Sahar Mohammed
Queen Mary University of London
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Publication
Featured researches published by Sahar Mohammed.
Neurogastroenterology and Motility | 2010
Natalia Zarate; Adam D. Farmer; Rodney Grahame; Sahar Mohammed; Charles H. Knowles; S. M. Scott; Qasim Aziz
Background Unexplained gastrointestinal (GI) symptoms and joint hypermobility (JHM) are common in the general population, the latter described as benign joint hypermobility syndrome (BJHS) when associated with musculo‐skeletal symptoms. Despite overlapping clinical features, the prevalence of JHM or BJHS in patients with functional gastrointestinal disorders has not been examined.
Neurogastroenterology and Motility | 2010
Phillip Dinning; N. Zarate; Linda M. Hunt; Sergio E. Fuentealba; Sahar Mohammed; Michal M. Szczesniak; D. Z. Lubowski; Sean L. Preston; P. D. Fairclough; Peter J. Lunniss; S. M. Scott; Ian J. Cook
Background The morphology, motor responses and spatiotemporal organization among colonic propagating sequences (PS) have never been defined throughout the entire colon of patients with slow transit constipation (STC). Utilizing the technique of spatiotemporal mapping, we aimed to demonstrate ‘manometric signatures’ that may serve as biomarkers of the disorder.
American Journal of Physiology-gastrointestinal and Liver Physiology | 2010
Natalia Zarate; Sahar Mohammed; Emma O'Shaughnessy; Margaret Newell; Etsuro Yazaki; Norman S. Williams; Peter J. Lunniss; Jack R. Semler; S. Mark Scott
Stereotypical changes in pH occur along the gastrointestinal (GI) tract. Classically, there is an abrupt increase in pH on exit from the stomach, followed later by a sharp fall in pH, attributed to passage through the ileocecal region. However, the precise location of this latter pH change has never been conclusively substantiated. We aimed to determine the site of fall in pH using a dual-scintigraphic technique. On day 1, 13 healthy subjects underwent nasal intubation with a 3-m-long catheter, which was allowed to progress to the distal ileum. On day 2, subjects ingested a pH-sensitive wireless motility capsule labeled with 4 MBq (51)Chromium [EDTA]. The course of this, as it travelled through the GI tract, was assessed with a single-headed γ-camera using static and dynamic scans. Capsule progression was plotted relative to a background of 4 MBq ¹¹¹Indium [diethylenetriamine penta-acetic acid] administered through the catheter. Intraluminal pH, as recorded by the capsule, was monitored continuously, and position of the capsule relative to pH was established. A sharp fall in pH was recorded in all subjects; position of the capsule relative to this was accurately determined anatomically in 9/13 subjects. In these nine subjects, a pH drop of 1.5 ± 0.2 U, from 7.6 ± 0.05 to 6.1 ± 0.1 occurred a median of 7.5 min (1-16) after passage through the ileocecal valve; location was either in the cecum (n = 5), ascending colon (n = 2), or coincident with a move from the cecum to ascending colon (n = 2). This study provides conclusive evidence that the fall in pH seen within the ileocolonic region actually occurs in the proximal colon. This phenomenon can be used as a biomarker of transition between the small and large bowel and validates assessment of regional GI motility using capsule technology that incorporates pH measurement.
Neurogastroenterology and Motility | 2010
Sahar Mohammed; Peter J. Lunniss; Natalia Zarate; Adam D. Farmer; Rodney Grahame; Qasim Aziz; S. M. Scott
Background Previous studies report an association between joint hypermobility (JHM), as a clinical feature of underlying connective tissue (CT) disorder, and pelvic organ prolapse. However, its association with rectal evacuatory dysfunction (RED) has not been evaluated. To investigate the prevalence of JHM in the general population and in patients with symptoms of RED referred for anorectal physiological investigation.
Alimentary Pharmacology & Therapeutics | 2015
Y. T. Wang; Sahar Mohammed; A. D. Farmer; Duolao Wang; N. Zarate; Anthony Hobson; Per M. Hellström; J. R. Semler; Braden Kuo; S. S. Rao; William L. Hasler; Michael Camilleri; S. M. Scott
The wireless motility capsule (WMC) offers the ability to investigate luminal gastrointestinal (GI) physiology in a minimally invasive manner.
Neurogastroenterology and Motility | 2010
Phillip Dinning; Natalia Zarate; Michal M. Szczesniak; Sahar Mohammed; Sean L. Preston; P. D. Fairclough; Peter J. Lunniss; Ian J. Cook; S. M. Scott
Background Colonic manometry is performed using either colonoscopically assisted catheter placement, after bowel preparation, or nasocolonic intubation of the unprepared bowel. There has been little systematic evaluation of the effects of bowel cleansing upon colonic propagating pressure wave sequences.
World Journal of Gastroenterology | 2014
Adam D. Farmer; Sahar Mohammed; George E. Dukes; S. Mark Scott; Anthony Hobson
AIM To ascertain whether caecal pH is different in patients with irritable bowel syndrome (IBS), whose primary symptoms are bloating and distension, to healthy controls. METHODS Motility and pH data were reviewed from 16 patients with Rome III defined IBS and 16 healthy controls, who had undergone a wireless motility capsule (WMC) study using a standardized protocol. Motility measures were anchored around known anatomical landmarks as identified by compartmental pH changes. Sixty-minute epochs were used to quantify antral, duodenal, ileal, caecal and distal colonic contractility. The maximum and minimum pH was measured either side of the ileo-caecal junction. RESULTS No differences were seen in motility parameters, compartmental transit times or maximal ileal pH between the two groups. Caecal pH was significantly lower in patients compared to controls (5.12 ± 0.05 vs 6.16 ± 0.15, P < 0.0001). The ileal:caecal Δchange was greater in patients than controls (-2.63 ± 0.08 vs -1.42 ± 0.11, P < 0.0001). There was a significant correlation between caecal pH and right colonic contractility (r = 0.54, P = 0.002). CONCLUSION Patients with bloating and distension have a lower caecal pH compared to controls. The measurement of caecal pH using the WMC provides a quantifiable biomarker of fermentation potentially identifying those patients that may preferentially benefit from antibiotic or dietary interventions.
Neurogastroenterology and Motility | 2013
Lukasz Wiklendt; Sahar Mohammed; S. M. Scott; Philip G. Dinning
Background Manual analysis of data acquired from manometric studies of colonic motility is laborious, subject to laboratory bias and not specific enough to differentiate all patients from control subjects. Utilizing a cross‐correlation technique, we have developed an automated analysis technique that can reliably differentiate the motor patterns of patients with slow transit constipation (STC) from those recorded in healthy controls.
Alimentary Pharmacology & Therapeutics | 2018
Adam D. Farmer; Anne-Marie Langmach Wegeberg; Birgitte Brock; Anthony R. Hobson; Sahar Mohammed; S. M. Scott; C. E. Bruckner-Holt; J. R. Semler; William L. Hasler; P. M. Hellström; Asbjørn Mohr Drewes; Christina Brock
The wireless motility capsule concurrently measures temperature, pH and pressure as it traverses the gastrointestinal tract.
The Journal of Physiology | 2018
Rubina Aktar; Madusha Peiris; Asma Fikree; Vincent Cibert-Goton; Maxim Walmsley; Iain R. Tough; Paulo da Silva Watanabe; Eduardo J. de Almeida Araujo; Sahar Mohammed; Jean-Marie Delalande; David C. Bulmer; S. Mark Scott; Helen M. Cox; Nicol C. Voermans; Qasim Aziz; L. Ashley Blackshaw
Tenascin‐X (TNX) is an extracellular matrix glycoprotein with anti‐adhesive properties in skin and joints. Here we report the novel finding that TNX is expressed in human and mouse gut tissue where it is exclusive to specific subpopulations of neurones. Our studies with TNX‐deficient mice show impaired defecation and neural control of distal colonic motility that can be rescued with a 5‐HT4 receptor agonist. However, colonic secretion is unchanged. They are also susceptible to internal rectal intussusception. Colonic afferent sensitivity is increased in TNX‐deficient mice. Correspondingly, there is increased density of and sensitivity of putative nociceptive fibres in TNX‐deficient mucosa. A group of TNX‐deficient patients report symptoms highly consistent with those in the mouse model. These findings suggest TNX plays entirely different roles in gut to non‐visceral tissues – firstly a role in enteric motor neurones and secondly a role influencing nociceptive sensory neurones Studying further the mechanisms by which TNX influences neuronal function will lead to new targets for future treatment.