Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head

<i>Background and objectives</i>: Alterations in mitochondrial DNA (mtDNA) have been observed and studied in various diseases. However, the clinical value of the mtDNA copy number (mtDNA-CN) alterations in osteonecrosis of the femoral head (ONFH) is poorly understood. In the present stud...

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Main Authors: Si-Wook Lee, Kyung-Jae Lee, Beom-Soo Kim, Hyuk-Jun Kwon, Jae-Ho Lee
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Medicina
Subjects:
Online Access:https://www.mdpi.com/1010-660X/56/5/239
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author Si-Wook Lee
Kyung-Jae Lee
Beom-Soo Kim
Hyuk-Jun Kwon
Jae-Ho Lee
author_facet Si-Wook Lee
Kyung-Jae Lee
Beom-Soo Kim
Hyuk-Jun Kwon
Jae-Ho Lee
author_sort Si-Wook Lee
collection DOAJ
description <i>Background and objectives</i>: Alterations in mitochondrial DNA (mtDNA) have been observed and studied in various diseases. However, the clinical value of the mtDNA copy number (mtDNA-CN) alterations in osteonecrosis of the femoral head (ONFH) is poorly understood. In the present study, we investigated whether alterations in mtDNA-CNs are associated with clinicopathological parameters in ONFH. <i>Materials and methods</i>: MtDNA-CNs in the synovial tissue of 34 patients with ONFH and 123 control tissues (femoral neck fracture) were measured using quantitative real-time PCR. The present study then analyzed the correlation between the mtDNA-CN and the clinicopathological characteristics of ONFH and fracture patients. <i>Results</i>: The average mtDNA-CN (mean ± standard deviation) was 23.82 ± 22.37 and 25.04 ± 24.27 in ONFH and control tissues, respectively, and was not significantly different between the groups (<i>p</i> = 0.792). The mtDNA-CN was positively associated with age (27.7% vs. 45.9%, <i>p</i> = 0.018) and negatively associated with the erythrocyte sedimentation rate (ESR) (11.8% vs. 39.7%, <i>p</i> = 0.024) in all of the samples. The study also found further associations with age (22.2% vs. 68.8%, <i>p</i> = 0.014), gender (30.0% vs. 64.3%, <i>p</i> = 0.048), and ESR (0% vs. 57.7%, <i>p</i> = 0.043) in ONFH. <i>Conclusions</i>: in this study, we demonstrated that mtDNA-CN might be a significant marker for predicting clinical characteristics in ONFH.
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spelling doaj.art-9db7db2123794acca44eaf73ca7108822023-09-02T14:27:15ZengMDPI AGMedicina1010-660X2020-05-015623923910.3390/medicina56050239Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral HeadSi-Wook Lee0Kyung-Jae Lee1Beom-Soo Kim2Hyuk-Jun Kwon3Jae-Ho Lee4Department of Orthopaedic Surgery, Keimyung University School of Medicine, Dongsan Hospital, Daegu 42601, KoreaDepartment of Orthopaedic Surgery, Keimyung University School of Medicine, Dongsan Hospital, Daegu 42601, KoreaDepartment of Orthopaedic Surgery, Keimyung University School of Medicine, Dongsan Hospital, Daegu 42601, KoreaDepartment of Orthopaedic Surgery, Keimyung University School of Medicine, Dongsan Hospital, Daegu 42601, KoreaDepartment of Anatomy, School of Medicine, Keimyung University, Daegu 42601, Korea<i>Background and objectives</i>: Alterations in mitochondrial DNA (mtDNA) have been observed and studied in various diseases. However, the clinical value of the mtDNA copy number (mtDNA-CN) alterations in osteonecrosis of the femoral head (ONFH) is poorly understood. In the present study, we investigated whether alterations in mtDNA-CNs are associated with clinicopathological parameters in ONFH. <i>Materials and methods</i>: MtDNA-CNs in the synovial tissue of 34 patients with ONFH and 123 control tissues (femoral neck fracture) were measured using quantitative real-time PCR. The present study then analyzed the correlation between the mtDNA-CN and the clinicopathological characteristics of ONFH and fracture patients. <i>Results</i>: The average mtDNA-CN (mean ± standard deviation) was 23.82 ± 22.37 and 25.04 ± 24.27 in ONFH and control tissues, respectively, and was not significantly different between the groups (<i>p</i> = 0.792). The mtDNA-CN was positively associated with age (27.7% vs. 45.9%, <i>p</i> = 0.018) and negatively associated with the erythrocyte sedimentation rate (ESR) (11.8% vs. 39.7%, <i>p</i> = 0.024) in all of the samples. The study also found further associations with age (22.2% vs. 68.8%, <i>p</i> = 0.014), gender (30.0% vs. 64.3%, <i>p</i> = 0.048), and ESR (0% vs. 57.7%, <i>p</i> = 0.043) in ONFH. <i>Conclusions</i>: in this study, we demonstrated that mtDNA-CN might be a significant marker for predicting clinical characteristics in ONFH.https://www.mdpi.com/1010-660X/56/5/239mtDNAmtDNA-CNONFHosteonecrosismitochondrial DNAESR
spellingShingle Si-Wook Lee
Kyung-Jae Lee
Beom-Soo Kim
Hyuk-Jun Kwon
Jae-Ho Lee
Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head
Medicina
mtDNA
mtDNA-CN
ONFH
osteonecrosis
mitochondrial DNA
ESR
title Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head
title_full Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head
title_fullStr Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head
title_full_unstemmed Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head
title_short Clinical Characteristics of Mitochondrial DNA Copy Number in Osteonecrosis of the Femoral Head
title_sort clinical characteristics of mitochondrial dna copy number in osteonecrosis of the femoral head
topic mtDNA
mtDNA-CN
ONFH
osteonecrosis
mitochondrial DNA
ESR
url https://www.mdpi.com/1010-660X/56/5/239
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