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1. Systemic lupus international collaborating clinics-2012 and European league against rheumatism/American college of rheumatology-2019 classification criteria for systemic lupus erythematosus associated with childhood-onset auto-immune cytopenia.

Author

Granel, Jérôme, Fernandes, Helder, Richer, Olivier, Clet, Johanna, Dubrasquet, Mathilde, Pillet, Pascal, and Aladjidi, Nathalie

Subjects
SYSTEMIC lupus erythematosus, SYMPTOMS, CYTOPENIA, RHEUMATISM, EARLY diagnosis
Abstract

Introduction: Systemic Lupus Erythematosus (SLE) can be diagnosed using the 2012 criteria of the Systemic Lupus International Collaborating Clinics (SLICC) and, more recently, the 2019 criteria of the European League Against Rheumatism/American College of Rheumatology (EULAR/ACR). Hematological involvement is scored differently by these classifications. Our objective was to compare both criteria in a cohort of children with autoimmune cytopenia (AIC)-associated SLE. Method: We included 79 patients with childhood-onset AIC as the first manifestations of SLE. Results: The median age at SLE diagnosis was 14.5 years (1.1–21.4 years). The SLICC criteria were fulfilled by 76/79 (96%) patients and the EULAR/ACR criteria by 72/79 (91%) patients during follow-up. The SLICC and EULAR/ACR criteria were discordant (not concomitantly fulfilled) in 25/79 (32%) patients. Non-hematological clinical manifestations were more frequently observed in SLE diagnosis when the criteria were concordant (30/54, 56%) than when they were not (5/25, 20%) (p = 0.004). In 16/25 (64%) discordant patients, the SLICC criteria allowed earlier diagnosis of SLE. Finally, the attribution of a maximum weight of 6 to the hematological involvement of the EULAR/ACR criteria increased the sensitivity thereof from 63/79 (80%) to 76/79 (96%) in our population. Conclusion: The SLICC 2012 and EULAR/ACR 2019 criteria do not effectively diagnose SLE in children when AIC is the predominant feature. The SLICC criteria appear to be more effective in this population of SLE patients. An increase in the maximum weight of hematological involvement to 6 increases the sensitivity of the EULAR/ACR criteria for SLE diagnosis in children. [ABSTRACT FROM AUTHOR]

Published
2024
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2. Risk of autoimmune diseases and human papilloma virus (HPV) vaccines: Six years of case-referent surveillance

Author

Abbas, Firas, Abdelmoumni, Abdelhakim, Hilliquin, Pascal, Requeda, Elisabeth, Adoue, Daniel, Brassat, David, Agard, Christian, Masseau, Agathe, Aladjidi, Nathalie, Clet, Johanna, Fernandes, Helder, Lemasson, Gwendal, Perel, Yves, Raymond, Isabelle, Richer, Olivier, Vital, Anne, Allain-Launay, Emma, Bru, Marie, Nicolino, Marc, Thomas, Caroline, Altman, Jean-Jacques, Amsallem, Daniel, Aras, Nazmiye, Boukari, Latifato, Dubrel, Marie, Fain, Olivier, Letellier, Edouard, Lucidarme, Nadine, Mekinian, Arsène, Morin, Anne-Sophie, Stirnemann, Jérôme, Atlan, Catherine, Audry, Dominique, Augustin, Jérôme, Bakir, Redouane, Bartolucci, Pablo, Chevalier, Xavier, Godeau, Bertrand, Guillaud, Constance, Khellaf, Mehdi, Limal, Nicolas, Lousteau, Valentine, Mahevas, Matthieu, Méliksetyan, Gayane, Michel, Marc, Roumier, Mathilde, Bayart, Sophie, Bonnet, Fabrice, Decaux, Olivier, Bekherraz, Amine, Brihaye, Benoit, Dachez, Roger, Daugas, Eric, Hayem, Gilles, Meyer, Olivier, Papo, Thomas, Pasqualoni, Elisa, Sacre, Karim, Travert, Florence, Bellon, Hélène, Beltrand, Jacques, Lefrere, François, Simon, Albane, Benhamou, Pierre-Yves, Benveniste, Olivier, Bolgert, Francis, Costedoat-Chalumeau, Nathalie, De Paz, Raphael, Demeret, Sophie, Fautrel, Bruno, Jacqueminet, Sophie, Louapre, Céline, Maillart, Elizabeth, Morel, Nathalie, Papeix, Caroline, Rigabert, Julie, Bensaid, Philippe, Berger, Claire, Berquin, Patrick, Le Moing, Anne-Gaëlle, Berroir, Stéphane, Besson, Gérard, Boutte, Célia, Casez, Olivier, Bonnotte, Bernard, Audia, Sylvain, Bossu-Estour, Cécile, Bourgarit, Anne, Dupuy, Alain, Keshmandt, Homa, Bourre, Bertrand, Brac, Aude, Perrin, Agnès, Pondarré, Corinne, Villar-Fimbel, Sylvie, Bruckert, Isabelle, Cosson, Anne, Magy-Bertrand, Nadine, Tisserand, Guillaume, Camu, William, Carlander, Bertrand, Morales, Raul Juntas, Cances, Claude, Pasquet, Marlene, Castilla Lievre, Maria Angela, Chabroux, Stephanie, Charif, Mamoud, Chatelus, Emmanuel, Sibilia, Jean, Chevrant-Breton, Jacqueline, Clavel, Sylvaine, Bille-Turc, Françoise, Cohen, Jacques, Courcoux, Marie France, Leverger, Guy, Machet, Laurent, Cuisset, Jean-Marie, Cony-Makhoul, Pascale, Darsy, Paul, Favre, Sandrine, Giraud, Pierrick, Leitenschenck, Laurence, Monteiro, Irène, Morati, Chafika, DeSeze, Jérôme, Dinulescu, Monica, Dhaoui, Taher, Dommange-Romero, Florence, Drevard, Elisabeth, Dupuis, Clémentine, Dumuis, Marie-Laure, Durand, Jean-Marc, Farad, Samia, Lecomte, Pierre, Pierre, Peggy, Fouyssac, Fanny, Gaudin, Philippe, Gautier, Alain, Gellen-Dautremer, Justine, Jarrin, Irène, Richette, Pascal, Georget, Emilie, Gras, Pierre, Moreau, Thibault, Giraud, Eric, Hacini, Maya, Mayer, Anne, Guillaumat, Cécile, Guillaume, Séverine, Guitton, Corinne, Kone-Paut, Isabelle, Marsaud, Céline, Rossi, Linda, Guyot, Marie-Hélène, Hassler, Patrick, Heimfert, Claude, Heinzlef, Olivier, Hillion, Brigitte, Hocquelet, Catherine, Husson, Helene, Ichai, Pierre, Jeziorski, Eric, Deslandre, Chantal Job, Le Guern, Véronique, Kamenov, Kamen, Kerlan, Véronique, Lemoine, Philippe, Misery, Laurent, Pan-Petesch, Brigitte, Krivitzky, Alain, Labauge, Pierre, Rodier, Michel, Lacade, Chadi, Razafimahefa, Berthe, Lachgar, Karim, Larmarau, Marie-Pierre, Leblanc, Thierry, Lebrun-Frenay, Christine, Lefèbvre, Patrick, Lejoyeux, Philippe, Leske, Charles, Ly, Kim, Magy, Laurent, Mansuy, Sylvie, Marechaud, Richard, Martin Negrier, Marie-Laure, Sole, Guilhem, Maupetit, Jean, Mazingue, Françoise, Mochon, Stéphanie, Moktar, Blidi, Morcamp, Donald, Morlet-Barla, Nathalie, Nicolas, Guillaume, Pautot, Vivien, Pellier, Isabelle, Verret, Jean-Luc, Outteryck, Olivier, Vermersch, Patrick, Pallot-Prades, Beatrice, Paquet, Jean Michel, Puechal, Xavier, Sortais, Annie, Pelletier, Jean, Rico, Audrey, Pez, Dominique, Stankoff, Bruno, Quittet, Philippe, Rémy, Claude, Roba, Eléna, Rosario, Hélène, Roudaut, Nathalie, Sonnet, Emmanuel, Ruel, Michel, Sebban, Samuel, Schaepelynck, Pauline, Simonin, Marie-Jeanne, Vial, Christophe, Viallard, Jean-Francois, Ladedan, Isabelle, Zenone, Thierry, Grimaldi-Bensouda, Lamiae, Rossignol, Michel, Koné-Paut, Isabelle, Courcoux, Marie-France, Viallard, Jean-François, Bourgault-Villada, Isabelle, Breart, Gerard, and Abenhaim, Lucien

Published
2017
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6. Risk of autoimmune diseases and human papilloma virus (HPV) vaccines: Six years of case-referent surveillance

Author

Grimaldi-Bensouda, Lamiae, primary, Rossignol, Michel, additional, Koné-Paut, Isabelle, additional, Krivitzky, Alain, additional, Lebrun-Frenay, Christine, additional, Clet, Johanna, additional, Brassat, David, additional, Papeix, Caroline, additional, Nicolino, Marc, additional, Benhamou, Pierre-Yves, additional, Fain, Olivier, additional, Costedoat-Chalumeau, Nathalie, additional, Courcoux, Marie-France, additional, Viallard, Jean-François, additional, Godeau, Bertrand, additional, Papo, Thomas, additional, Vermersch, Patrick, additional, Bourgault-Villada, Isabelle, additional, Breart, Gerard, additional, Abenhaim, Lucien, additional, Abbas, Firas, additional, Abdelmoumni, Abdelhakim, additional, Hilliquin, Pascal, additional, Requeda, Elisabeth, additional, Adoue, Daniel, additional, Agard, Christian, additional, Masseau, Agathe, additional, Aladjidi, Nathalie, additional, Fernandes, Helder, additional, Lemasson, Gwendal, additional, Perel, Yves, additional, Raymond, Isabelle, additional, Richer, Olivier, additional, Vital, Anne, additional, Allain-Launay, Emma, additional, Bru, Marie, additional, Thomas, Caroline, additional, Altman, Jean-Jacques, additional, Amsallem, Daniel, additional, Aras, Nazmiye, additional, Boukari, Latifato, additional, Dubrel, Marie, additional, Letellier, Edouard, additional, Lucidarme, Nadine, additional, Mekinian, Arsène, additional, Morin, Anne-Sophie, additional, Stirnemann, Jérôme, additional, Atlan, Catherine, additional, Audry, Dominique, additional, Augustin, Jérôme, additional, Bakir, Redouane, additional, Bartolucci, Pablo, additional, Chevalier, Xavier, additional, Guillaud, Constance, additional, Khellaf, Mehdi, additional, Limal, Nicolas, additional, Lousteau, Valentine, additional, Mahevas, Matthieu, additional, Méliksetyan, Gayane, additional, Michel, Marc, additional, Roumier, Mathilde, additional, Bayart, Sophie, additional, Bonnet, Fabrice, additional, Decaux, Olivier, additional, Bekherraz, Amine, additional, Brihaye, Benoit, additional, Dachez, Roger, additional, Daugas, Eric, additional, Hayem, Gilles, additional, Meyer, Olivier, additional, Pasqualoni, Elisa, additional, Sacre, Karim, additional, Travert, Florence, additional, Bellon, Hélène, additional, Beltrand, Jacques, additional, Lefrere, François, additional, Simon, Albane, additional, Benveniste, Olivier, additional, Bolgert, Francis, additional, De Paz, Raphael, additional, Demeret, Sophie, additional, Fautrel, Bruno, additional, Jacqueminet, Sophie, additional, Louapre, Céline, additional, Maillart, Elizabeth, additional, Morel, Nathalie, additional, Rigabert, Julie, additional, Bensaid, Philippe, additional, Berger, Claire, additional, Berquin, Patrick, additional, Le Moing, Anne-Gaëlle, additional, Berroir, Stéphane, additional, Besson, Gérard, additional, Boutte, Célia, additional, Casez, Olivier, additional, Bonnotte, Bernard, additional, Audia, Sylvain, additional, Bossu-Estour, Cécile, additional, Bourgarit, Anne, additional, Dupuy, Alain, additional, Keshmandt, Homa, additional, Bourre, Bertrand, additional, Brac, Aude, additional, Perrin, Agnès, additional, Pondarré, Corinne, additional, Villar-Fimbel, Sylvie, additional, Bruckert, Isabelle, additional, Cosson, Anne, additional, Magy-Bertrand, Nadine, additional, Tisserand, Guillaume, additional, Camu, William, additional, Carlander, Bertrand, additional, Morales, Raul Juntas, additional, Cances, Claude, additional, Pasquet, Marlene, additional, Castilla Lievre, Maria Angela, additional, Chabroux, Stephanie, additional, Charif, Mamoud, additional, Chatelus, Emmanuel, additional, Sibilia, Jean, additional, Chevrant-Breton, Jacqueline, additional, Clavel, Sylvaine, additional, Bille-Turc, Françoise, additional, Cohen, Jacques, additional, Courcoux, Marie France, additional, Leverger, Guy, additional, Machet, Laurent, additional, Cuisset, Jean-Marie, additional, Cony-Makhoul, Pascale, additional, Darsy, Paul, additional, Favre, Sandrine, additional, Giraud, Pierrick, additional, Leitenschenck, Laurence, additional, Monteiro, Irène, additional, Morati, Chafika, additional, DeSeze, Jérôme, additional, Dinulescu, Monica, additional, Dhaoui, Taher, additional, Dommange-Romero, Florence, additional, Drevard, Elisabeth, additional, Dupuis, Clémentine, additional, Dumuis, Marie-Laure, additional, Durand, Jean-Marc, additional, Farad, Samia, additional, Lecomte, Pierre, additional, Pierre, Peggy, additional, Fouyssac, Fanny, additional, Gaudin, Philippe, additional, Gautier, Alain, additional, Gellen-Dautremer, Justine, additional, Jarrin, Irène, additional, Richette, Pascal, additional, Georget, Emilie, additional, Gras, Pierre, additional, Moreau, Thibault, additional, Giraud, Eric, additional, Hacini, Maya, additional, Mayer, Anne, additional, Guillaumat, Cécile, additional, Guillaume, Séverine, additional, Guitton, Corinne, additional, Kone-Paut, Isabelle, additional, Marsaud, Céline, additional, Rossi, Linda, additional, Guyot, Marie-Hélène, additional, Hassler, Patrick, additional, Heimfert, Claude, additional, Heinzlef, Olivier, additional, Hillion, Brigitte, additional, Hocquelet, Catherine, additional, Husson, Helene, additional, Ichai, Pierre, additional, Jeziorski, Eric, additional, Deslandre, Chantal Job, additional, Le Guern, Véronique, additional, Kamenov, Kamen, additional, Kerlan, Véronique, additional, Lemoine, Philippe, additional, Misery, Laurent, additional, Pan-Petesch, Brigitte, additional, Labauge, Pierre, additional, Rodier, Michel, additional, Lacade, Chadi, additional, Razafimahefa, Berthe, additional, Lachgar, Karim, additional, Larmarau, Marie-Pierre, additional, Leblanc, Thierry, additional, Lefèbvre, Patrick, additional, Lejoyeux, Philippe, additional, Leske, Charles, additional, Ly, Kim, additional, Magy, Laurent, additional, Mansuy, Sylvie, additional, Marechaud, Richard, additional, Martin Negrier, Marie-Laure, additional, Sole, Guilhem, additional, Maupetit, Jean, additional, Mazingue, Françoise, additional, Mochon, Stéphanie, additional, Moktar, Blidi, additional, Morcamp, Donald, additional, Morlet-Barla, Nathalie, additional, Nicolas, Guillaume, additional, Pautot, Vivien, additional, Pellier, Isabelle, additional, Verret, Jean-Luc, additional, Outteryck, Olivier, additional, Pallot-Prades, Beatrice, additional, Paquet, Jean Michel, additional, Puechal, Xavier, additional, Sortais, Annie, additional, Pelletier, Jean, additional, Rico, Audrey, additional, Pez, Dominique, additional, Stankoff, Bruno, additional, Quittet, Philippe, additional, Rémy, Claude, additional, Roba, Eléna, additional, Rosario, Hélène, additional, Roudaut, Nathalie, additional, Sonnet, Emmanuel, additional, Ruel, Michel, additional, Sebban, Samuel, additional, Schaepelynck, Pauline, additional, Simonin, Marie-Jeanne, additional, Vial, Christophe, additional, Viallard, Jean-Francois, additional, Ladedan, Isabelle, additional, and Zenone, Thierry, additional

Published
2017
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7. PFAPA syndrome is not a sporadic disease

Author

Cochard, Marie, Clet, Johanna, Le, Lan, Pillet, Pascal, Onrubia, Xavier, Guéron, Thierry, Faouzi, Mohammed, Hofer, Michaël, Cochard, Marie, Clet, Johanna, Le, Lan, Pillet, Pascal, Onrubia, Xavier, Guéron, Thierry, Faouzi, Mohammed, and Hofer, Michaël

Abstract

Objectives. To determine whether PFAPA (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis) patients have a positive family history (FH) for recurrent fever syndromes. Method. For all patients with PFAPA seen in two paediatric rheumatology centres (Romandy, Switzerland and Bordeaux, France), parents were interviewed to record the FH for periodic fever. As controls, we interviewed a group of children without history of recurrent fever. Results. We recruited 84 patients with PFAPA and 47 healthy children. The FH for recurrent fever (without an infectious cause and recurring for at least half a year) was positive in 38/84 (45%), and was positive for PFAPA (diagnosis confirmed by a physician) in 10/84 (12%) of the PFAPA patients. For 29 of the 38 patients with positive FH, the affected person was a sibling or a parent. None of the healthy children had a positive FH for recurrent fever or PFAPA. A positive FH for rheumatological diseases was seen in both groups of children. Conclusion. These data show that a significant percentage of PFAPA patients present a positive FH of recurrent fever and PFAPA. This familial susceptibility suggests a potential genetic origin for this syndrome

Published
2017

8. PFAPA syndrome is not a sporadic disease

Author

Cochard, Marie, Clet, Johanna, Le, Lan, Pillet, Pascal, Onrubia, Xavier, Guéron, Thierry, Faouzi, Mohammed, Hofer, Michaël, Cochard, Marie, Clet, Johanna, Le, Lan, Pillet, Pascal, Onrubia, Xavier, Guéron, Thierry, Faouzi, Mohammed, and Hofer, Michaël

Abstract

Objectives. To determine whether PFAPA (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis) patients have a positive family history (FH) for recurrent fever syndromes. Method. For all patients with PFAPA seen in two paediatric rheumatology centres (Romandy, Switzerland and Bordeaux, France), parents were interviewed to record the FH for periodic fever. As controls, we interviewed a group of children without history of recurrent fever. Results. We recruited 84 patients with PFAPA and 47 healthy children. The FH for recurrent fever (without an infectious cause and recurring for at least half a year) was positive in 38/84 (45%), and was positive for PFAPA (diagnosis confirmed by a physician) in 10/84 (12%) of the PFAPA patients. For 29 of the 38 patients with positive FH, the affected person was a sibling or a parent. None of the healthy children had a positive FH for recurrent fever or PFAPA. A positive FH for rheumatological diseases was seen in both groups of children. Conclusion. These data show that a significant percentage of PFAPA patients present a positive FH of recurrent fever and PFAPA. This familial susceptibility suggests a potential genetic origin for this syndrome

9. Anakinra as a first-line therapy for systemic juvenile idiopathic arthritis when nonsteroidal anti-inflammatory drug treatment fails: A single-center French retrospective study.

Author

Granel J, Ravalet A, Daghistani A, Clet J, Richer O, Bailhache M, and Pillet P

Subjects
Humans, Child, Male, Retrospective Studies, Female, Child, Preschool, Adolescent, Infant, France, Treatment Outcome, Arthritis, Juvenile drug therapy, Interleukin 1 Receptor Antagonist Protein therapeutic use, Antirheumatic Agents therapeutic use, Antirheumatic Agents administration & dosage, Anti-Inflammatory Agents, Non-Steroidal therapeutic use, Anti-Inflammatory Agents, Non-Steroidal administration & dosage, Treatment Failure
Abstract

Introduction: Anakinra has dramatically improved the management of systemic juvenile idiopathic arthritis (SJIA) over the last decade. Nevertheless, management remains inconsistent; corticosteroids are still frequently used. We analyzed the course of SJIA in children treated with anakinra according to the time of treatment initiation after disease onset., Method: Children with SJIA treated with anakinra between 2006 and 2020 were included in this single-center, retrospective observational study., Results: Twenty-four children received anakinra at a median time of 58 (range 12-2940) days after SJIA onset, all after failure of nonsteroidal anti-inflammatory drug (NSAID) treatment. Eighteen were males and the median age at disease onset was 6.04 (range 0.8-13) years. The median follow-up time was 3.5 (range 0.5-10.8) years after treatment initiation. At the last follow-up, remission attributable to anakinra was observed in 18/24 (75%) children and treatment-free remission was observed in 12 (67%). For each child, the response to anakinra was the same at 3 months and at the last follow-up. The 15 children treated with anakinra within the first 3 months after disease onset exhibited better remission (93%) than did the 9 children treated after 3 months (44%) (p = 0.015) and the former received fewer corticosteroids (7% versus 67%) (p = 0.004). One child with long-standing disease died of the disease., Conclusions: Early anakinra initiation within the first 3 months of SJIA onset after NSAID failure ensures long-term remission and reduces corticosteroid use. Anakinra should not be continued for more than 3 months in nonresponding children.

Published
2024
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