Effectiveness of Cranberry Ingestion on Bacterial Adhesion: An Adjunct Study
Schlüsselwörter
Abstrakt
Beschreibung
This study is an adjunct to a proposal the premise of which is daily cranberry ingestion during pregnancy may be an effective preventative approach to development of asymptomatic bacteriuria (ASB), a condition which predisposes to both preterm birth and upper urinary tract infection. We proposed to NCCAM a pilot randomized, controlled trial (RCT) in which pregnant women beyond 12 weeks' gestational age will be assigned to one of three schedules for cranberry ingestion: Group A will consume cranberry juice twice a day with breakfast and dinner; Group B will consume cranberry juice at breakfast followed by placebo at dinner; and Group C will consume placebo with meals. Both the cranberry juice and placebo will be of scientific grade, provided by an NIH-contractor. Both are well-characterized, presenting a low-carbohydrate load and low-calorie content per dose (40 cal per 8 oz. dose). Our intent is to 1) generate data comparing the frequency of asymptomatic bacteriuria in pregnant women consuming cranberry juice daily versus placebo, and to 2) create the infrastructure to complete this pilot study and to gather sufficient data to support an R01 for a larger, multi-center RCT focused on the prevention of ASB in pregnancy with daily cranberry juice ingestion.
The reviewers of our proposal enumerated specific weaknesses including 1) a need to evaluate urine from cranberry treated patients, and 2) consideration of bacterial virulence/adherence. The additional variable of gestational diabetes also received comment from the reviewers, and we acknowledge that predisposition in the Hispanic population to this obstetrical complication could impact results. A constituent of cranberries is fructose, which has been implicated in the inhibition of E. coli with type 1 fimbriae (mannose-sensitive) (2). We hypothesize that the glucosuria associated with diabetes in pregnancy may influence the effectiveness of cranberry to prevent asymptomatic bacteriuria.
We must address these weaknesses to strengthen chances for continued funding and competitive renewal.
We have made inquiries with other researchers, and have discovered no direct urine or serum assays by which to measure cranberry metabolites. We understand that there is an R21 proposal under consideration to develop a urinary assay for this purpose under the same RFA. Amy Howell, PhD, of the Marucci Center for Blueberry/Cranberry Research of Rutgers University, one of the field's foremost researchers in this field, and others have indirectly assayed compliance to cranberry by evaluating adherence of piliated E. coli strains before and after cranberry exposure (1). In response to the recent call for proposals for faculty research from the UCI Committee on Research, I proposed this pilot study in collaboration with Dr. Howell.
In this proposal, we will collect the urine from various participants in the R21 trial so as to characterize the effect of cranberry juice ingestion on bacterial adherence. We will ask women to collect their urine for a four-hour time period including first-morning void. The urine samples will be sent to Dr. Howell's laboratory at Rutgers University for analysis. We will collect urine from pregnant women who are assigned to cranberry and to placebo, and from those women who develop bacteriuria following cranberry and following placebo ingestion. We also plan to identify a group of reproductive age, healthy, and non-pregnant women to ingest the active cranberry product or placebo for three days, and on the third day, collect a four-hour timed sample in the same manner as the pregnant women in our control group.
Termine
Zuletzt überprüft: | 10/31/2017 |
Zuerst eingereicht: | 07/23/2007 |
Geschätzte Einschreibung eingereicht: | 07/23/2007 |
Zuerst veröffentlicht: | 07/24/2007 |
Letztes eingereichtes Update: | 11/16/2017 |
Letztes Update veröffentlicht: | 12/17/2017 |
Datum der ersten eingereichten Ergebnisse: | 12/02/2009 |
Datum der ersten eingereichten QC-Ergebnisse: | 05/12/2010 |
Datum der ersten veröffentlichten Ergebnisse: | 06/07/2010 |
Tatsächliches Startdatum der Studie: | 07/31/2006 |
Geschätztes primäres Abschlussdatum: | 01/31/2008 |
Voraussichtliches Abschlussdatum der Studie: | 01/31/2008 |
Zustand oder Krankheit
Intervention / Behandlung
Dietary Supplement: Cranberry Juice
Dietary Supplement: Placebo 2xday
Phase
Armgruppen
Arm | Intervention / Behandlung |
---|---|
Active Comparator: Cranberry 2xday Cranberry juice (C) two times daily, a.m. and p.m. | |
Active Comparator: Cranberry + Placebo De-Activated Cranberry juice in the am, then placebo (P) in the pm | |
Placebo Comparator: Placebo 2xday Placebo in the form of juice two times daily in the a.m. and p.m. | Dietary Supplement: Placebo 2xday De-Activated Cranberry juice in the am, then placebo (P) in the pm |
Zulassungskriterien
Altersberechtigt für das Studium | 18 Years Zu 18 Years |
Studienberechtigte Geschlechter | Female |
Akzeptiert gesunde Freiwillige | Ja |
Kriterien | Inclusion Criteria: - Intrauterine pregnancy - Documented fetal viability (either by fetal heart tones present by Doppler auscultation, or by ultrasonic visualization of cardiac motion - Estimated gestational age by last menstrual period and/or by ultrasonographic fetal measurements of 16 weeks or less Exclusion Criteria: - Exclusion criteria will include: - Suspected non-viable or ectopic gestation - Patient desires pregnancy termination - Significant underlying medical complication, such as chronic hypertension, insulin-requiring diabetes, chronic renal failure, cardiac disease, sickle cell disease, etc. - Maternal age less than 18 years - Patient is currently on or has received within the two weeks prior to enrollment antimicrobial therapy for reasons other than urinary tract infection. |
Ergebnis
Primäre Ergebnismaße
1. Antimicrobial Activity of Urine From Pregnant Subjects Following Cranberry Juice Cocktail (CJC) [7 months, from enrollment at 3 months of pregnancy to delivery]