Coenzyme Q10 levels in Prader‐Willi syndrome: Comparison with obese and non‐obese subjects

Coenzyme Q10 (CoQ10) is an essential component of the mitochondrial respiratory chain and an important scavenger of reactive oxygen species. Low levels are found in individuals with reduced energy expenditure, cardiac and skeletal muscle dysfunction, and mitochondrial disorders, many of these manifestations are seen in individuals with Prader‐Willi syndrome (PWS). In addition, CoQ10 supplementation frequently is given to individuals with this syndrome. To determine if CoQ10 levels are decreased in PWS, we studied plasma CoQ10 levels in 16 subjects with PWS, 13 with obesity of unknown cause, and 15 subjects without obesity but of similar age and compared with body composition. Plasma CoQ10 levels were significantly decreased (P < 0.05), using several statistical approaches in subjects with PWS (0.45 ± 0.16 μg/ml), compared to subjects without obesity (0.93 ± 0.56 μg/ml), but not different from subjects with obesity (0.73 ± 0.53 μg/ml). When plasma CoQ10 was normalized relative to cholesterol, triglyceride, and creatinine levels and fat and lean mass [determined by dual energy X‐ray absorptiometry (DEXA)] in the subjects with either PWS or obesity, no significant differences were observed. However, a lower muscle mass was found in the PWS subjects. © 2003 Wiley‐Liss, Inc.

[1]  F. Dawood,et al.  Conditioned nutritional deficiencies in the cardiomyopathic hamster heart. , 2001, The Canadian journal of cardiology.

[2]  M. Butler,et al.  Prader-Willi Syndrome: Clinical and Genetic Findings. , 2000, The Endocrinologist.

[3]  D. Allen,et al.  Prader-Willi Syndrome: The Effect of Growth Hormone on Childhood Body Composition , 2000 .

[4]  U. Eiholzer,et al.  Growth Hormone Deficiency in Prader-Willi Syndrome , 2000 .

[5]  S. Dimauro Exercise intolerance and the mitochondrial respiratory chain , 1999, The Italian Journal of Neurological Sciences.

[6]  M. Butler,et al.  Genetic variants of the human obesity (OB) gene in subjects with and without Prader—Willi syndrome: comparison with body mass index and weight , 1998, Clinical genetics.

[7]  N. Oda,et al.  Effects of thyroid hormone on coenzyme Q and other free radical scavengers in rat heart muscle. , 1995, The Journal of endocrinology.

[8]  M. Butler,et al.  Prader-Willi syndrome: consensus diagnostic criteria. , 1993, Pediatrics.

[9]  I. Nonaka,et al.  Muscle coenzyme Q10 in mitochondrial encephalomyopathies , 1991, Neuromuscular Disorders.

[10]  M. Butler Prader-Willi syndrome: current understanding of cause and diagnosis. , 1990, American journal of medical genetics.

[11]  L. Packer,et al.  Simultaneous determination of tocopherols, ubiquinols, and ubiquinones in blood, plasma, tissue homogenates, and subcellular fractions. , 1986, Analytical biochemistry.

[12]  M. Butler,et al.  Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. , 1986, American journal of medical genetics.

[13]  G. Bray,et al.  The Prader‐Willi Syndrome: A Study of 40 Patients and a Review of the Literature , 1983, Medicine.

[14]  M. Castro-Magana,,et al.  Pituitary Evaluation and Growth Hormone Treatment in Prader-Willi Syndrome , 1991 .