Javascript must be enabled to continue!
Triple positive profile in antiphospholipid syndrome: prognosis, relapse and management from a retrospective multicentre study
View through CrossRef
Objective
Antiphospholipid syndrome (APS) is defined by the association of thromboembolic and/or obstetrical clinical manifestations and the presence of antiphospholipid antibodies. The objective of our study was to evaluate the impact of the triple-positive profile in a cohort of 204 APS patients.
Methods
We conducted a retrospective study, including patients with primary or secondary APS, meeting the Sydney criteria with at least one thrombotic and/or obstetrical complication. Clinical characteristics and the risk of relapse (defined by the occurrence of a new thrombotic event and/or a new adverse obstetrical event) between triple-positive and non-triple-positive APS patients were compared.
Results
204 patients were included in our study, 68 were triple-positive and 136 were single or double positive. 122 patients (59.8%) had primary APS. 67 patients (32.8%) had obstetrical APS, with a higher rate among triple-positive patients (45.6% vs 26.5%, p=0.010), and 170 patients (83.3%) had thrombotic APS, without difference between triple-positive and others. Thrombotic events were more often venous (56.4%) than arterial (37.7%). Triple-positive patients had more placental complications than others (17.6% vs 2.9%, p=0.001) and more non-criteria events (48.5% vs 25.7%, p=0.002). Among non-criteria events, there was a higher frequency of Sneddon syndrome in triple-positive patients (7.4% vs 0.7%, p=0.028). The relapse rate was higher in triple-positive patients than in others (63.2% vs 39,7%, p=0002). In multivariate analysis, the triple-positive profile was associated with a higher risk of relapse (HR 1.63; 95% CI 1.04 to 2.55; p=0.031).
Conclusion
The triple-positivity is associated with a higher risk of relapse and obstetrical complications.
Title: Triple positive profile in antiphospholipid syndrome: prognosis, relapse and management from a retrospective multicentre study
Description:
Objective
Antiphospholipid syndrome (APS) is defined by the association of thromboembolic and/or obstetrical clinical manifestations and the presence of antiphospholipid antibodies.
The objective of our study was to evaluate the impact of the triple-positive profile in a cohort of 204 APS patients.
Methods
We conducted a retrospective study, including patients with primary or secondary APS, meeting the Sydney criteria with at least one thrombotic and/or obstetrical complication.
Clinical characteristics and the risk of relapse (defined by the occurrence of a new thrombotic event and/or a new adverse obstetrical event) between triple-positive and non-triple-positive APS patients were compared.
Results
204 patients were included in our study, 68 were triple-positive and 136 were single or double positive.
122 patients (59.
8%) had primary APS.
67 patients (32.
8%) had obstetrical APS, with a higher rate among triple-positive patients (45.
6% vs 26.
5%, p=0.
010), and 170 patients (83.
3%) had thrombotic APS, without difference between triple-positive and others.
Thrombotic events were more often venous (56.
4%) than arterial (37.
7%).
Triple-positive patients had more placental complications than others (17.
6% vs 2.
9%, p=0.
001) and more non-criteria events (48.
5% vs 25.
7%, p=0.
002).
Among non-criteria events, there was a higher frequency of Sneddon syndrome in triple-positive patients (7.
4% vs 0.
7%, p=0.
028).
The relapse rate was higher in triple-positive patients than in others (63.
2% vs 39,7%, p=0002).
In multivariate analysis, the triple-positive profile was associated with a higher risk of relapse (HR 1.
63; 95% CI 1.
04 to 2.
55; p=0.
031).
Conclusion
The triple-positivity is associated with a higher risk of relapse and obstetrical complications.
Related Results
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Abstract
Introduction
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease commonly affecting women of reproductive age. Its overlap with HELLP syndrome (Hemolysi...
Risk Factors and Prognosis Analysis of Patient-Specific HLA Genomic Loss Relapse Following ATG-Based T-Cell-Replete Haploidentical Hematopoietic Stem Cell Transplantation
Risk Factors and Prognosis Analysis of Patient-Specific HLA Genomic Loss Relapse Following ATG-Based T-Cell-Replete Haploidentical Hematopoietic Stem Cell Transplantation
Abstract
Background
Developments in related haploidentical hematopoietic stem cell transplantation (haplo-HSCT) have made two immune systems with inco...
Clonal Evolution of Acute Myeloid Leukemia Following Allogeneic Stem Cell Transplantation
Clonal Evolution of Acute Myeloid Leukemia Following Allogeneic Stem Cell Transplantation
Abstract
The evolutionary model of cancer progression suggests that malignant clones survive initial therapy and acquire new mutations, ultimately resulting in thera...
Targeting Genomic Heterogeneity of Adult Acute Lymphoblastic Leukemia
Targeting Genomic Heterogeneity of Adult Acute Lymphoblastic Leukemia
Abstract
Introduction: In acute lymphoblastic leukemia (ALL) genetic diversity at diagnosis has been reported to be correlated with an increased likelihood of emergi...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract
Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...
Time to Relapse and Its Predictors among Children with Nephrotic Syndrome in Comprehensive Specialized Hospitals, Tigray, Ethiopia, 2019
Time to Relapse and Its Predictors among Children with Nephrotic Syndrome in Comprehensive Specialized Hospitals, Tigray, Ethiopia, 2019
Background. Relapse in children with nephrotic syndrome leads to a variety of complications due to prolonged treatment and potential dependency on steroids. However, there is no st...
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Abstarct
Introduction
Isolated brain hydatid disease (BHD) is an extremely rare form of echinococcosis. A prompt and timely diagnosis is a crucial step in disease management. This ...
Surfactant system of the lungs in antiphospholipid syndrome under the conditions of administration of the immunosuppressive agent FTY-720
Surfactant system of the lungs in antiphospholipid syndrome under the conditions of administration of the immunosuppressive agent FTY-720
Antiphospholipid syndrome (APS) is a thrombophilic disease in the pathogenesis of which the leading role belongs to antibodies reacting with antigenic determinants of phospholipids...

