Clinical application of human β-defensin and CD14 gene polymorphism in evaluating the status of chronic inflammation

被引:18
作者
Loo, Wings T. Y. [1 ,2 ]
Bai, Lan-jun [3 ,4 ]
Fan, Chang-bin [5 ]
Yue, Yuan [6 ,7 ]
Dou, Yi-ding [8 ]
Wang, Min [6 ,7 ]
Liang, Hao [6 ,7 ]
Cheung, Mary N. B. [8 ,9 ]
Chow, Louis W. C. [1 ]
Li, Jin-le [6 ,7 ]
Tian, Ye [6 ,7 ]
Qing, Liu [1 ]
机构
[1] UNIMED Med Inst, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Li Ka Shing Fac Med, Sch Chinese Med, Pokfulam, Hong Kong, Peoples R China
[3] Sichuan Acad Med Sci, Dept Stomatol, Chengdu, Sichuan Provinc, Peoples R China
[4] Sichuan Prov Peoples Hosp, Chengdu, Sichuan Provinc, Peoples R China
[5] Guangzhou Med Univ, Stomatol Hosp, Guangzhou, Guangdong, Peoples R China
[6] Sichuan Univ, W China Hosp Stomatol, Dept Prosthodont, Chengdu, Sichuan, Peoples R China
[7] Sichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
[8] Jin Hua Dent, Chengdu 610041, Sichuan, Peoples R China
[9] Keenlink Dent Clin, Hong Kong, Hong Kong, Peoples R China
关键词
SINGLE-NUCLEOTIDE POLYMORPHISM; SOLUBLE CD14; HUMAN BETA-DEFENSIN-1; PERIODONTAL-DISEASE; EXPRESSION; ASSOCIATION; PROMOTER; RECEPTOR; DEFB1; ANTIBIOTICS;
D O I
10.1186/1479-5876-10-S1-S9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Periodontitis is a common disease that affects the periodontal tissue supporting the teeth. This disease is attributed to multiple risk factors, including diabetes, cigarette smoking, alcohol, pathogenic microorganisms, genetics and others. Human beta-defensin-1 (hBD-1) is a cationic antimicrobial peptide with cysteine-rich beta-sheets and broad-spectrum antimicrobial activity. CD14 is a protein involved in the detection of bacterial lipopolysaccharide (LPS) and has also been associated with periodontitis. This study investigates the single nucleotide polymorphic (SNP) region, -1654(V38I), of the human beta-defensin-1 (hBD-1) gene as well as the -159 region of the CD14 gene in subjects with chronic periodontitis. Methods: Blood samples from periodontally healthy subjects and periodontitis patients were obtained. DNA was extracted from the blood and was used to perform restriction digest at the polymorphic G1654A site of DEFB1 with the enzyme HincII. The polymorphic site 159TT of CD14 was digested with the enzyme AvaII. Enzyme-linked immunosorbent assay (ELISA) was performed on soluble samples to determine the protein expressions. Results: The control and patient groups expressed 35% and 38% 1654 A/A genotype of DEFB1, respectively. The A allele frequency of the control group was 40%, while the patient blood group was 54%. The mean hBD-1 protein levels of the control and patient samples were 102.83 pg/mL and 252.09 pg/mL, respectively. The genotype distribution of CD14 in healthy subjects was 16% for C/C, 26% for T/T and 58% for C/T. The genotype frequencies of CD14 in periodontitis patients were 10% for C/C, 43% for T/T and 47% for C/T. The CD14 protein expression determined by ELISA showed a mean protein level of the control samples at 76.28ng/mL and the patient blood samples at 179.27ng/mL with a p value of 0.001. Our study demonstrated that patients suffering from chronic periodontitis present more commonly with the 1654A/A genotype on the DEFB1 gene and the 159T/T genotype on the CD14 gene. Conclusions: This study purely investigated the association between periodontitis and one polymorphic site on both DEFB1 and CD14 gene, with the purpose of expanding knowledge for the future development in diagnostic markers or therapeutic interventions to combat this disease.
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页数:10
相关论文
共 59 条
[1]   Serum antibody levels in smoker and non-smoker Saudi subjects with chronic periodontitis [J].
Al-Ghamdi, Hamdan S. ;
Anil, Sukumaran .
JOURNAL OF PERIODONTOLOGY, 2007, 78 (06) :1043-1050
[2]  
[Anonymous], 2009, SAMPLE SIZE TABLES C
[3]  
[Anonymous], 1990, Adequacy of sample size in health studies, DOI DOI 10.2307/2532527
[4]  
Armitage G C, 1999, Ann Periodontol, V4, P1, DOI 10.1902/annals.1999.4.1.1
[5]   HBD-1 - A NOVEL BETA-DEFENSIN FROM HUMAN PLASMA [J].
BENSCH, KW ;
RAIDA, M ;
MAGERT, HJ ;
SCHULZKNAPPE, P ;
FORSSMANN, WG .
FEBS LETTERS, 1995, 368 (02) :331-335
[6]   Novel hairpin-shaped primer assay to study the association of the-44 single-nucleotide polymorphism of the DEFB1 gene with early-onset periodontal disease [J].
Boniotto, M ;
Hazbón, MH ;
Jordan, WJ ;
Lennon, GP ;
Eskdale, J ;
Alland, D ;
Gallagher, G .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2004, 11 (04) :766-769
[7]   The role of stress in periodontal disease and wound healing [J].
Boyapati, Lakshmi ;
Wang, Hom-Lay .
PERIODONTOLOGY 2000, 2007, 44 :195-210
[8]   Innate antimicrobial activity of nasal secretions [J].
Cole, AM ;
Dewan, P ;
Ganz, T .
INFECTION AND IMMUNITY, 1999, 67 (07) :3267-3275
[9]   Localized antimicrobial peptide expression in human gingiva [J].
Dale, BA ;
Kimball, JR ;
Krisanaprakornkit, S ;
Roberts, F ;
Robinovitch, M ;
O'Neal, R ;
Valore, EV ;
Ganz, T ;
Anderson, GM ;
Weinberg, A .
JOURNAL OF PERIODONTAL RESEARCH, 2001, 36 (05) :285-294
[10]   High expression levels of keratinocyte antimicrobial proteins in psoriasis compared with atopic dermatitis [J].
de Jongh, GJ ;
Zeeuwen, PLJM ;
Kucharekova, M ;
Pfundt, R ;
van der Valk, PG ;
Blokx, W ;
Dogan, A ;
Hiemstra, PS ;
van de Kerkhof, PC ;
Schalkwijk, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2005, 125 (06) :1163-1173