2014
DOI: 10.1016/j.yexcr.2014.07.002
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Ritonavir binds to and downregulates estrogen receptors: Molecular mechanism of promoting early atherosclerosis

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Cited by 10 publications
(7 citation statements)
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“…First, sex-based differences in immune activation have been described with a stronger interferon alpha response in women [ 27 ] possibly contributing to metabolic disorders. Second, HIV infection and antiretroviral treatments may interact with the estrogen/testosterone balance promoting androgen exposure, resulting in an increase of visceral abdominal fat and lipid concentrations [ 21 , 28 , 29 ], with more visible effects in women. Finally, differences in dietary and lifestyle habits such as alcohol consumption, physical activity and psychological status [ 21 ], might also explain an effect of gender on the associations between HIV and metabolic abnormalities.…”
Section: Discussionmentioning
confidence: 99%
“…First, sex-based differences in immune activation have been described with a stronger interferon alpha response in women [ 27 ] possibly contributing to metabolic disorders. Second, HIV infection and antiretroviral treatments may interact with the estrogen/testosterone balance promoting androgen exposure, resulting in an increase of visceral abdominal fat and lipid concentrations [ 21 , 28 , 29 ], with more visible effects in women. Finally, differences in dietary and lifestyle habits such as alcohol consumption, physical activity and psychological status [ 21 ], might also explain an effect of gender on the associations between HIV and metabolic abnormalities.…”
Section: Discussionmentioning
confidence: 99%
“…CircRNAs have been reported to play important roles in various diseases, such as atherosclerosis 77 , nervous system disorders 78 , diabetes 79 , and cancer 80 , 81 . The unique features and diverse functions of circRNAs make them promising candidates with clinical potentials in life sciences and medicine.…”
Section: Circrnas In Diagnosis and Prognosis Of Human Cancersmentioning
confidence: 99%
“…This statement is based upon the fact that interactions between pharmacokinetic boosters and exogenous estrogens exist [124] such that regimens requiring ritonavir or cobicistat may be sub-optimal. In vitro evidence suggests that ritonavir may also antagonize 17-β estradiol [125] , the currently preferred form of estrogen supplementation for FHT. Similarly, due to increased CVD risk in HIV and with estrogens (see above), abacavir-containing regimens may be suboptimal.…”
Section: Optimization Of Artmentioning
confidence: 99%