inst Translat Med, Med Sch, Szigeti Ut 12, H-7624 Pecs, Hungary
[3] Univ Pecs, Inst Bioanal, Med Sch, Szigeti Ut 12, H-7624 Pecs, Hungary
[4] Univ Szeged, Dept Med 1, Koranyi Fasor 8-10, H-6720 Szeged, Hungary
[5] Univ Szeged, Dept Pharmacognosy, Eotvos U 6, H-6720 Szeged, Hungary
[6] Univ Szeged, Interdisciplinary Ctr Nat Prod, Dugonics Ter 13, H-6720 Szeged, Hungary
[7] Univ Szeged, Fac Med, Dept Publ Hlth, Dom Ter 10, H-6720 Szeged, Hungary
[8] Semmelweis Univ, Fac Dent, Dept Oral Biol, Nagyvarad Ter 4, H-1089 Budapest, Hungary
[9] Semmelweis Univ, Fac Med, Dept Anat Histol & Embryol, Tuzolto U 58, H-1094 Budapest, Hungary
关键词
breast cancer; lipids; anastrozole; exemestane; letrozole; meta-analysis; CARDIOVASCULAR EVENTS; ESTROGEN-RECEPTOR; ENDOCRINE THERAPY; DOUBLE-BLIND; EXEMESTANE; TAMOXIFEN; PROFILE; RISK; CHOLESTEROL; ANASTROZOLE;
D O I
10.3390/jcm13061818
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Women are typically diagnosed with estrogen receptor-positive breast cancer around the postmenopausal period when declining estrogen levels initiate changes in lipid profiles. Aromatase inhibitors (AI) are used to prevent the progression of cancer; however, a further reduction in estrogen levels may have detrimental effects on lipid levels, which was our working hypothesis. Methods: Our meta-analysis was conducted on the lipid profiles of postmenopausal breast cancer patients at baseline and at different treatment time points. Results: We identified 15 studies, including 1708 patients. Studies using anastrozole (ANA), exemestane (EXE), letrozole (LET), and tamoxifen (TMX) were involved. Subgroup analyses revealed that 3- and 12-month administrations of LET and EXE lead to negative changes in lipid profiles that tend to alter the lipid profile undesirably, unlike ANA and TMX. Conclusions: Our results suggest that, despite statistically significant results, EXE and LET may not be sufficient to cause severe dyslipidemia in patients without cardiovascular comorbidities according to the AHA/ACC Guideline on the Management of Blood Cholesterol. However, the results may raise the question of monitoring the effects of AIs in patients, especially those with pre-existing cardiovascular risk factors such as dyslipidemia.
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页数:20
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