Asymptomatic Bacteriuria Clinical Trial
Official title:
Effectiveness of Cranberry Ingestion on Bacterial Adhesion: Adjunct to Pilot Study of Daily Cranberry Ingestion of Cranberry Juice for the Prevention of Asymptomatic Bacteriuria in Pregnancy
This study is to help determine if drinking cranberry juice can decrease risk for asymptomatic bacteriuria (ASB). ASB occurs when there are bacteria in the urine without any symptoms. It will also see if there is a difference in this effect between pregnant and non-pregnant women.This research project is also designed to see what happens to bacterial binding to the lining of the bladder after drinking cranberry juice when special problems occur with pregnancy such as diabetes (a sugar metabolism problem) or ASB is already occurring.
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.
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