Your browser doesn't support javascript.
loading
Systematic review of atypical hemolytic uremic syndrome biomarkers.
Raina, Rupesh; Sethi, Sidharth K; Dragon-Durey, Marie-Agnès; Khooblall, Amrit; Sharma, Divya; Khandelwal, Priyanka; Shapiro, Ron; Boyer, Olivia; Yap, Hui Kim; Bagga, Arvind; Licht, Christoph.
Afiliación
  • Raina R; Akron Nephrology Associates/Cleveland Clinic Akron General Medical Center, Akron, OH, USA. rraina@akronchildrens.org.
  • Sethi SK; Department of Nephrology, Akron Children's Hospital, Akron, OH, USA. rraina@akronchildrens.org.
  • Dragon-Durey MA; Kidney and Renal Transplant Institute, Medanta, The Medicity Hospital, Gurgaon, Haryana, India.
  • Khooblall A; Hôpital Européen Georges Pompidou, APHP, INSERM UMRS1138, Université de Paris, Paris, France.
  • Sharma D; Akron Nephrology Associates/Cleveland Clinic Akron General Medical Center, Akron, OH, USA.
  • Khandelwal P; Department of Nephrology, Akron Children's Hospital, Akron, OH, USA.
  • Shapiro R; Department of Medicine, Northeast Ohio Medical University, Rootstown, OH, USA.
  • Boyer O; Division of Nephrology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Yap HK; The Mount Sinai Hospital, New York, NY, USA.
  • Bagga A; Service de Néphrologie Pédiatrique, AP-HP, Centre de Référence de maladies rénales rares de l'enfant et de l'adulte (MARHEA), Hôpital Necker - Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.
  • Licht C; Institut Imagine, Laboratoire des maladies rénales héréditaires, INSERM UMR 1163, Université de Paris, Paris, France.
Pediatr Nephrol ; 37(7): 1479-1493, 2022 07.
Article en En | MEDLINE | ID: mdl-35118546
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Observing biomarkers that affect alternative pathway dysregulation components may be effective in obtaining a new and more rapid diagnostic portrayal of atypical hemolytic uremic syndrome. We have conducted a systematic review on the aHUS biomarkers C3, C5a, C5b-9, factor B, complement factor B, H, and I, CH50, AH50, D-dimer, as well as anti-CFH antibodies.

METHODS:

An exhaustive literature search was conducted for aHUS patient population plasma/serum, collected/reported at the onset of diagnosis. A total of 60 studies were included with the data on 837 aHUS subjects, with at least one biomarker reported.

RESULTS:

The biomarkers C3 [mean (SD) 72.1 (35.0), median 70.5 vs. reference range 75-175 mg/dl, n = 752]; CH50 [28.3 (32.1), 24.3 vs. 30-75 U/ml, n = 63]; AH50 [27.6% (30.2%), 10% vs. ≥ 46%, n = 23]; and CFB [13.1 (6.6), 12.4, vs. 15.2-42.3 mg/dl, n = 19] were lower among aHUS subjects as compared with the reference range. The biomarkers including C4 [mean (SD) 20.4 (9.5), median 20.5 vs. reference range 14-40 mg/dl, n = 343]; C4d [7.2 (6.5), 4.8 vs. ≤ 9.8 µg/ml, n = 108]; CFH [40.2 (132.3), 24.5 vs. 23.6-43.1 mg/dl, n = 123 subjects]; and CFI [8.05 (5.01), 6.55 mg/dl vs. 4.4-18.1 mg/dl, n = 38] were all observed to be within the reference range among aHUS subjects. The biomarkers C5a [mean (SD) 54.9 (32.9), median 48.8 vs. reference range 10.6-26.3 mg/dl, n = 117]; C5b-9 [466.0 (401.4), 317 (186-569.7) vs. ≤ 250 ng/ml, n = 174]; Bb [2.6 (2.1), 1.9 vs. ≤ 1.6 µg/ml, n = 77] and D-dimer [246 (65.05), 246 vs. < 2.2 ng/ml, 2, n = 2 subjects] were higher among patients with aHUS compared with the reference range.

CONCLUSION:

If a comprehensive complement profile were built using our data, aHUS would be identified by low levels of C3, CH50, AH50, and CFB along with increased levels of C5a, C5b-9, Bb, anti-CFH autoantibodies, and D-dimer. A higher resolution version of the Graphical abstract is available as Supplementary information.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome Hemolítico Urémico Atípico Tipo de estudio: Diagnostic_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome Hemolítico Urémico Atípico Tipo de estudio: Diagnostic_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos