Abstract
BACKGROUND: Vascular endothelial growth factor-A(165) (VEGF-A(165)) has been identified as a combination of 2 alternative splice variants: proangiogenic VEGF-A(165)a and antiangiogenic VEGF-A(165)b. Intracranial atherosclerotic disease (ICAD) and moyamoya disease (MMD) are 2 main types of intracranial arterial steno-occlusive disorders with distinct capacities for collateral formation. Recent studies indicate that VEGF-A(165) regulates collateral growth in ischemia. Therefore, we investigated if there is a distinctive composition of VEGF-A(165) isoforms in ICAD and MMD. METHODS: Sixty-six ICAD patients, 6 MMD patients, and 5 controls were enrolled in this prospective study. ICAD and MMD patients received intensive medical management upon enrollment. Surgery was offered to 9 ICAD patients who had recurrent ischemic events, 6 MMD patients, and 5 surgical controls without ICAD. VEGF-A(165)a and VEGF-A(165)b plasma levels were measured at baseline, within 1 week after patients having surgery, and at 1, 3, and 6 months after treatment. RESULTS: A significantly higher baseline VEGF-A(165)a/b ratio was observed in MMD compared to ICAD (P = .016). The VEGF-A(165)a/b ratio increased significantly and rapidly after surgical treatment in ICAD (P = .026) more so than in MMD and surgical controls. In patients with ICAD receiving intensive medical management, there was also an elevation of the VEGF-A(165)a/b ratio, but at a slower rate, reaching the peak at 3 months after initiation of treatment (baseline versus 3 months VEGF-A(165)a/b ratio, P = .028). CONCLUSIONS: Our study shows an increased VEGF-A(165)a/b ratio in MMD compared to ICAD, and suggests that both intensive medical management and surgical revascularization elevate the VEGF-A(165)a/b ratio in ICAD patients.