Quantitative genetics of circulating Hyaluronic Acid (HA) and its correlation with hand osteoarthritis and obesity-related phenotypes in a community-based sample

被引:7
作者
Prakash, Jai [1 ]
Gabdulina, Gulzhan [2 ]
Trofimov, Svetlana [1 ]
Livshits, Gregory [1 ,3 ]
机构
[1] Tel Aviv Univ, Dept Anat & Anthropol, Human Populat Biol Res Unit, Tel Aviv, Israel
[2] Asfendiyarov Kazakh Natl Med Univ, Dept Internal Med, Almigty, Kazakhstan
[3] Tel Aviv Univ, Sackler Fac Med, Lilian & Marcel Pollak Chair Biol Anthropol, Tel Aviv, Israel
基金
以色列科学基金会;
关键词
HA; Kellgren-Lawrence; joint space narrowing; adiponectin; leptin; fat mass; sarcopenic index; additive genetics; heritability; PREDICTING BODY DENSITY; GENERALIZED EQUATIONS; KNEE OSTEOARTHRITIS; CHRONIC PAIN; ASSOCIATION; ADIPONECTIN; HERITABILITY; PREVALENCE; LEPTIN; POLYMORPHISMS;
D O I
10.1080/03014460.2017.1334822
中图分类号
Q98 [人类学];
学科分类号
070906 [古生物学及地层学(含古人类学)];
摘要
Background: One of the potential molecular biomarkers of osteoarthritis (OA) is hyaluronic acid (HA). HA levels may be related to the severity and progression of OA. However, little is known about the contribution of major risk factors for osteoarthritis, e.g. obesity-related phenotypes and genetics to HA variation. Aim: To clarify the quantitative effect of these factors on HA. Subjects and methods: An ethnically homogeneous sample of 911 apparently healthy European-derived individuals, assessed for radiographic hand osteoarthritis (RHOA), HA, leptin, adiponectin, and several anthropometrical measures of obesity-related phenotypes was studied. Model-based quantitative genetic analysis was used to reveal genetic and shared environmental factors affecting the variation of the study's phenotypes. Results: The HA levels significantly correlated with the age, RHOA, adiponectin, obesity-related phenotypes, and the waist-to-hip ratio. The putative genetic effects contributed significantly to the variation of HA (66.2 +/- 9.3%) and they were also significant factors in the variations of all the other studied phenotypes, with the heritability estimate ranging between 0.122 +/- 4.4% (WHR) and 45.7 +/- 2.2% (joint space narrowing). Conclusions: This is the first study to report heritability estimates of HA variation and its correlation with obesity-related phenotypes, ADP and RHOA. However, the nature of genetic effects on HA and its correlation with other study phenotypes require further clarification.
引用
收藏
页码:522 / 530
页数:9
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