Barnaby Amber M, Hansen Ronald M, Moskowitz Anne, Fulton Anne B
Department of Ophthalmology, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4854-60. doi: 10.1167/iovs.07-0406.
To test the hypothesis that the late-maturing parafoveal rod photoreceptors are more vulnerable than peripheral rods to the effects of retinopathy of prematurity (ROP).
Twenty-four infants with a history of preterm birth (gestational age at birth </=31 weeks) participated in a longitudinal study: 12 had mild ROP that resolved without treatment, and 12 had never had ROP. Thresholds for detecting stimuli (2 degrees diameter, 50 ms duration) presented 10 degrees (parafoveal) and 30 degrees (peripheral) from a central fixation target were estimated by using a preferential-looking
At each visit, thresholds at both sites were obtained in random order. Thresholds of the preterm subjects were compared with those of previously reported term infants.
The course of threshold maturation in subjects with ROP was significantly prolonged (P </= 0.01) compared with those who had never had ROP and with term-born control subjects. On average, parafoveal thresholds in subjects with ROP reached the adult level at a median age of 12 (range, 6-18) months, and peripheral thresholds reached the adult level at 9 (range, 5-12) months. Median thresholds in subjects who had never had ROP reached adult levels at both sites by approximately 7 months.
The slower development of parafoveal compared with peripheral thresholds in subjects with a history of ROP is evidence that the late-maturing parafoveal rods are more affected by the ROP disease process.
检验以下假设,即成熟较晚的旁中心凹视杆细胞比周边视杆细胞更容易受到早产儿视网膜病变(ROP)的影响。
24名有早产史(出生时胎龄≤31周)的婴儿参与了一项纵向研究:12名患有轻度ROP且未经治疗自行消退,12名从未患过ROP。通过优先注视法估计检测呈现于距中央固定目标10度(旁中心凹)和30度(周边)的刺激(直径2度,持续时间50毫秒)的阈值。
每次访视时,以随机顺序获取两个部位的阈值。将早产受试者的阈值与先前报道的足月儿的阈值进行比较。
与从未患过ROP的受试者以及足月出生的对照受试者相比,患ROP的受试者阈值成熟过程显著延长(P≤0.01)。平均而言,患ROP的受试者旁中心凹阈值在12(范围6 - 18)个月时达到成人水平,周边阈值在9(范围5 - 12)个月时达到成人水平。从未患过ROP的受试者在两个部位的阈值中位数在大约7个月时达到成人水平。
有ROP病史的受试者旁中心凹阈值的发育比周边阈值慢,这证明成熟较晚的旁中心凹视杆细胞受ROP疾病进程的影响更大。