BACKGROUND: Lumbar disc disease (LDD), one of the most common conditions for which patients seek medical care, has been associated with sequence changes of the COL genes. COL1A1, however, has not been studied in young patients with LDD; COL1A1 polymorphisms have been associated with bone mineral density (BMD) in several populations and with LDD in older adults. OBJECTIVE: To study COL1A1 polymorphisms in young Greek army recruits with LDD. SUBJECTS: These young soldiers were diagnosed with early LDD at the time of their presentation to a military training site. All patients had radiological confirmation of their disease; a control group was also studied. METHODS: Sp1-binding site polymorphism of the COL1A1 gene was investigated by standard methods. RESULTS: There was an increased frequency of the "ss" genotype (33.3%) in LDD patients; none of the controls had this genotype. In addition, a significantly smaller number of controls was heterozygotes for this allele. CONCLUSIONS: A previously studied sequence change of the regulatory region of the COL1A1 gene, the same as has previously been associated with low BMD in many populations and LDD in older adults, showed a strong association with LDD in young male soldiers who were recently diagnosed with this disease.
BACKGROUND:Lumbar disc disease (LDD), one of the most common conditions for which patients seek medical care, has been associated with sequence changes of the COL genes. COL1A1, however, has not been studied in young patients with LDD; COL1A1 polymorphisms have been associated with bone mineral density (BMD) in several populations and with LDD in older adults. OBJECTIVE: To study COL1A1 polymorphisms in young Greek army recruits with LDD. SUBJECTS: These young soldiers were diagnosed with early LDD at the time of their presentation to a military training site. All patients had radiological confirmation of their disease; a control group was also studied. METHODS: Sp1-binding site polymorphism of the COL1A1 gene was investigated by standard methods. RESULTS: There was an increased frequency of the "ss" genotype (33.3%) in LDDpatients; none of the controls had this genotype. In addition, a significantly smaller number of controls was heterozygotes for this allele. CONCLUSIONS: A previously studied sequence change of the regulatory region of the COL1A1 gene, the same as has previously been associated with low BMD in many populations and LDD in older adults, showed a strong association with LDD in young male soldiers who were recently diagnosed with this disease.
Authors: Jillian E Mayer; James C Iatridis; Danny Chan; Sheeraz A Qureshi; Omri Gottesman; Andrew C Hecht Journal: Spine J Date: 2013-03 Impact factor: 4.166
Authors: Arseniy M Smirnov; Grigory S Demin; Marina M Mnuskina; Larisa A Scheplyagina; Mikhail M Kostik; Valentina I Larionova Journal: EPMA J Date: 2013-06-13 Impact factor: 6.543
Authors: Zafer Orkun Toktaş; Murat Şakir Ekşi; Baran Yılmaz; Mustafa Kemal Demir; Serdar Özgen; Türker Kılıç; Deniz Konya Journal: Eur Spine J Date: 2015-09-05 Impact factor: 3.134