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DOI 10.1016/j.jacl.2016.10.013

Медицинская библиотека · Journal of clinical lipidology · 2016

Lipoprotein-X in cholestatic patients causes xanthomas and promotes foam cell formation in human macrophages.

Suzuki Luka, Hirayama Satoshi, Fukui Mariko, Sasaki Makoto, Hiroi Sadayuki, Ayaori Makoto, Terai Shuji, Tozuka Minoru, Watada Hirotaka, Miida Takashi

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Lipoprotein-X (Lp-X) is an abnormal phospholipid-rich lipoprotein found in patients with cholestatic liver disease. Some patients exhibit skin xanthomas and severe hyperlipidemia.

OBJECTIVE

We investigated whether Lp-X induces foam cell formation in human-derived macrophages.

METHODS

To compare the atherogenic properties of Lp-X and modified LDL, we isolated Lp-X from 2 patients who had drug-induced cholestasis and xanthoma striata in the interphalangeal folds. We prepared oxidized LDL and acetylated LDL from healthy volunteers for the positive control experiments.

RESULTS

When human monocyte-derived macrophages were incubated with these lipoproteins, the isolated Lp-X induced more prominent lipid accumulation than oxidized LDL or acetylated LDL. One case underwent liver biopsy, with the bile ducts showing marked damage, fulfilling the criteria for vanishing bile duct syndrome. The other case was clinically diagnosed as drug-induced hypersensitivity syndrome. In both cases, Lp-X levels decreased markedly and the xanthomas disappeared completely after the improvement of cholestasis.

CONCLUSION

This study indicates that Lp-X induces foam cell formation in human-derived macrophages. Our findings strongly suggest that persistently elevated Lp-X may cause xanthomas.

Для цитирования: Suzuki Luka, Hirayama Satoshi, Fukui Mariko, Sasaki Makoto, Hiroi Sadayuki, Ayaori Makoto, Terai Shuji, Tozuka Minoru, Watada Hirotaka, Miida Takashi. Lipoprotein-X in cholestatic patients causes xanthomas and promotes foam cell formation in human macrophages.. Journal of clinical lipidology. 2016. DOI: 10.1016/j.jacl.2016.10.013.

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