TY - JOUR T1 - BIochemical and vascular aspects of pediatric chronic fatigue syndrome AU - Kennedy G, Khan F, Hill A, Underwood C, Belch JF Y1 - 2010/09/01 N1 - 10.1001/archpediatrics.2010.157 JO - Archives of Pediatrics & Adolescent Medicine SP - 817 EP - 823 VL - 164 IS - 9 N2 - Objective  To evaluate the biochemical and vascular aspects of pediatric chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME).Design  Cross-sectional clinical study.Setting  Tayside, Scotland, United Kingdom.Participants  Twenty-five children with CFS/ME and 23 healthy children recruited from throughout the United Kingdom.Interventions  Participants underwent a full clinical examination to establish a diagnosis of CFS/ME and were asked to describe and score their CFS/ME symptoms. Biochemical markers were measured. Arterial wave reflection was estimated to assess systemic arterial stiffness.Main Outcome Measures  Markers of oxidative stress and free radicals, C-reactive protein level, white blood cell apoptosis, and arterial wave reflection.Results  Children with CFS/ME had increased oxidative stress compared with control individuals (isoprostanes: 252.30 vs 215.60 pg/mL, P = .007; vitamin C, mean [SD]: 0.84 [0.26] vs 1.15 [0.28] mg/dL, P < .001; vitamin E, 8.72 [2.39] vs 10.94 [3.46] μg/mL, P = .01) and increased white blood cell apoptosis (neutrophils: 53.7% vs 35.7%, P = .005; lymphocytes: 40.1% vs 24.6%, P = .009). Arterial stiffness variables did not differ significantly between groups (mean augmentation index, −0.57% vs −0.47%, P = .09); however, the derived variables significantly correlated with total (r = 0.543, P = .02) and low-density lipoprotein (r = 0.631, P = .004) cholesterol in patients with CFS/ME but not in controls.Conclusions  Biomedical anomalies seen in adults with CFS/ME—increased oxidative stress and increased white blood cell apoptosis—can also be observed in children with clinically diagnosed CFS/ME compared with matched controls. Unlike in their adult counterparts, however, arterial stiffness remained within the reference range in these pediatric patients. SN - 1072-4710 M3 - doi: 10.1001/archpediatrics.2010.157 UR - http://dx.doi.org/10.1001/archpediatrics.2010.157 ER -