Extra-criteria clinical manifestations of antiphospholipid antibody should not be ignored
The clinical symptoms of APS include many non-thrombotic manifestations, also called extra-criteria manifestations, including thrombocytopenia, aPL nephropathy, livedo reticularis, valve heart disease, and neurological manifestations. While thrombosis occurred in 44 (24.4%) patients and pregnant mor...
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Published in | Chinese medical journal Vol. 135; no. 18; pp. 2251 - 2252 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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China
Lippincott Williams & Wilkins
20.09.2022
Lippincott Williams & Wilkins Ovid Technologies Wolters Kluwer |
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Abstract | The clinical symptoms of APS include many non-thrombotic manifestations, also called extra-criteria manifestations, including thrombocytopenia, aPL nephropathy, livedo reticularis, valve heart disease, and neurological manifestations. While thrombosis occurred in 44 (24.4%) patients and pregnant morbidity in 17 (9.4%), 119 (66.1%) patients were just persistent aPL positive only, 77 (42.8%) were totally asymptomatic, and 42 (23.3%) presented extra-criteria manifestations independently. Since there were also 30 APS patients with extra-criteria manifestations, the total frequencies of aPL associated extra-criteria manifestations were 40% (72/180). The most common extra-criteria manifestations were thrombocytopenia (31.7%), neurological manifestations (10.0%), and valve heart disease (8.3%), they were more common in secondary APS compared with primary APS and non-APS-aPL+ patients [Table 1]. Items All (n = 180) PAPS (n = 27) SAPS (n = 34) Non-APS aPL+ (n = 119) P values Female, n (%) 131 (72.8) 18 (66.7) 26 (76.5) 87 (73.1) 0.687 Age (years), mean (SD) 40.3 (17.6) 37.8 (11.0) 37.7 (15.4) 41.6 (19.4) 0.384 Anti-β2GPI antibody, n (%) 149 (82.8) 25 (92.6) 29 (85.3) 95 (79.8) 0.259 aCL, n (%) 107 (59.4) 18 (66.7) 24 (70.6) 65 (54.6) 0.175 LA, n (%) 65 (36.1) 13 (48.1) 17 (50) 35 (29.4) 0.032 Triple aPL+, n (%) 46 (25.6) 11 (40.7) 14 (41.2) 21 (17.6) 0.003 pt w/extra-criteria, n (%) 72 (40.0) 9 (33.3) 21 (61.8) 42 (35.3) 0.016 Thrombocytopenia, n (%) 57 (31.7) 6 (22.2) 18 (52.9) 33 (27.7) 0.011 Livedo reticularis, n (%) 3 (1.7) 0 (0) 2 (6.5) 1 (0.8) 0.151 APL nephrology, n (%) 6 (3.3) 2 (7.4) 4 (12.9) 0 (0) 0.001 Valve heart disease, n (%) 15 (8.3) 2 (7.4) 7 (20.6) 6 (5.0) 0.015 Neurological, n (%) 18 (10) 3 (11.1) 8 (23.5) 7 (5.9) 0.010 Fisher's exact test. aCL: [...]40% aPL-positive patients presented with extra-criteria manifestations regardless of thrombotic or obstetric events, more common in SLE patients. |
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AbstractList | The clinical symptoms of APS include many non-thrombotic manifestations, also called extra-criteria manifestations, including thrombocytopenia, aPL nephropathy, livedo reticularis, valve heart disease, and neurological manifestations. While thrombosis occurred in 44 (24.4%) patients and pregnant morbidity in 17 (9.4%), 119 (66.1%) patients were just persistent aPL positive only, 77 (42.8%) were totally asymptomatic, and 42 (23.3%) presented extra-criteria manifestations independently. Since there were also 30 APS patients with extra-criteria manifestations, the total frequencies of aPL associated extra-criteria manifestations were 40% (72/180). The most common extra-criteria manifestations were thrombocytopenia (31.7%), neurological manifestations (10.0%), and valve heart disease (8.3%), they were more common in secondary APS compared with primary APS and non-APS-aPL+ patients [Table 1]. Items All (n = 180) PAPS (n = 27) SAPS (n = 34) Non-APS aPL+ (n = 119) P values Female, n (%) 131 (72.8) 18 (66.7) 26 (76.5) 87 (73.1) 0.687 Age (years), mean (SD) 40.3 (17.6) 37.8 (11.0) 37.7 (15.4) 41.6 (19.4) 0.384 Anti-β2GPI antibody, n (%) 149 (82.8) 25 (92.6) 29 (85.3) 95 (79.8) 0.259 aCL, n (%) 107 (59.4) 18 (66.7) 24 (70.6) 65 (54.6) 0.175 LA, n (%) 65 (36.1) 13 (48.1) 17 (50) 35 (29.4) 0.032 Triple aPL+, n (%) 46 (25.6) 11 (40.7) 14 (41.2) 21 (17.6) 0.003 pt w/extra-criteria, n (%) 72 (40.0) 9 (33.3) 21 (61.8) 42 (35.3) 0.016 Thrombocytopenia, n (%) 57 (31.7) 6 (22.2) 18 (52.9) 33 (27.7) 0.011 Livedo reticularis, n (%) 3 (1.7) 0 (0) 2 (6.5) 1 (0.8) 0.151 APL nephrology, n (%) 6 (3.3) 2 (7.4) 4 (12.9) 0 (0) 0.001 Valve heart disease, n (%) 15 (8.3) 2 (7.4) 7 (20.6) 6 (5.0) 0.015 Neurological, n (%) 18 (10) 3 (11.1) 8 (23.5) 7 (5.9) 0.010 Fisher's exact test. aCL: [...]40% aPL-positive patients presented with extra-criteria manifestations regardless of thrombotic or obstetric events, more common in SLE patients. |
Author | Huang, Can Tian, Xinping Li, Mengtao Zeng, Xiaofeng Wang, Qian Zhao, Jiuliang Hu, Chaojun |
AuthorAffiliation | 1 Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China 3 State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Beijing 100730, China 4 Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing 100730, China 2 National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science and Technology, Beijing 100730, China |
AuthorAffiliation_xml | – name: 1 Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – name: 3 State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Beijing 100730, China – name: 4 Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing 100730, China – name: 2 National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science and Technology, Beijing 100730, China |
Author_xml | – sequence: 1 givenname: Can surname: Huang fullname: Huang, Can organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – sequence: 2 givenname: Chaojun surname: Hu fullname: Hu, Chaojun organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – sequence: 3 givenname: Jiuliang surname: Zhao fullname: Zhao, Jiuliang organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – sequence: 4 givenname: Qian surname: Wang fullname: Wang, Qian organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – sequence: 5 givenname: Xinping surname: Tian fullname: Tian, Xinping organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – sequence: 6 givenname: Mengtao surname: Li fullname: Li, Mengtao organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China – sequence: 7 givenname: Xiaofeng surname: Zeng fullname: Zeng, Xiaofeng organization: Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China |
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Cites_doi | 10.1007/s12026-019-09110-x 10.1016/j.autrev.2015.01.002 10.1016/j.semarthrit.2017.12.006 10.1038/nrrheum.2017.124 |
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References_xml | – volume: 67 start-page: 478 year: 2019 ident: R2-20250603 article-title: A high-risk laboratory profile of antiphospholipid antibodies and thrombosis is associated with a large number of extra-criteria manifestations in obstetric antiphospholipid syndrome publication-title: Immunol Res doi: 10.1007/s12026-019-09110-x – volume: 14 start-page: 401 year: 2015 ident: R4-20250603 article-title: The relevance of “non-criteria” clinical manifestations of antiphospholipid syndrome: 14th International Congress on Antiphospholipid Antibodies Technical Task Force Report on Antiphospholipid Syndrome Clinical Features publication-title: Autoimmun Rev doi: 10.1016/j.autrev.2015.01.002 – volume: 31 start-page: 234 year: 2013 ident: R3-20250603 article-title: Association between systemic non-criteria APS manifestations and antibody type and level: results from the Serbian national cohort study publication-title: Clin Exp Rheumatol – volume: 48 start-page: 117 year: 2018 ident: R5-20250603 article-title: Extra-criteria manifestations of antiphospholipid syndrome: risk assessment and management publication-title: Semin Arthritis Rheum doi: 10.1016/j.semarthrit.2017.12.006 – volume: 13 start-page: 548 year: 2017 ident: R1-20250603 article-title: Diagnosing antiphospholipid syndrome: “Extra-criteria” manifestations and technical advances publication-title: Nat Rev Rheumatol doi: 10.1038/nrrheum.2017.124 |
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SubjectTerms | Antibodies Antibodies, Antiphospholipid Anticoagulants Antiphospholipid Syndrome - diagnosis Antiphospholipid Syndrome - drug therapy Cardiovascular disease Correspondence Glycoproteins Heart Humans Lupus Migraine Obstetrics Thrombocytopenia Thrombosis |
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Title | Extra-criteria clinical manifestations of antiphospholipid antibody should not be ignored |
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