期刊
JOURNAL OF CLINICAL MEDICINE
卷 12, 期 2, 页码 -出版社
MDPI
DOI: 10.3390/jcm12020483
关键词
homozygous familial hypercholesterolemia; severe heterozygous familial hypercholesterolemia; metabolomics; diagnostic markers
This study discovered a unique metabolic pattern for screening homozygotes in patients with severe familial hypercholesterolemia (FH) through metabolomic profiling. By using this cost-effective method, homozygotes can be preselected in FH patients, allowing clinicians to conduct selective genetic confirmation testing and familial cascade screening.
Homozygous familial hypercholesterolemia (HoFH) is a rare inborn-errors-of-metabolism disorder characterized by devastatingly elevated low-density lipoprotein cholesterol (LDL-C) and premature cardiovascular disease. The gold standard for screening and diagnosing HoFH is genetic testing. In China, it is expensive and is always recommended for the most likely HoFH subjects with aggressive LDL-C phenotype. However, the LDL-C levels of HoFH patients and a substantial proportion of heterozygous FH (HeFH) patients overlapped considerably. Here, we performed a cost-effective metabolomic profiling on genetically diagnosed HoFH (n = 69) and HeFH patients (n = 101) with overlapping LDL-C levels, aiming to discovery a unique metabolic pattern for screening homozygotes in patients with severe FH. We demonstrated a differential serum metabolome profile in HoFH patients compared to HeFH patients. Twenty-one metabolomic alterations showed independent capability in differentiating HoFH from severe HeFH. The combined model based on seven identified metabolites yielded a corrected diagnosis in 91.3% of HoFH cases with an area under the curve value of 0.939. Collectively, this study demonstrated that metabolomic profiling serves as a useful and economical approach to preselecting homozygotes in FH patients with severe hypercholesterolemia and may help clinicians to conduct selective genetic confirmation testing and familial cascade screening.
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