The Journal of Pediatrics
Volume 153, Issue 5 , Pages 605-611, November 2008

Maturation of Rod Function in Preterm Infants with and without Retinopathy of Prematurity

  • Ruth Hamilton, PhD

      Affiliations

    • Department of Clinical Physics, Royal Hospital for Sick Children, and Princess Royal Maternity, Glasgow, United Kingdom
    • Department of Clinical Physics, University of Glasgow, Glasgow, United Kingdom
  • ,
  • Michael S. Bradnam, PhD

      Affiliations

    • Department of Clinical Physics, Royal Hospital for Sick Children, and Princess Royal Maternity, Glasgow, United Kingdom
    • Department of Clinical Physics, University of Glasgow, Glasgow, United Kingdom
  • ,
  • John Dudgeon, MBchB

      Affiliations

    • Ophthalmology Department, Royal Hospital for Sick Children, and Princess Royal Maternity, Glasgow, United Kingdom
  • ,
  • Helen Mactier, MD

      Affiliations

    • Department of Child Health, University of Glasgow, Glasgow, United Kingdom

Received 18 July 2007; received in revised form 15 April 2008; accepted 9 May 2008. published online 14 July 2008.

Objectives

To establish normal development of rod electroretinograms in preterm infants and to assess the effects of retinopathy of prematurity (ROP).

Study design

We measured 88 Naka-Rushton functions from 41 preterm infants at maturities from 30 to 72 weeks postmenstrual age (PMA). Outcomes (log σ, retinal sensitivity and Vmax, retinal responsivity) were compared between control (no ROP), untreated ROP, and treated ROP.

Results

In control infants, sensitivity increased by 1.5 log units from 30 to 40 weeks PMA and by a further 0.5 log units by 50 weeks PMA but was 0.5 log units less than in similarly-mature, healthy, term-born infants. Average retinal responsivity increased from 23 μV to 90 μV between 30 and 40 weeks PMA and was 35 μV greater at 40 weeks PMA than in similarly-mature term-born infants. At around 36 weeks PMA, (when onset of ROP peaks), infants with untreated ROP had average retinal sensitivity 0.2 log units lower than control infants; sensitivity was reduced further in infants treated for ROP. Retinal responsiveness did not differ between control subjects and untreated infants with ROP but was greatly reduced in infants treated for ROP.

Conclusions

Maturation of rod sensitivity appears to be slowed by preterm birth whereas maturation of rod responsivity is accelerated. ROP reduces retinal sensitivity, and treated ROP reduces both sensitivity and responsivity.

Abbreviations: ERG, Electroretinography, PMA, Postmenstrual age, ROP, Retinopathy of prematurity

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 Supported by the Royal National Institute for the Blind (grant no. 2501.2651.42).

 The authors report no conflicting interests.

 No reprints.

PII: S0022-3476(08)00409-5

doi:10.1016/j.jpeds.2008.05.018

Refers to article:

  • Retinopathy of Prematurity and the Peripheral Retina

    William V. Good
    The Journal of Pediatrics November 2008 (Vol. 153, Issue 5, Pages 591-592)

The Journal of Pediatrics
Volume 153, Issue 5 , Pages 605-611, November 2008