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Development of clinical and laboratory biomarkers in an international cohort of 428 children with lupus nephritis.
De Mutiis, Chiara; Wenderfer, Scott E; Basu, Biswanath; Bagga, Arvind; Orjuela, Alvaro; Sar, Tanmoy; Aggarwal, Amita; Jain, Avinash; Boyer, Olivia; Yap, Hui-Kim; Ito, Shuichi; Ohnishi, Ai; Iwata, Naomi; Kasapcopur, Ozgur; Laurent, Audrey; Chan, Eugene Yu-Hin; Mastrangelo, Antonio; Ogura, Masao; Shima, Yuko; Rianthavorn, Pornpimol; Silva, Clovis A; Trindade, Vitor; Tullus, Kjell.
Afiliação
  • De Mutiis C; Paediatric Unit, Maggiore Hospital, Azienda USL, Bologna, Italy. chiarademutiis@yahoo.com.
  • Wenderfer SE; Pediatric Nephrology, The University of British Columbia, BC Children's Hospital, Vancouver, BC, Canada.
  • Basu B; Division of Pediatric Nephrology, Department of Pediatrics, Nilratan Sircar Medical College and Hospital, Kolkata, India.
  • Bagga A; Division of Nephrology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Orjuela A; Pediatric Nephrology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, USA.
  • Sar T; Division of Pediatric Nephrology, Department of Pediatrics, Nilratan Sircar Medical College and Hospital, Kolkata, India.
  • Aggarwal A; Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
  • Jain A; Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
  • Boyer O; Department of Clinical Immunology and Rheumatology, Sawai Mansingh Medical College, Jaipur, India.
  • Yap HK; Pediatric Nephrology, Necker Enfants Malades Hospital, Université Paris Cité, Paris, France.
  • Ito S; Néphrologie Pédiatrique, Hôpital Necker, Paris, France.
  • Ohnishi A; Department of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Iwata N; Department of Pediatrics, Yokohama City University, Fukuura, Kanazawa-Ku, Yokohama, Kanagawa, Japan.
  • Kasapcopur O; Department of Pediatrics, Yokohama City University, Fukuura, Kanazawa-Ku, Yokohama, Kanagawa, Japan.
  • Laurent A; Department of Infection and Immunology, Aichi Children's Health and Medical Center, Obu, Japan.
  • Chan EY; Department of Pediatric Rheumatology, Istanbul University-Cerrahpasa, Cerrahpasa Medical Faculty, Istanbul, Turkey.
  • Mastrangelo A; Department of Pediatric Nephrology, Rheumatology and Dermatology, Hospices Civils de Lyon, Lyon, France.
  • Ogura M; Paediatric Nephrology Centre, Hong Kong Children's Hospital, Kowloon, Hong Kong SAR.
  • Shima Y; Department of Paediatrics, The Chinese University of Hong Kong, Shatin, Hong Kong SAR.
  • Rianthavorn P; Pediatric Nephrology, Dialysis and Transplant Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
  • Silva CA; Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
  • Trindade V; Department of Pediatrics, Wakayama Medical University, Wakayama, Japan.
  • Tullus K; Division of Nephrology, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Pediatr Nephrol ; 2024 May 28.
Article em En | MEDLINE | ID: mdl-38802607
ABSTRACT

BACKGROUND:

Lupus nephritis (LN) is a very severe manifestation of lupus. There is no consensus on which treatment goals should be achieved to protect kidney function in children with LN.

METHODS:

We retrospectively analyzed trends of commonly used laboratory biomarkers of 428 patients (≤ 18 years old) with biopsy-proven LN class ≥ III. We compared data of patients who developed stable kidney remission from 6 to 24 months with those who did not.

RESULTS:

Twenty-five percent of patients maintained kidney stable remission while 75% did not. More patients with stable kidney remission showed normal hemoglobin and erythrocyte sedimentation rate from 6 to 24 months compared to the group without stable kidney remission. eGFR ≥ 90 ml/min/1.73m2 at onset predicted the development of stable kidney remission (93.8%) compared to 64.7% in those without stable remission (P < 0.00001). At diagnosis, 5.9% and 20.2% of the patients showed no proteinuria in the group with and without stable kidney remission, respectively (P = 0.0001). dsDNA antibodies decreased from onset of treatment mainly during the first 3 months in all groups, but more than 50% of all patients in both groups never normalized after 6 months. Complement C3 and C4 increased mainly in the first 3 months in all patients without any significant difference.

CONCLUSIONS:

Normal eGFR and the absence of proteinuria at onset were predictors of stable kidney remission. Significantly more children showed normal levels of Hb and erythrocyte sedimentation rate (ESR) from 6 to 24 months in the group with stable kidney remission.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article