Examination of the Distribution of Nitrate Reducing Bacteria in the Human Oral Cavity

Non-smoking Clinical Trial

— REBOC  

Official title:

Examination of the Distribution of Nitrate Reducing Bacteria in the Human Oral Cavity

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03068962
• Other study ID #: 32/16
• Status: Not yet recruiting
• Phase: N/A
• First received: February 22, 2017
• Last updated: February 27, 2017
• Start date: March 2017
• Est. completion date: March 2018

Study information

• Verified date: February 2017
• Source: University of Reading
• Contact: Julie A Lovegrove, BSc, PhD
• Phone: 0044118378
• Email: j.a.lovegrove[@]reading.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Dietary nitrate have been shown to have health benefits including lowering blood pressure (Hobbs et al, 2012), improving endothelial function and inhibiting platelet aggregation in healthy humans (Lidder & Webb, 2013). The main sources of dietary nitrate in the human diet are vegetables such as beetroot. Nitrates are converted to nitrites then nitric oxide (NO), following their reduction by commensal oral bacteria and those residing in the gastrointestinal tract (Hord, Tang, & Bryan, 2009; Lidder & Webb, 2013). A recent study has shown following elimination of oral bacteria by the use of a chlorhexidine based antiseptic mouthwash, the conversion of nitrate to nitrite is prevented and this is accompanied by a statistically significant increase in blood pressure in normotensive subjects (Kapil et al., 2013). To date, very few studies have investigated the potential role of these oral bacteria in control of blood pressure and if there are any inter and intra-individual differences in bacterial composition.

Description:

Volunteers will be provided with an outline of the study and asked to complete a medical and lifestyle questionnaire (in person, email or over the phone). Potentially suitable participants will be identified and asked to attend a screening session during which the study will be explained in more detail before a consent form is signed. Anthropometric measurements will then be taken such as weight, height and blood pressure. Subjects who meet the inclusion criteria will be invited to a further screening session during which time a dentist will check for dental diseases (e.g. current dental cavities or periodontal infection). The oral bacteria samples will be collected in the morning on site at the Department of Food and Nutritional Sciences (Hugh Sinclair Unit of Human Nutrition) on four visit days (including screening visit).On the day before each study visit the volunteers will need to have a low nitrate diet, refrain from strenuous exercise and alcohol, and drink low nitrate mineral water. They will be required to fast overnight and only drink water. In the morning, they will be asked to refrain from brushing their teeth or using mouthwash.

When they arrive in the unit in the fasted state, they will then be randomised to one of three treatments:

• Rinse mouth with low nitrate Buxton mineral water followed by holding 10 ml of beetroot juice (~6 mmol nitrate) for 5 min,

• Rinse mouth with low nitrate Buxton mineral water followed by holding 10 ml of low nitrate mineral water in the mouth for 5 min or

• Rinse with antiseptic mouthwash before holding 10 ml of beetroot juice in the mouth for 5 min.

After 5 mins of holding low nitrate water or beetroot juice in the mouth, they will then spit the whole mouth rinse into a sterile ice-chilled tube.

To evaluate the nitrate reduction in different areas of the oral cavity, the researchers will put filter paper squares which have been soaked in water or beetroot juice in different areas of their mouth (rear, mid and front tongue, tooth surface, buccal surface, hard palate, and sublingual). Volunteers will be required to keep the filter papers in their mouth for 90 seconds before they are removed.

Finally, the oral bacteria will be collected from the 7 sites by sliding a piece of sterile oral floss between the 2 back molars and by swabbing a micro brush along the buccal cervical margin of premolars and rear, mid, front tongue. Saliva will be obtained using a sterile cotton swab. All samples will be placed into sterile tubes (Eppendorfs). Mouth rinse will be collected in sterile ice-chilled Falcon tubes.

Volunteers will then be provided with a light breakfast before they leave the unit. Facilities will be available for participants to brush their teeth before they leave the clinical unit.

The study visits will be separated by at least 1 week.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: March 2018
• Est. primary completion date: September 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Male and female

• A signed consent form

• Age 18-55 years

• Non-smoking, healthy individuals

• BMI 18.5 - 30 kg/m2

Exclusion Criteria:

• Diagnosed with a chronic illness

• Individuals with food allergies or allergies to medicated mouthwash or ingredients in the oral products

• Requirements to take long-term medication active on the oral cavity or taken antibiotics within the last 3 months

• Current diagnosis of dental caries, gingivitis, or periodontal disease or chronic oral complaints or Existing oral pathology (active caries lesions and/or periodontal disease; mucosal lesions; poor occlusion)

• Current smoker (regular and electronic cigarettes and cigars)

• Participating in a dietary intervention study.

• Excessive alcohol consumption (> 21 units/wk male, >14 units/wk female)

• Females who are pregnant or lactating

• Reduced salivary flow (unstimulated flow less than 0.1 ml/min);

• less than four natural (enamel) buccal surfaces of upper molars available;

• presence of fixed or removable oral appliances (e.g., dentures, orthodontic wires)

Related Conditions & MeSH terms

• No Dental Disease
• Non-smoking
• Stomatognathic Diseases

Intervention

Other:
• beetroot Juice
Beetroot Juice
• Buxton water
natural mineral water
• antiseptic mouthwash then beetroot juice
Chlorhexidine glocunate

Locations

Country	Name	City	State
United Kingdom	Department of Food and Nutritional Sciences, University of Reading	Reading	Berkshire

Sponsors (1)

Lead Sponsor	Collaborator
University of Reading

Country where clinical trial is conducted

United Kingdom, 

References & Publications (4)

Hobbs DA, Kaffa N, George TW, Methven L, Lovegrove JA. Blood pressure-lowering effects of beetroot juice and novel beetroot-enriched bread products in normotensive male subjects. Br J Nutr. 2012 Dec 14;108(11):2066-74. doi: 10.1017/S0007114512000190. — View Citation

Hord NG, Tang Y, Bryan NS. Food sources of nitrates and nitrites: the physiologic context for potential health benefits. Am J Clin Nutr. 2009 Jul;90(1):1-10. doi: 10.3945/ajcn.2008.27131. Review. — View Citation

Kapil V, Haydar SM, Pearl V, Lundberg JO, Weitzberg E, Ahluwalia A. Physiological role for nitrate-reducing oral bacteria in blood pressure control. Free Radic Biol Med. 2013 Feb;55:93-100. doi: 10.1016/j.freeradbiomed.2012.11.013. — View Citation

Lidder S, Webb AJ. Vascular effects of dietary nitrate (as found in green leafy vegetables and beetroot) via the nitrate-nitrite-nitric oxide pathway. Br J Clin Pharmacol. 2013 Mar;75(3):677-96. doi: 10.1111/j.1365-2125.2012.04420.x. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	oral bacteria sample will be collected to Identification of nitrate reductase-positive bacteria in the oral cavity and capacity to reduce dietary nitrate	In vitro method will be used to isolate the nitrate reducing bacteria then 16SrDNA sequencing will be used to identify the species of these bacteria.	1 year
Secondary	Identify the major sites in the human oral cavity which contain nitrate reducing bacteria.	filter paper will be put in different sites around the oral cavity in human trial and then removed before analysis using chemiluminescence to determine nitrate and nitrite concentrations.	1 year