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Paramacular temporal atrophy in sickle cell disease occurs early in childhood
  1. Gilles C Martin1,2,
  2. Eliane Albuisson3,4,5,
  3. Valentine Brousse6,
  4. Mariane de Montalembert6,
  5. Dominique Bremond-Gignac1,
  6. Matthieu P Robert1,2
  1. 1 Ophthalmology Department and Rare Ophthalmological Diseases Reference Centre, Necker-Enfants Malades University Hospital, APHP, Paris, France
  2. 2 Cognition and Action Group, Paris Descartes University, Sorbonne Paris Cité, Paris, France
  3. 3 BIOBASE, Pôle S²R, CHRU Nancy, Vandoeuvre-lès-Nancy, France
  4. 4 Faculté de Médecine, InSciDens, Université de Lorraine, Vandoeuvre-lès-Nancy, France
  5. 5 CNRS, Institut Elie Cartan de Lorraine, UMR 7502, Vandoeuvre-lès-Nancy, France
  6. 6 Pediatry Department, Necker-Enfants Malades University Hospital, APHP, Paris, France
  1. Correspondence to Dr Gilles C Martin, Ophthalmology Department, Necker-Enfants Malades University Hospital, APHP, Paris 75015, France; gilles.martin{at}


Background/aims Initially reported in a few patients with homozygous sickle cell disease (SCD), atrophic areas of the retina temporal from the macula are now known to be present in about 48% of eyes of adult patients with SS-SCD and in 35% of eyes of adult patients with SC-SCD. The aim of this study is to describe this paramacular atrophy in children affected with SCD.

Methods In this retrospective series, spectral-domain optical coherence tomography images of 81 children with SCD, acquired with specific patterns including one evaluating the retina temporal to the macula, were reviewed, in order to look for retinal atrophy. Fundus examination status for SCD peripheral retinopathy was also reviewed.

Results Mean age was 12.0 years (SD: 3.56). The genotype distribution was: 64 HbSS (79%), 10 HbSC (12%) and 7 HbS/β0 thalassaemia (9%). Using a usual fovea-centred programme, retinal atrophy was found in 38% of eyes (52% of children). Using a specific temporal pattern, retinal atrophy was found in 53% of eyes (64% of children), with no significant difference in the prevalence between HbSS and HbSC genotype (p=0.92), and no effect of age (mean 12.3 years (SD=3.61) vs11.9 (3.56), p=0.65). Peripheral retinopathy was found in 11% of children, with a significant relation between the HbSC genotype and the severity of the retinopathy (p=0.003).

Conclusion Paramacular temporal atrophy occurs early in the course of SCD, which suggests distinct mechanisms from those of peripheral retinopathy.

  • child health (paediatrics)
  • macula
  • retina

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  • Contributors GCM, EA, VB, MdM, DB-G and MPR all meet the criteria for authorship, having taken part in the conception or design of the work, or the acquisition, analysis or interpretation of data; having drafted the work or revised it critically for important intellectual content; having approved the version published; and giving full agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

  • Funding GCM has received a funding from the Fondation pour la Recherche Médicale (DEA20150633354).

  • Competing interests None declared.

  • Patient consent Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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