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This study was undertaken to develop a clearer understanding of the association between changes in disease activity and lipid levels in <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content>, which may inform <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content> risk stratification in this population.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Lipid levels were assessed in stored serum samples (obtained at baseline and month 6) from the Rituximab for <jats:styled-content style=\"fixed-case\">ANCA<\/jats:styled-content>\u2010Associated Vasculitis (<jats:styled-content style=\"fixed-case\">RAVE<\/jats:styled-content>) trial, which randomized patients to receive either rituximab or cyclophosphamide followed by azathioprine. Paired <jats:italic>t<\/jats:italic>\u2010tests and multivariable linear regression were used to assess changes in lipid levels.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Of the 142 patients with serum samples available, the mean \u00b1 <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content> age was 52.3 \u00b1 14.7 years, 72 (51%) were male, 95 (67%) were proteinase 3 (<jats:styled-content style=\"fixed-case\">PR<\/jats:styled-content>3)\u2013<jats:styled-content style=\"fixed-case\">ANCA<\/jats:styled-content> positive, 72 (51%) had received a new diagnosis of <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content>, and 75 (53%) were treated with rituximab. Several lipid levels increased between baseline and month 6, including total cholesterol (+12.4 mg\/dl [95% confidence interval (95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>) +7.1, +21.0]), low\u2010density lipoprotein (+10.3 mg\/dl [95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> +6.1, +17.1]), and apolipoprotein B (+3.5 mg\/dl [95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> +1.0, +8.3]). These changes were observed among newly diagnosed and <jats:styled-content style=\"fixed-case\">PR<\/jats:styled-content>3\u2010<jats:styled-content style=\"fixed-case\">ANCA<\/jats:styled-content>\u2013positive patients but not among those with relapsing disease or myeloperoxidase\u2010<jats:styled-content style=\"fixed-case\">ANCA<\/jats:styled-content>\u2013positive patients. There was no difference in change in lipid levels between rituximab\u2010treated patients and cyclophosphamide\u2010treated patients. Changes in lipid levels correlated with changes in erythrocyte sedimentation rate but not with other inflammatory markers or glucocorticoid exposure.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Lipid levels increased during remission induction among patients with newly diagnosed <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content> and those who were <jats:styled-content style=\"fixed-case\">PR<\/jats:styled-content>3\u2010<jats:styled-content style=\"fixed-case\">ANCA<\/jats:styled-content> positive. Disease activity and <jats:styled-content style=\"fixed-case\">ANCA<\/jats:styled-content> type should be considered when assessing lipid profiles to stratify <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content> risk in patients with <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1002\/art.41006","type":"journal-article","created":{"date-parts":[[2019,6,4]],"date-time":"2019-06-04T08:00:49Z","timestamp":1559635249000},"page":"1879-1887","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":33,"title":["Disease Activity, Antineutrophil Cytoplasmic Antibody Type, and Lipid Levels in Antineutrophil Cytoplasmic Antibody\u2013Associated Vasculitis"],"prefix":"10.1002","volume":"71","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4708-7038","authenticated-orcid":false,"given":"Zachary S.","family":"Wallace","sequence":"first","affiliation":[{"name":"Massachusetts General Hospital  Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaoqing","family":"Fu","sequence":"additional","affiliation":[{"name":"Massachusetts General Hospital  Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4797-3200","authenticated-orcid":false,"given":"Katherine","family":"Liao","sequence":"additional","affiliation":[{"name":"Brigham and Women's Hospital  Boston Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cees G. 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