Hong Yoo Rha, Kim Young Ho, Kim Soo Young, Nam Gi Yup, Cheon Hee Jong, Lee Sang Joon
Departments of *Pediatrics, and †Molecular Biology, College of Medicine, Kosin University, Busan, South Korea; ‡BNG Eye Clinic, Busan, South Korea; §Department of Ophthalmology, Institute of Medicine, College of Medicine, Kosin University, Busan, South Korea; and ¶Gongjoo St. Mary's Eye Clinic, Gongjoo City, South Korea.
Retina. 2015 Sep;35(9):1772-7. doi: 10.1097/IAE.0000000000000535.
To investigate the changes in plasma concentrations of vascular endothelial growth factor (VEGF), insulin growth factor (IGF-1), erythropoietin, pigment epithelium-derived factor, and IgG1 after bevacizumab intravitreal injection in infants with retinopathy of prematurity.
Eleven eyes from six infants who received intravitreal injection of bevacizumab were enrolled in this study. At preinjection and postinjection 1, 2, 3, 4, 5, 6, 7, and 8 weeks, 0.5 mL of blood was collected from each infant. The plasma concentrations of VEGF, insulin growth factor, erythropoietin, pigment epithelium-derived factor, and IgG1 were measured by enzyme-linked immunosorbent assay. Five patients received simultaneous bilateral bevacizumab injection; one patient received unilateral injection.
Of the infants who received intravitreal bevacizumab injection, two were males and four were females. The mean gestational age was 26 ± 2 weeks. The mean birth weight was 870 g. The mean plasma VEGF concentration before bevacizumab injection was 2.05 ± 3.00 ng/mL; plasma level decreased significantly to 0.16 ± 0.10 ng/mL and to 0.14 ± 0.14 ng/mL (P = 0.028) after 1 week and 2 weeks, respectively. Moreover, the plasma concentrations of VEGF did not return to the original level in any of the samples until 8 weeks after the injection. However, mean plasma IgG1, erythropoietin, insulin growth factor, and PEDF concentrations did not change significantly during the interval between preinjection and any other follow-up time points.
Intravitreal bevacizumab injections significantly reduce plasma VEGF concentration in infants with retinopathy of prematurity over a 7-week period.
研究玻璃体内注射贝伐单抗后早产儿视网膜病变婴儿血浆中血管内皮生长因子(VEGF)、胰岛素生长因子(IGF-1)、促红细胞生成素、色素上皮衍生因子和IgG1浓度的变化。
本研究纳入了6例接受玻璃体内注射贝伐单抗的婴儿的11只眼。在注射前以及注射后1、2、3、4、5、6、7和8周,从每个婴儿采集0.5 mL血液。采用酶联免疫吸附测定法测量VEGF、胰岛素生长因子、促红细胞生成素、色素上皮衍生因子和IgG1的血浆浓度。5例患者同时接受双侧贝伐单抗注射;1例患者接受单侧注射。
接受玻璃体内贝伐单抗注射的婴儿中,2例为男性,4例为女性。平均胎龄为26±2周。平均出生体重为870 g。贝伐单抗注射前血浆VEGF平均浓度为2.05±3.00 ng/mL;注射后1周和2周时,血浆水平分别显著降至0.16±0.10 ng/mL和0.14±0.14 ng/mL(P = 0.028)。此外,在注射后8周之前,任何样本中的VEGF血浆浓度均未恢复至初始水平。然而,在注射前与其他任何随访时间点之间的间隔期内,血浆IgG1、促红细胞生成素、胰岛素生长因子和PEDF的平均浓度均未发生显著变化。
玻璃体内注射贝伐单抗可在7周内显著降低早产儿视网膜病变婴儿的血浆VEGF浓度。