The Value of Coenzyme Q10 Determination in Mitochondrial Patients

被引:24
|
作者
Yubero, Delia [1 ,2 ]
Allen, George [3 ]
Artuch, Rafael [1 ,2 ]
Montero, Raquel [1 ,2 ]
机构
[1] Inst Recerca St Joan de Deu, Clin Biochem & Mol Med Dept, Passeig St Joan de Deu 2, Barcelona 08950, Spain
[2] CIBERER ISCIII, Passeig St Joan de Deu 2, Barcelona 08950, Spain
[3] Royal Devon & Exeter NHS Fdn Trust, Dept Blood Sci, Exeter EX2 5DW, Devon, England
来源
JOURNAL OF CLINICAL MEDICINE | 2017年 / 6卷 / 04期
关键词
coenzyme Q(10) deficiency; mitochondrial diseases; treatment monitoring; Q DEFICIENCY; COQ(10) DEFICIENCY; NEPHROTIC SYNDROME; INTERNAL STANDARD; OXIDATIVE STRESS; MUSCLE; FIBROBLASTS; PLASMA; HPLC; CHILDREN;
D O I
10.3390/jcm6040037
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coenzyme Q(10) (CoQ) is a lipid that is ubiquitously synthesized in tissues and has a key role in mitochondrial oxidative phosphorylation. Its biochemical determination provides insight into the CoQ status of tissues and may detect CoQ deficiency that can result from either an inherited primary deficiency of CoQ metabolism or may be secondary to different genetic and environmental conditions. Rapid identification of CoQ deficiency can also allow potentially beneficial treatment to be initiated as early as possible. CoQ may be measured in different specimens, including plasma, blood mononuclear cells, platelets, urine, muscle, and cultured skin fibroblasts. Blood and urinary CoQ also have good utility for CoQ treatment monitoring.
引用
收藏
页数:10
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