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Published on: February 11, 2014
Visual pathway function in adults born preterm with very low birth weight: a two-country birth cohort study
Anna P M Jørgensen1, Maarit Kulmala2,3, Dordi Austeng4,5
1Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology (NTNU), 7491, Trondheim, Norway. anna.p.m.jorgensen@ntnu.no.
Insights
Adults born preterm with very low birth weight (VLBW) showed subtle visual pathway differences, including delayed cortical responses and altered macular function. These electrophysiological changes did not impact best-corrected visual acuity (BCVA).
Area of Science:
- Ophthalmology
- Neuroscience
- Developmental Biology
Background:
- Preterm birth with very low birth weight (VLBW) is a significant risk factor for adverse neurodevelopmental outcomes.
- Visual pathway development can be affected by prematurity and low birth weight, potentially leading to long-term functional deficits.
- Understanding the long-term visual function in adults born VLBW is crucial for identifying potential health risks and guiding interventions.
Purpose of the Study:
- To investigate the long-term effects of preterm birth with very low birth weight (VLBW) on macular and visual pathway function in adulthood.
- To determine if best-corrected visual acuity (BCVA) is associated with electrophysiological responses in adults born VLBW.
- To compare visual pathway function between adults born preterm with VLBW and term-born controls.
Main Methods:
- Fifty adults born preterm with VLBW and 77 term-born controls (aged 31-41 years) were recruited from Finnish and Norwegian longitudinal studies.
- Pattern reversal electroretinogram (PR-ERG) and visual evoked potential (PR-VEP) were performed to assess macular and visual pathway function.
- Key electrophysiological components (e.g., P50, N95, N75, P100, N145) and BCVA were analyzed and compared between the VLBW and control groups.
Main Results:
- Adults born preterm with VLBW exhibited a significantly longer N145 peak time (indicating delayed cortical processing) compared to controls.
- The VLBW group also showed a lower N95:P50 amplitude ratio in the PR-ERG, suggesting potential alterations in macular function.
- Despite these electrophysiological differences, BCVA was normal and similar in both groups, with no significant association found between electrophysiologic responses and BCVA.
Conclusions:
- While primary visual cortex responses (N75, P100) were comparable, subtle electrophysiological deviations at higher cortical levels (N145) and in macular function (ganglion cell response) were observed in adults born preterm with VLBW.
- These findings suggest that preterm birth with VLBW may lead to subclinical visual pathway alterations that do not manifest as reduced visual acuity in adulthood.
- Further research is warranted to understand the clinical implications and potential long-term consequences of these subtle visual pathway differences.
Purpose:
To investigate if preterm birth with very low birth weight (VLBW; birth weight < 1500 g) affects macular and visual pathway function in an adult population and explore if best corrected visual acuity (BCVA) was associated with any of the electrophysiologic responses.
Methods:
Fifty participants born preterm with VLBW and 77 term-born controls years were recruited when aged 31-41 years from the Helsinki Study of Very Low Birth Weight Adults (Finland) and the NTNU Low Birth Weight Life study (Norway) studies. Pattern reversal electroretinogram (PR-ERG), visual evoked potential (PR-VEP) and BCVA were examined. PR-ERG components (P50, N95 peak time, amplitude and N95:P50 amplitude ratio) and PR-VEP components (N75, P100 and N145 peak time and amplitude) in the better-seeing eye were compared between the groups, and association with BCVA was examined.
Results:
The VLBW group showed longer N145 peak time compared to the control group (mean difference 6.8 ms, CI 2.0 to 11.5, p = 0.006) and lower N95:P50 amplitude ratio (CI - 0.3 to - 0.1, p = 0.003). Otherwise, both groups showed similar electrophysiological waveforms. No relationship was found between electrophysiologic responses and BCVA. BCVA was normal in birth groups and showed no group difference.
Conclusion:
The responses in the primary visual cortex (N75 and P100) to visual stimuli presented to the better-seeing eye were similar in adults born preterm with VLBW and term-born controls. However, in the VLBW group, there was an indication that subtle electrophysiological deviation may exist at a higher cortical level (N145) and in the ganglion cell response in the macula. These significant differences were not related to reduced visual acuity.
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