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- Publisher Website: 10.1902/jop.2008.080033
- Scopus: eid_2-s2.0-55749101608
- PMID: 18980513
- WOS: WOS:000260933900009
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Article: Nifedipine intake increases the risk for periodontal destruction in subjects with type 2 diabetes mellitus
Title | Nifedipine intake increases the risk for periodontal destruction in subjects with type 2 diabetes mellitus | ||||
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Authors | |||||
Keywords | Diabetes Epidemiology Periodontitis Risk factors | ||||
Issue Date | 2008 | ||||
Publisher | American Academy of Periodontology. The Journal's web site is located at http://www.perio.org | ||||
Citation | Journal Of Periodontology, 2008, v. 79 n. 11, p. 2054-2059 How to Cite? | ||||
Abstract | Background: This study investigated the possible association of nifedipine (NIF) intake and diabetes mellitus (DM) with periodontal destruction. Methods: A group of Chinese subjects (N = 1,083, age: 63 ± 8.7 years) were screened. Three hundred fifty-eight non-smokers with hypertension were selected for the study and were grouped based on DM status as non-DM and DM groups, DM(-) and DM(+) respectively. NIF(+) and NIF(-) indicated NIF intake or not. The groups were further divided: NIF(-)/DM(-) (n = 135); NIF(+)/DM(-) (n = 108); NIF(-)/DM(+) (n = 64); and NIF(+)/DM(+) (n = 51). The periodontal conditions in anterior teeth were assessed using plaque index, sulcus bleeding index, clinical attachment loss (AL), probing depth (PD), and the number of missing teeth. Results: Using analysis of covariance, NIF intake was associated with mean PD and extent of PD ≥4 mm in the non-DM and DM groups. The subjects in the NIF(+)/DM(+) subgroup showed greater mean AL and percentage of sites with AL ≥5 mm and AL ≥7 mm than those in NIF(-)/DM(+) subgroup, whereas no significant difference existed between subjects in NIF(-)/DM(-) and NIF(+)/DM(-) subgroups. The NIF(+)/DM(+) subgroup exhibited a greater percentage of sites with AL ≥5 mm (35.5%) compared to the other three subgroups (24.7% for NIF[-]/DM[-], P = 0.004; 25.0% for NIF[+]/DM[-], P = 0.007; and 25.2% for NIF[-]/DM[+], P = 0.016). Logistic regression analysis showed that the NIF(+)/DM(+) subgroup had a significantly higher risk for having 7gt;10% of sites with AL ≥5 mm compared to the NIF(-)/DM(-) subgroup (odds ratio [OR] = 2.9; 95% confidence interval [CI]: 1.2 to 7.4; P = 0.022), the NIF(+)/DM(-) subgroup (OR = 3.1; 95% CI: 1.2 to 8.1; P = 0.020), and the NIF(-)/DM(+) subgroup (OR = 5.1; CI: 1.8 to 14.3; P = 0.002). Conclusion: NIF intake may increase the risk for periodontal destruction in patients with type 2 DM. | ||||
Persistent Identifier | http://hdl.handle.net/10722/58115 | ||||
ISSN | 2023 Impact Factor: 4.2 2023 SCImago Journal Rankings: 1.362 | ||||
ISI Accession Number ID |
Funding Information: This study was supported by Capital Medical Development Fund (2003 to 2005) from the Beijing Municipal Health Bureau, Beijing, China. The authors report no conflicts of interest related to this study. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, X | en_HK |
dc.contributor.author | Luan, Q | en_HK |
dc.contributor.author | Wang, X | en_HK |
dc.contributor.author | Sha, Y | en_HK |
dc.contributor.author | He, L | en_HK |
dc.contributor.author | Cao, C | en_HK |
dc.contributor.author | Jin, L | en_HK |
dc.date.accessioned | 2010-05-31T03:24:03Z | - |
dc.date.available | 2010-05-31T03:24:03Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Journal Of Periodontology, 2008, v. 79 n. 11, p. 2054-2059 | en_HK |
dc.identifier.issn | 0022-3492 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/58115 | - |
dc.description.abstract | Background: This study investigated the possible association of nifedipine (NIF) intake and diabetes mellitus (DM) with periodontal destruction. Methods: A group of Chinese subjects (N = 1,083, age: 63 ± 8.7 years) were screened. Three hundred fifty-eight non-smokers with hypertension were selected for the study and were grouped based on DM status as non-DM and DM groups, DM(-) and DM(+) respectively. NIF(+) and NIF(-) indicated NIF intake or not. The groups were further divided: NIF(-)/DM(-) (n = 135); NIF(+)/DM(-) (n = 108); NIF(-)/DM(+) (n = 64); and NIF(+)/DM(+) (n = 51). The periodontal conditions in anterior teeth were assessed using plaque index, sulcus bleeding index, clinical attachment loss (AL), probing depth (PD), and the number of missing teeth. Results: Using analysis of covariance, NIF intake was associated with mean PD and extent of PD ≥4 mm in the non-DM and DM groups. The subjects in the NIF(+)/DM(+) subgroup showed greater mean AL and percentage of sites with AL ≥5 mm and AL ≥7 mm than those in NIF(-)/DM(+) subgroup, whereas no significant difference existed between subjects in NIF(-)/DM(-) and NIF(+)/DM(-) subgroups. The NIF(+)/DM(+) subgroup exhibited a greater percentage of sites with AL ≥5 mm (35.5%) compared to the other three subgroups (24.7% for NIF[-]/DM[-], P = 0.004; 25.0% for NIF[+]/DM[-], P = 0.007; and 25.2% for NIF[-]/DM[+], P = 0.016). Logistic regression analysis showed that the NIF(+)/DM(+) subgroup had a significantly higher risk for having 7gt;10% of sites with AL ≥5 mm compared to the NIF(-)/DM(-) subgroup (odds ratio [OR] = 2.9; 95% confidence interval [CI]: 1.2 to 7.4; P = 0.022), the NIF(+)/DM(-) subgroup (OR = 3.1; 95% CI: 1.2 to 8.1; P = 0.020), and the NIF(-)/DM(+) subgroup (OR = 5.1; CI: 1.8 to 14.3; P = 0.002). Conclusion: NIF intake may increase the risk for periodontal destruction in patients with type 2 DM. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Academy of Periodontology. The Journal's web site is located at http://www.perio.org | en_HK |
dc.relation.ispartof | Journal of Periodontology | en_HK |
dc.subject | Diabetes | - |
dc.subject | Epidemiology | - |
dc.subject | Periodontitis | - |
dc.subject | Risk factors | - |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Aged, 80 and over | en_HK |
dc.subject.mesh | Analysis of Variance | en_HK |
dc.subject.mesh | Calcium Channel Blockers - adverse effects - therapeutic use | en_HK |
dc.subject.mesh | Cohort Studies | en_HK |
dc.subject.mesh | Cross-Sectional Studies | en_HK |
dc.subject.mesh | Diabetes Mellitus, Type 2 - complications | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Hypertension - complications - drug therapy | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Nifedipine - adverse effects - therapeutic use | en_HK |
dc.subject.mesh | Periodontal Diseases - chemically induced - complications | en_HK |
dc.subject.mesh | Periodontal Index | en_HK |
dc.subject.mesh | Risk Factors | en_HK |
dc.subject.mesh | Severity of Illness Index | en_HK |
dc.subject.mesh | Single-Blind Method | en_HK |
dc.title | Nifedipine intake increases the risk for periodontal destruction in subjects with type 2 diabetes mellitus | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-3492&volume=79&spage=2054&epage=2059&date=2008&atitle=Nifedipine+intake+increases+the+risk+for+periodontal+destruction+in+subjects+with+type+2+diabetes+mellitus | en_HK |
dc.identifier.email | Jin, L:ljjin@hkucc.hku.hk | en_HK |
dc.identifier.authority | Jin, L=rp00028 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1902/jop.2008.080033 | en_HK |
dc.identifier.pmid | 18980513 | - |
dc.identifier.scopus | eid_2-s2.0-55749101608 | en_HK |
dc.identifier.hkuros | 154123 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-55749101608&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 79 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 2054 | en_HK |
dc.identifier.epage | 2059 | en_HK |
dc.identifier.isi | WOS:000260933900009 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Li, X=36014295300 | en_HK |
dc.identifier.scopusauthorid | Luan, Q=14625404700 | en_HK |
dc.identifier.scopusauthorid | Wang, X=8885333800 | en_HK |
dc.identifier.scopusauthorid | Sha, Y=7102249983 | en_HK |
dc.identifier.scopusauthorid | He, L=7403374572 | en_HK |
dc.identifier.scopusauthorid | Cao, C=7401501946 | en_HK |
dc.identifier.scopusauthorid | Jin, L=7403328850 | en_HK |
dc.identifier.issnl | 0022-3492 | - |