Hydroxychloroquine increased cholesterol transfer to high-density lipoprotein in systemic lupus erythematosus: A possible mechanism for the reversal of atherosclerosis in the disease

Introduction The beneficial effect of hydroxychloroquine (HCQ) in decreasing LDL levels on Systemic Lupus Erythematosus (SLE) is well defined. The influence of this drug on HDL levels is still under debate and information about its effect on cholesterol reverse transport is lacking. Objective To eva...

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Veröffentlicht in:Lupus 2022-05, Vol.31 (6), p.659-665
Hauptverfasser: Lang, Maria G, Vinagre, Carmen GC, Bonfa, Eloisa, Freitas, Fatima R, Pasoto, Sandra G, Brito, Tatiane S, Seguro, Luciana PC, Maranhão, Raul C, Borba, Eduardo F
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container_end_page 665
container_issue 6
container_start_page 659
container_title Lupus
container_volume 31
creator Lang, Maria G
Vinagre, Carmen GC
Bonfa, Eloisa
Freitas, Fatima R
Pasoto, Sandra G
Brito, Tatiane S
Seguro, Luciana PC
Maranhão, Raul C
Borba, Eduardo F
description Introduction The beneficial effect of hydroxychloroquine (HCQ) in decreasing LDL levels on Systemic Lupus Erythematosus (SLE) is well defined. The influence of this drug on HDL levels is still under debate and information about its effect on cholesterol reverse transport is lacking. Objective To evaluate the effects of HCQ on HDL levels and the transfer of lipids to this lipoprotein in SLE. Methods Nineteen SLE patients using only HCQ (SLE WITH HCQ), 19 SLE patients without any therapy (SLE WITHOUT THERAPY), and 19 healthy controls (CONTROL) were included. All three groups were premenopausal women age- and gender-matched. Serum lipids and apolipoproteins were determined by commercial kits. An in vitro transfer of four lipids (14C-Phospolipid, 3H-Cholesteryl ester, 3H-Triglyceride, and 14C-Unesterified cholesterol) from a radioactively labeled nanoemulsion donor to HDL was performed in all participants. Results Groups had comparable mean age, weight, height, BMI(body mass index), and waist circumference (p > .05). Mean HDL levels were higher in SLE WITH HCQ group compared to SLE WITHOUT THERAPY(58.37 ± 14.04 vs 49.79 ± 8.0 mg/dL; p < .05) but lower than CONTROL (58.37 ± 14.04 vs 68.58 ± 9.99 mg/dL; p < .05). Total cholesterol (TC) and LDL levels were also significantly lower in SLE WITH HCQ compared SLE WITHOUT THERAPY(148.16 ± 16.43 vs 167.11 ± 30.18 mg/dL; p < .05, 75.05 ± 22.52 vs 96.05 ± 25.63 mg/dL; p < .05) and CONTROL (148.16 ± 16.43 vs 174.11 ± 23.70 mg/dL; p < .05, 75.05 ± 22.52 vs 88.53 ± 20.24 mg/dL; p < .05). The in vitro lipid transfer to HDL study revealed a significant difference among the three groups (p = .002) with a higher transfer of unesterified cholesterol(UC) in SLE WITH HCQ compared to SLE WITHOUT THERAPY(5.40 ± 1.05% vs. 4.44 ± 1.05%; p < .05). The latter was significantly decreased compared to CONTROL (5.40 ± 1.05% vs. 5.99 ± 1.71%; p < .05).The percentages of transfer of triacylglycerol (4.93 ± 0.69% vs. 4.50 ± 0.69% vs. 5.14 ± 1.01%; p = .054), esterified cholesterol (5.24 ± 0.70% vs. 4.96 ± 0.89% vs. 5.69 ± 1.27%; p = .079), and phospholipid (15.67 ± 1.03% vs. 15.34 ± 1.44% vs. 16.47 ± 1.89%; p = .066) were similar among groups. Conclusion The present study is the first to demonstrate that HCQ promoted a higher transfer of unesterified cholesterol which may account for the increased HDL levels in lupus patients under HCQ. This desirable effect may underlie the reported reduced atherosclerosis in SLE.
doi_str_mv 10.1177/09612033221090127
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The influence of this drug on HDL levels is still under debate and information about its effect on cholesterol reverse transport is lacking. Objective To evaluate the effects of HCQ on HDL levels and the transfer of lipids to this lipoprotein in SLE. Methods Nineteen SLE patients using only HCQ (SLE WITH HCQ), 19 SLE patients without any therapy (SLE WITHOUT THERAPY), and 19 healthy controls (CONTROL) were included. All three groups were premenopausal women age- and gender-matched. Serum lipids and apolipoproteins were determined by commercial kits. An in vitro transfer of four lipids (14C-Phospolipid, 3H-Cholesteryl ester, 3H-Triglyceride, and 14C-Unesterified cholesterol) from a radioactively labeled nanoemulsion donor to HDL was performed in all participants. Results Groups had comparable mean age, weight, height, BMI(body mass index), and waist circumference (p > .05). Mean HDL levels were higher in SLE WITH HCQ group compared to SLE WITHOUT THERAPY(58.37 ± 14.04 vs 49.79 ± 8.0 mg/dL; p < .05) but lower than CONTROL (58.37 ± 14.04 vs 68.58 ± 9.99 mg/dL; p < .05). Total cholesterol (TC) and LDL levels were also significantly lower in SLE WITH HCQ compared SLE WITHOUT THERAPY(148.16 ± 16.43 vs 167.11 ± 30.18 mg/dL; p < .05, 75.05 ± 22.52 vs 96.05 ± 25.63 mg/dL; p < .05) and CONTROL (148.16 ± 16.43 vs 174.11 ± 23.70 mg/dL; p < .05, 75.05 ± 22.52 vs 88.53 ± 20.24 mg/dL; p < .05). The in vitro lipid transfer to HDL study revealed a significant difference among the three groups (p = .002) with a higher transfer of unesterified cholesterol(UC) in SLE WITH HCQ compared to SLE WITHOUT THERAPY(5.40 ± 1.05% vs. 4.44 ± 1.05%; p < .05). The latter was significantly decreased compared to CONTROL (5.40 ± 1.05% vs. 5.99 ± 1.71%; p < .05).The percentages of transfer of triacylglycerol (4.93 ± 0.69% vs. 4.50 ± 0.69% vs. 5.14 ± 1.01%; p = .054), esterified cholesterol (5.24 ± 0.70% vs. 4.96 ± 0.89% vs. 5.69 ± 1.27%; p = .079), and phospholipid (15.67 ± 1.03% vs. 15.34 ± 1.44% vs. 16.47 ± 1.89%; p = .066) were similar among groups. Conclusion The present study is the first to demonstrate that HCQ promoted a higher transfer of unesterified cholesterol which may account for the increased HDL levels in lupus patients under HCQ. This desirable effect may underlie the reported reduced atherosclerosis in SLE.]]></description><identifier>ISSN: 0961-2033</identifier><identifier>EISSN: 1477-0962</identifier><identifier>DOI: 10.1177/09612033221090127</identifier><identifier>PMID: 35332823</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Apolipoproteins ; Arteriosclerosis ; Atherosclerosis ; Body mass index ; Cholesterol ; Emulsions ; High density lipoprotein ; Hydroxychloroquine ; Lipids ; Low density lipoprotein ; Lupus ; Phospholipids ; Serum lipids ; Systemic lupus erythematosus</subject><ispartof>Lupus, 2022-05, Vol.31 (6), p.659-665</ispartof><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-b4333fbb4d218aba43c5c3d1f6e6e078fe791c6c020cedd21821c7f180a7daad3</citedby><cites>FETCH-LOGICAL-c368t-b4333fbb4d218aba43c5c3d1f6e6e078fe791c6c020cedd21821c7f180a7daad3</cites><orcidid>0000-0002-0520-4681 ; 0000-0002-1285-0796 ; 0000-0001-6194-5129 ; 0000-0002-7343-6804</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/09612033221090127$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/09612033221090127$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35332823$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lang, Maria G</creatorcontrib><creatorcontrib>Vinagre, Carmen GC</creatorcontrib><creatorcontrib>Bonfa, Eloisa</creatorcontrib><creatorcontrib>Freitas, Fatima R</creatorcontrib><creatorcontrib>Pasoto, Sandra G</creatorcontrib><creatorcontrib>Brito, Tatiane S</creatorcontrib><creatorcontrib>Seguro, Luciana PC</creatorcontrib><creatorcontrib>Maranhão, Raul C</creatorcontrib><creatorcontrib>Borba, Eduardo F</creatorcontrib><title>Hydroxychloroquine increased cholesterol transfer to high-density lipoprotein in systemic lupus erythematosus: A possible mechanism for the reversal of atherosclerosis in the disease</title><title>Lupus</title><addtitle>Lupus</addtitle><description><![CDATA[Introduction The beneficial effect of hydroxychloroquine (HCQ) in decreasing LDL levels on Systemic Lupus Erythematosus (SLE) is well defined. The influence of this drug on HDL levels is still under debate and information about its effect on cholesterol reverse transport is lacking. Objective To evaluate the effects of HCQ on HDL levels and the transfer of lipids to this lipoprotein in SLE. Methods Nineteen SLE patients using only HCQ (SLE WITH HCQ), 19 SLE patients without any therapy (SLE WITHOUT THERAPY), and 19 healthy controls (CONTROL) were included. All three groups were premenopausal women age- and gender-matched. Serum lipids and apolipoproteins were determined by commercial kits. An in vitro transfer of four lipids (14C-Phospolipid, 3H-Cholesteryl ester, 3H-Triglyceride, and 14C-Unesterified cholesterol) from a radioactively labeled nanoemulsion donor to HDL was performed in all participants. Results Groups had comparable mean age, weight, height, BMI(body mass index), and waist circumference (p > .05). Mean HDL levels were higher in SLE WITH HCQ group compared to SLE WITHOUT THERAPY(58.37 ± 14.04 vs 49.79 ± 8.0 mg/dL; p < .05) but lower than CONTROL (58.37 ± 14.04 vs 68.58 ± 9.99 mg/dL; p < .05). Total cholesterol (TC) and LDL levels were also significantly lower in SLE WITH HCQ compared SLE WITHOUT THERAPY(148.16 ± 16.43 vs 167.11 ± 30.18 mg/dL; p < .05, 75.05 ± 22.52 vs 96.05 ± 25.63 mg/dL; p < .05) and CONTROL (148.16 ± 16.43 vs 174.11 ± 23.70 mg/dL; p < .05, 75.05 ± 22.52 vs 88.53 ± 20.24 mg/dL; p < .05). The in vitro lipid transfer to HDL study revealed a significant difference among the three groups (p = .002) with a higher transfer of unesterified cholesterol(UC) in SLE WITH HCQ compared to SLE WITHOUT THERAPY(5.40 ± 1.05% vs. 4.44 ± 1.05%; p < .05). The latter was significantly decreased compared to CONTROL (5.40 ± 1.05% vs. 5.99 ± 1.71%; p < .05).The percentages of transfer of triacylglycerol (4.93 ± 0.69% vs. 4.50 ± 0.69% vs. 5.14 ± 1.01%; p = .054), esterified cholesterol (5.24 ± 0.70% vs. 4.96 ± 0.89% vs. 5.69 ± 1.27%; p = .079), and phospholipid (15.67 ± 1.03% vs. 15.34 ± 1.44% vs. 16.47 ± 1.89%; p = .066) were similar among groups. Conclusion The present study is the first to demonstrate that HCQ promoted a higher transfer of unesterified cholesterol which may account for the increased HDL levels in lupus patients under HCQ. This desirable effect may underlie the reported reduced atherosclerosis in SLE.]]></description><subject>Apolipoproteins</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Body mass index</subject><subject>Cholesterol</subject><subject>Emulsions</subject><subject>High density lipoprotein</subject><subject>Hydroxychloroquine</subject><subject>Lipids</subject><subject>Low density lipoprotein</subject><subject>Lupus</subject><subject>Phospholipids</subject><subject>Serum lipids</subject><subject>Systemic lupus erythematosus</subject><issn>0961-2033</issn><issn>1477-0962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1TAQhS1ERS-FB2CDLLFhk9Y_uXEuu6oCilSJTbuOHHvcuHLi4ElQ82I8H7ZuAQnExpY83zkznkPIG87OOVfqgh0aLpiUQnB2YFyoZ2THa6WqXBDPya7UqwKckpeID4wxyQ_NC3Iq91nUCrkjP643m-LjZoYQU_y2-gmon0wCjWCpGWIAXCDFQJekJ3SQ6BLp4O-HysKEftlo8HOcU1zAT1lKccuC0Rsa1nlFCmlbBhj1EnHFD_SSzhHR9wHoCGbQk8eRuphdB6AJvkNCHWh0VOeHFNGEcnoszgWxHstor8iJ0wHh9dN9Ru4-fby9uq5uvn7-cnV5UxnZtEvV11JK1_e1FbzVva6l2RtpuWugAaZaB-rATWOYYAZsgQQ3yvGWaWW1tvKMvD_6zmU5eRXd6NFACHqCuGInmrpmQiouMvruL_QhrmnK02VqL_c8J9Nkih8pk7-FCVw3Jz_qtHWcdSXU7p9Qs-btk_Paj2B_K36lmIHzI4D6Hv60_b_jT0ATr1U</recordid><startdate>202205</startdate><enddate>202205</enddate><creator>Lang, Maria G</creator><creator>Vinagre, Carmen GC</creator><creator>Bonfa, Eloisa</creator><creator>Freitas, Fatima R</creator><creator>Pasoto, Sandra G</creator><creator>Brito, Tatiane S</creator><creator>Seguro, Luciana PC</creator><creator>Maranhão, Raul C</creator><creator>Borba, Eduardo F</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0520-4681</orcidid><orcidid>https://orcid.org/0000-0002-1285-0796</orcidid><orcidid>https://orcid.org/0000-0001-6194-5129</orcidid><orcidid>https://orcid.org/0000-0002-7343-6804</orcidid></search><sort><creationdate>202205</creationdate><title>Hydroxychloroquine increased cholesterol transfer to high-density lipoprotein in systemic lupus erythematosus: A possible mechanism for the reversal of atherosclerosis in the disease</title><author>Lang, Maria G ; Vinagre, Carmen GC ; Bonfa, Eloisa ; Freitas, Fatima R ; Pasoto, Sandra G ; Brito, Tatiane S ; Seguro, Luciana PC ; Maranhão, Raul C ; Borba, Eduardo F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-b4333fbb4d218aba43c5c3d1f6e6e078fe791c6c020cedd21821c7f180a7daad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Apolipoproteins</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Body mass index</topic><topic>Cholesterol</topic><topic>Emulsions</topic><topic>High density lipoprotein</topic><topic>Hydroxychloroquine</topic><topic>Lipids</topic><topic>Low density lipoprotein</topic><topic>Lupus</topic><topic>Phospholipids</topic><topic>Serum lipids</topic><topic>Systemic lupus erythematosus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lang, Maria G</creatorcontrib><creatorcontrib>Vinagre, Carmen GC</creatorcontrib><creatorcontrib>Bonfa, Eloisa</creatorcontrib><creatorcontrib>Freitas, Fatima R</creatorcontrib><creatorcontrib>Pasoto, Sandra G</creatorcontrib><creatorcontrib>Brito, Tatiane S</creatorcontrib><creatorcontrib>Seguro, Luciana PC</creatorcontrib><creatorcontrib>Maranhão, Raul C</creatorcontrib><creatorcontrib>Borba, Eduardo F</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Lupus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lang, Maria G</au><au>Vinagre, Carmen GC</au><au>Bonfa, Eloisa</au><au>Freitas, Fatima R</au><au>Pasoto, Sandra G</au><au>Brito, Tatiane S</au><au>Seguro, Luciana PC</au><au>Maranhão, Raul C</au><au>Borba, Eduardo F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydroxychloroquine increased cholesterol transfer to high-density lipoprotein in systemic lupus erythematosus: A possible mechanism for the reversal of atherosclerosis in the disease</atitle><jtitle>Lupus</jtitle><addtitle>Lupus</addtitle><date>2022-05</date><risdate>2022</risdate><volume>31</volume><issue>6</issue><spage>659</spage><epage>665</epage><pages>659-665</pages><issn>0961-2033</issn><eissn>1477-0962</eissn><abstract><![CDATA[Introduction The beneficial effect of hydroxychloroquine (HCQ) in decreasing LDL levels on Systemic Lupus Erythematosus (SLE) is well defined. The influence of this drug on HDL levels is still under debate and information about its effect on cholesterol reverse transport is lacking. Objective To evaluate the effects of HCQ on HDL levels and the transfer of lipids to this lipoprotein in SLE. Methods Nineteen SLE patients using only HCQ (SLE WITH HCQ), 19 SLE patients without any therapy (SLE WITHOUT THERAPY), and 19 healthy controls (CONTROL) were included. All three groups were premenopausal women age- and gender-matched. Serum lipids and apolipoproteins were determined by commercial kits. An in vitro transfer of four lipids (14C-Phospolipid, 3H-Cholesteryl ester, 3H-Triglyceride, and 14C-Unesterified cholesterol) from a radioactively labeled nanoemulsion donor to HDL was performed in all participants. Results Groups had comparable mean age, weight, height, BMI(body mass index), and waist circumference (p > .05). Mean HDL levels were higher in SLE WITH HCQ group compared to SLE WITHOUT THERAPY(58.37 ± 14.04 vs 49.79 ± 8.0 mg/dL; p < .05) but lower than CONTROL (58.37 ± 14.04 vs 68.58 ± 9.99 mg/dL; p < .05). Total cholesterol (TC) and LDL levels were also significantly lower in SLE WITH HCQ compared SLE WITHOUT THERAPY(148.16 ± 16.43 vs 167.11 ± 30.18 mg/dL; p < .05, 75.05 ± 22.52 vs 96.05 ± 25.63 mg/dL; p < .05) and CONTROL (148.16 ± 16.43 vs 174.11 ± 23.70 mg/dL; p < .05, 75.05 ± 22.52 vs 88.53 ± 20.24 mg/dL; p < .05). The in vitro lipid transfer to HDL study revealed a significant difference among the three groups (p = .002) with a higher transfer of unesterified cholesterol(UC) in SLE WITH HCQ compared to SLE WITHOUT THERAPY(5.40 ± 1.05% vs. 4.44 ± 1.05%; p < .05). The latter was significantly decreased compared to CONTROL (5.40 ± 1.05% vs. 5.99 ± 1.71%; p < .05).The percentages of transfer of triacylglycerol (4.93 ± 0.69% vs. 4.50 ± 0.69% vs. 5.14 ± 1.01%; p = .054), esterified cholesterol (5.24 ± 0.70% vs. 4.96 ± 0.89% vs. 5.69 ± 1.27%; p = .079), and phospholipid (15.67 ± 1.03% vs. 15.34 ± 1.44% vs. 16.47 ± 1.89%; p = .066) were similar among groups. Conclusion The present study is the first to demonstrate that HCQ promoted a higher transfer of unesterified cholesterol which may account for the increased HDL levels in lupus patients under HCQ. This desirable effect may underlie the reported reduced atherosclerosis in SLE.]]></abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>35332823</pmid><doi>10.1177/09612033221090127</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0520-4681</orcidid><orcidid>https://orcid.org/0000-0002-1285-0796</orcidid><orcidid>https://orcid.org/0000-0001-6194-5129</orcidid><orcidid>https://orcid.org/0000-0002-7343-6804</orcidid></addata></record>
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source SAGE Complete
subjects Apolipoproteins
Arteriosclerosis
Atherosclerosis
Body mass index
Cholesterol
Emulsions
High density lipoprotein
Hydroxychloroquine
Lipids
Low density lipoprotein
Lupus
Phospholipids
Serum lipids
Systemic lupus erythematosus
title Hydroxychloroquine increased cholesterol transfer to high-density lipoprotein in systemic lupus erythematosus: A possible mechanism for the reversal of atherosclerosis in the disease
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