Balakrishnan Ramakrishna

Balakrishnan Ramakrishna

orcid

Research Focus & Metrics

Academic Career Length

45Years (1982-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 November 2013 in Journal of Gastroenterology and Hepatology
Verified
Journal Article
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BRBalakrishnan Ramakrishna
Balakrishnan Ramakrishna

1 July 2012 in Journal of Clinical Gastroenterology
Verified
Journal Article
Closed access
FGFrancisco Guarner
Francisco Guarner
AKAamir G. Khan
Aamir G. Khan
JGJames Garisch
James Garisch
RERami Eliakim
Rami Eliakim
AGAlfred Gangl
Alfred Gangl
NKNayoung Kim
Nayoung Kim

31 July 2008 in Journal of Gastroenterology and Hepatology
Verified
Journal Article
Closed access
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Balamurugan RamadassBalamurugan Ramadass
Balamurugan Ramadass
EREthendhar Rajendiran
Ethendhar Rajendiran
SGSarah George
Sarah George
GSG Vijay Samuel
G Vijay Samuel
BRBalakrishnan Ramakrishna
Balakrishnan Ramakrishna

1 November 2014 in Clinical Infectious Diseases
Verified
Journal Article
Open access
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GKGerald T. Keusch
Gerald T. Keusch
DDDonna M. Denno
Donna M. Denno
RBRobert E. Black
Robert E. Black
CDChristopher Duggan
Christopher Duggan
RGRichard L. Guerrant
Richard L. Guerrant
TBThomas Brewer
Thomas Brewer
Stunting is common in young children in developing countries, and is associated with increased morbidity, developmental delays, and mortality. Its complex pathogenesis likely involves poor intrauterine and postnatal nutrition, exposure to microbes, and the metabolic consequences of repeated infections. Acquired enteropathy affecting both gut structure and function likely plays a significant role in this outcome, especially in the first few months of life, and serve as a precursor to later interactions of infection and malnutrition. However, the lack of validated clinical diagnostic criteria has limited the ability to study its role, identify causative factors, and determine cost-effective interventions. This review addresses these issues through a historical approach, and provides recommendations to define and validate a working clinical diagnosis and to guide critical research in this area to effectively proceed. Prevention of early gut functional changes and inflammation may preclude or mitigate the later adverse vicious cycle of malnutrition and infection.

1 January 2013 in Journal of Clinical Gastroenterology
Verified
Journal Article
Closed access
MFMichael Farthing
Michael Farthing
MSMohammed A. Salam
Mohammed A. Salam
GLGreger Lindberg
Greger Lindberg
PDPetr Dite
Petr Dite
IKIgor Khalif
Igor Khalif
ALAnton LeMair
Anton LeMair

3 February 2000 in New England Journal of Medicine
Verified
Journal Article
Open access
PDF file
BRBalakrishnan Ramakrishna
Balakrishnan Ramakrishna
SVS. Venkataraman
S. Venkataraman
PSP. Srinivasan
P. Srinivasan
PDPratap Dash
Pratap Dash
GYGraeme P. Young
Graeme P. Young
HBHenry J. Binder
Henry J. Binder
Although standard glucose-based oral rehydration therapy corrects the dehydration caused by cholera, it does not reduce the diarrhea. Short-chain fatty acids, which are produced in the colon from nonabsorbed carbohydrates, enhance sodium absorption. We conducted a study to determine the effects of an orally administered, nonabsorbed starch (i.e., one resistant to digestion by amylase) on fecal fluid loss and the duration of diarrhea in patients with cholera. We randomly assigned 48 adolescents and adults with cholera to treatment with standard oral rehydration therapy (16 patients), standard therapy and 50 g of rice flour per liter of oral rehydration solution (16 patients), or standard therapy and 50 g of high-amylose maize starch, an amylase-resistant starch, per liter of oral rehydration solution (16 patients). The primary end points were fecal weight (for every 12-hour period during the first 48 hours after enrollment) and the length of time to the first formed stool. The mean (±SD) fecal weights in the periods 12 to 24 hours, 24 to 36 hours, and 36 to 48 hours after enrollment were significantly lower in the resistant-starch group (2206±1158 g, 1810±1018 g, and 985±668 g) than in the standard-therapy group (3251± 766 g, 2621±1149 g, and 2498±1080 g; P=0.01, P= 0.04, and P=0.001, respectively). From 36 to 48 hours after enrollment, fecal weight was also significantly lower with the resistant-starch therapy than with the rice-flour therapy (985±668 g vs. 1790±866 g, P=0.01). The mean duration of diarrhea was significantly shorter with the resistant-starch therapy (56.7±18.6 hours) than with standard therapy alone (90.9±29.8 hours, P=0.001) or the rice-flour therapy (70.8±20.2 hours, P=0.05). Fecal excretion of starch was higher with the resistant-starch therapy (32.6±30.4) than with the standard therapy (11.7±4.1 g, P=0.002) or the rice-flour therapy (15.1±8.4 g, P=0.01). The addition of a resistant starch to oral rehydration solution reduces fecal fluid loss and shortens the duration of diarrhea in adolescents and adults with cholera.