Hydroxychloroquine to Prevent Recurrent Congenital Heart Block in Fetuses of Anti-SSA/Ro-Positive Mothers
Experimental and clinical evidence support the role of macrophage Toll-like receptor signaling in maternal anti-SSA/Ro–mediated congenital heart block (CHB). Hydroxychloroquine (HCQ), an orally administered Toll-like receptor antagonist widely used in lupus including during pregnancy, was evaluated...
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creator | Izmirly, Peter Kim, Mimi Friedman, Deborah M. Costedoat-Chalumeau, Nathalie Clancy, Robert Copel, Joshua A. Phoon, Colin K.L. Cuneo, Bettina F. Cohen, Rebecca E. Robins, Kimberly Masson, Mala Wainwright, Benjamin J. Zahr, Noel Saxena, Amit Buyon, Jill P. |
description | Experimental and clinical evidence support the role of macrophage Toll-like receptor signaling in maternal anti-SSA/Ro–mediated congenital heart block (CHB).
Hydroxychloroquine (HCQ), an orally administered Toll-like receptor antagonist widely used in lupus including during pregnancy, was evaluated for efficacy in reducing the historical 18% recurrence rate of CHB.
This multicenter, open-label, single-arm, 2-stage clinical trial was designed using Simon’s optimal approach. Anti-SSA/Ro–positive mothers with a previous pregnancy complicated by CHB were recruited (n = 19 Stage 1; n = 35 Stage 2). Patients received 400 mg daily of HCQ prior to completion of gestational week 10, which was maintained through pregnancy. The primary outcome was 2° or 3° CHB any time during pregnancy, and secondary outcomes included isolated endocardial fibroelastosis, 1° CHB at birth and skin rash.
By intention-to-treat (ITT) analysis, 4 of 54 evaluable pregnancies resulted in a primary outcome (7.4%; 90% confidence interval: 3.4% to 15.9%). Because 9 mothers took potentially confounding medications (fluorinated glucocorticoids and/or intravenous immunoglobulin) after enrollment but prior to a primary outcome, to evaluate HCQ alone, 9 additional mothers were recruited and followed the identical protocol. In the per-protocol analysis restricted to pregnancies exposed to HCQ alone, 4 of 54 (7.4%) fetuses developed a primary outcome as in the ITT. Secondary outcomes included mild endocardial fibroelastosis (n = 1) and cutaneous neonatal lupus (n = 4).
These prospective data support that HCQ significantly reduces the recurrence of CHB below the historical rate by >50%, suggesting that this drug should be prescribed for secondary prevention of fetal cardiac disease in anti-SSA/Ro-exposed pregnancies. (Preventive Approach to Congenital Heart Block With Hydroxychloroquine [PATCH]; NCT01379573)
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doi_str_mv | 10.1016/j.jacc.2020.05.045 |
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Hydroxychloroquine (HCQ), an orally administered Toll-like receptor antagonist widely used in lupus including during pregnancy, was evaluated for efficacy in reducing the historical 18% recurrence rate of CHB.
This multicenter, open-label, single-arm, 2-stage clinical trial was designed using Simon’s optimal approach. Anti-SSA/Ro–positive mothers with a previous pregnancy complicated by CHB were recruited (n = 19 Stage 1; n = 35 Stage 2). Patients received 400 mg daily of HCQ prior to completion of gestational week 10, which was maintained through pregnancy. The primary outcome was 2° or 3° CHB any time during pregnancy, and secondary outcomes included isolated endocardial fibroelastosis, 1° CHB at birth and skin rash.
By intention-to-treat (ITT) analysis, 4 of 54 evaluable pregnancies resulted in a primary outcome (7.4%; 90% confidence interval: 3.4% to 15.9%). Because 9 mothers took potentially confounding medications (fluorinated glucocorticoids and/or intravenous immunoglobulin) after enrollment but prior to a primary outcome, to evaluate HCQ alone, 9 additional mothers were recruited and followed the identical protocol. In the per-protocol analysis restricted to pregnancies exposed to HCQ alone, 4 of 54 (7.4%) fetuses developed a primary outcome as in the ITT. Secondary outcomes included mild endocardial fibroelastosis (n = 1) and cutaneous neonatal lupus (n = 4).
These prospective data support that HCQ significantly reduces the recurrence of CHB below the historical rate by >50%, suggesting that this drug should be prescribed for secondary prevention of fetal cardiac disease in anti-SSA/Ro-exposed pregnancies. (Preventive Approach to Congenital Heart Block With Hydroxychloroquine [PATCH]; NCT01379573)
[Display omitted]</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/j.jacc.2020.05.045</identifier><identifier>PMID: 32674792</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Administration, Oral ; Adult ; anti-SSA/Ro antibodies ; Autoantibodies - immunology ; congenital heart block ; Dose-Response Relationship, Drug ; Enzyme Inhibitors - administration & dosage ; Female ; Fetal Diseases - prevention & control ; Follow-Up Studies ; Heart Block - congenital ; Heart Block - drug therapy ; Heart Block - embryology ; Humans ; hydroxychloroquine ; Hydroxychloroquine - administration & dosage ; Infant, Newborn ; Male ; neonatal lupus ; Pregnancy ; prevention ; Prospective Studies ; Secondary Prevention - methods</subject><ispartof>Journal of the American College of Cardiology, 2020-07, Vol.76 (3), p.292-302</ispartof><rights>2020 American College of Cardiology Foundation</rights><rights>Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-12c569229505c9bf613963e334a4cdd06acf21043ed8bb1c1b2b38ef37ef80673</citedby><cites>FETCH-LOGICAL-c455t-12c569229505c9bf613963e334a4cdd06acf21043ed8bb1c1b2b38ef37ef80673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jacc.2020.05.045$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32674792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Izmirly, Peter</creatorcontrib><creatorcontrib>Kim, Mimi</creatorcontrib><creatorcontrib>Friedman, Deborah M.</creatorcontrib><creatorcontrib>Costedoat-Chalumeau, Nathalie</creatorcontrib><creatorcontrib>Clancy, Robert</creatorcontrib><creatorcontrib>Copel, Joshua A.</creatorcontrib><creatorcontrib>Phoon, Colin K.L.</creatorcontrib><creatorcontrib>Cuneo, Bettina F.</creatorcontrib><creatorcontrib>Cohen, Rebecca E.</creatorcontrib><creatorcontrib>Robins, Kimberly</creatorcontrib><creatorcontrib>Masson, Mala</creatorcontrib><creatorcontrib>Wainwright, Benjamin J.</creatorcontrib><creatorcontrib>Zahr, Noel</creatorcontrib><creatorcontrib>Saxena, Amit</creatorcontrib><creatorcontrib>Buyon, Jill P.</creatorcontrib><title>Hydroxychloroquine to Prevent Recurrent Congenital Heart Block in Fetuses of Anti-SSA/Ro-Positive Mothers</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>Experimental and clinical evidence support the role of macrophage Toll-like receptor signaling in maternal anti-SSA/Ro–mediated congenital heart block (CHB).
Hydroxychloroquine (HCQ), an orally administered Toll-like receptor antagonist widely used in lupus including during pregnancy, was evaluated for efficacy in reducing the historical 18% recurrence rate of CHB.
This multicenter, open-label, single-arm, 2-stage clinical trial was designed using Simon’s optimal approach. Anti-SSA/Ro–positive mothers with a previous pregnancy complicated by CHB were recruited (n = 19 Stage 1; n = 35 Stage 2). Patients received 400 mg daily of HCQ prior to completion of gestational week 10, which was maintained through pregnancy. The primary outcome was 2° or 3° CHB any time during pregnancy, and secondary outcomes included isolated endocardial fibroelastosis, 1° CHB at birth and skin rash.
By intention-to-treat (ITT) analysis, 4 of 54 evaluable pregnancies resulted in a primary outcome (7.4%; 90% confidence interval: 3.4% to 15.9%). Because 9 mothers took potentially confounding medications (fluorinated glucocorticoids and/or intravenous immunoglobulin) after enrollment but prior to a primary outcome, to evaluate HCQ alone, 9 additional mothers were recruited and followed the identical protocol. In the per-protocol analysis restricted to pregnancies exposed to HCQ alone, 4 of 54 (7.4%) fetuses developed a primary outcome as in the ITT. Secondary outcomes included mild endocardial fibroelastosis (n = 1) and cutaneous neonatal lupus (n = 4).
These prospective data support that HCQ significantly reduces the recurrence of CHB below the historical rate by >50%, suggesting that this drug should be prescribed for secondary prevention of fetal cardiac disease in anti-SSA/Ro-exposed pregnancies. (Preventive Approach to Congenital Heart Block With Hydroxychloroquine [PATCH]; NCT01379573)
[Display omitted]</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>anti-SSA/Ro antibodies</subject><subject>Autoantibodies - immunology</subject><subject>congenital heart block</subject><subject>Dose-Response Relationship, Drug</subject><subject>Enzyme Inhibitors - administration & dosage</subject><subject>Female</subject><subject>Fetal Diseases - prevention & control</subject><subject>Follow-Up Studies</subject><subject>Heart Block - congenital</subject><subject>Heart Block - drug therapy</subject><subject>Heart Block - embryology</subject><subject>Humans</subject><subject>hydroxychloroquine</subject><subject>Hydroxychloroquine - administration & dosage</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>neonatal lupus</subject><subject>Pregnancy</subject><subject>prevention</subject><subject>Prospective Studies</subject><subject>Secondary Prevention - methods</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kGFP2zAQhq1p0yiMP8AH5D-QcLbjJJamSV01KBITVRmfLce5UHchZrZbrf-eVAW0feHTnXTv-97dQ8gZg5wBKy_W-dpYm3PgkIPMoZAfyIRJWWdCquojmUAlZMZAVUfkOMY1AJQ1U5_JkeBlVVSKT4ib79rg_-7sqvfB_9m4AWnydBFwi0OiS7SbEPbdzA8POLhkejpHExL93nv7m7qBXmLaRIzUd3Q6JJfd3U0vlj5b-OiS2yL96dMKQ_xCPnWmj3j6Uk_I_eWPX7N5dnN7dT2b3mS2kDJljFtZKs6VBGlV05VMqFKgEIUpbNtCaWzHGRQC27ppmGUNb0SNnaiwq6GsxAn5dsh92jSP2Nrx-GB6_RTcowk77Y3T_08Gt9IPfqsroYqR5RjADwE2-BgDdm9eBnoPXq_1Hrzeg9cg9Qh-NJ3_u_XN8kp6FHw9CHD8fesw6GgdDhZbF9Am3Xr3Xv4z5WCW0g</recordid><startdate>20200721</startdate><enddate>20200721</enddate><creator>Izmirly, Peter</creator><creator>Kim, Mimi</creator><creator>Friedman, Deborah M.</creator><creator>Costedoat-Chalumeau, Nathalie</creator><creator>Clancy, Robert</creator><creator>Copel, Joshua A.</creator><creator>Phoon, Colin K.L.</creator><creator>Cuneo, Bettina F.</creator><creator>Cohen, Rebecca E.</creator><creator>Robins, Kimberly</creator><creator>Masson, Mala</creator><creator>Wainwright, Benjamin J.</creator><creator>Zahr, Noel</creator><creator>Saxena, Amit</creator><creator>Buyon, Jill P.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20200721</creationdate><title>Hydroxychloroquine to Prevent Recurrent Congenital Heart Block in Fetuses of Anti-SSA/Ro-Positive Mothers</title><author>Izmirly, Peter ; 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Hydroxychloroquine (HCQ), an orally administered Toll-like receptor antagonist widely used in lupus including during pregnancy, was evaluated for efficacy in reducing the historical 18% recurrence rate of CHB.
This multicenter, open-label, single-arm, 2-stage clinical trial was designed using Simon’s optimal approach. Anti-SSA/Ro–positive mothers with a previous pregnancy complicated by CHB were recruited (n = 19 Stage 1; n = 35 Stage 2). Patients received 400 mg daily of HCQ prior to completion of gestational week 10, which was maintained through pregnancy. The primary outcome was 2° or 3° CHB any time during pregnancy, and secondary outcomes included isolated endocardial fibroelastosis, 1° CHB at birth and skin rash.
By intention-to-treat (ITT) analysis, 4 of 54 evaluable pregnancies resulted in a primary outcome (7.4%; 90% confidence interval: 3.4% to 15.9%). Because 9 mothers took potentially confounding medications (fluorinated glucocorticoids and/or intravenous immunoglobulin) after enrollment but prior to a primary outcome, to evaluate HCQ alone, 9 additional mothers were recruited and followed the identical protocol. In the per-protocol analysis restricted to pregnancies exposed to HCQ alone, 4 of 54 (7.4%) fetuses developed a primary outcome as in the ITT. Secondary outcomes included mild endocardial fibroelastosis (n = 1) and cutaneous neonatal lupus (n = 4).
These prospective data support that HCQ significantly reduces the recurrence of CHB below the historical rate by >50%, suggesting that this drug should be prescribed for secondary prevention of fetal cardiac disease in anti-SSA/Ro-exposed pregnancies. (Preventive Approach to Congenital Heart Block With Hydroxychloroquine [PATCH]; NCT01379573)
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subjects | Administration, Oral Adult anti-SSA/Ro antibodies Autoantibodies - immunology congenital heart block Dose-Response Relationship, Drug Enzyme Inhibitors - administration & dosage Female Fetal Diseases - prevention & control Follow-Up Studies Heart Block - congenital Heart Block - drug therapy Heart Block - embryology Humans hydroxychloroquine Hydroxychloroquine - administration & dosage Infant, Newborn Male neonatal lupus Pregnancy prevention Prospective Studies Secondary Prevention - methods |
title | Hydroxychloroquine to Prevent Recurrent Congenital Heart Block in Fetuses of Anti-SSA/Ro-Positive Mothers |
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