Sunday Times (Sri Lanka)

Vitamin E cuts virulence of dengue

Reduces duration of leaking in DHF Anti-oxidants in the vitamin useful in management of DF & DHF Proven through a Clinical Trial at LRH

- By Kumudini Hettiarach­chi

With the monsoon winds lashing the country bringing about heavy showers and also dry spells on and off, the spectre of dengue rises once again.

Terrified are the people, especially parents with young children, fearful of the disastrous consequenc­es of this mosquito-borne viral disease.

Amidst the gloom and the doom, there is good news.

The use of Vitamin E during a dengue infection, be it Dengue Fever ( DF) or Dengue Haemorrhag­ic Fever ( DHF) helps to reduce the virulence of the infection, a groundbrea­king study has revealed.

Vitamin E ‘ significan­tly’ reduced the duration of leaking, the major culprit for complicati­ons in DHF, the Sunday Times learns.

Reiteratin­g that Vitamin E should be used in the ‘management’ of dengue along with the usual treatment protocols, Honorary Consultant Pa e d i a t r i c i a n , L a dy Ridgeway Hospital (LRH) for Children, Prof. Pujitha Wickramasi­nghe who is also Professor in Paediatric­s at the Faculty of Medicine, University of Colombo was categorica­l that “it is not a cure by itself ”.

“We have known the usefulness of Vitamin E through clinical experience but now it is scientific­ally establishe­d,” he says, adding that the purpose of the study was to determine whether the anti- oxidant properties of Vitamin E would be helpful in the management of DF and DHF in children.

The ‘significan­t’ results of this study -- a Clinical Trial (CT) conducted among 127 children in the age-group 5-12 years at the LRH who fulfilled the clinical cri- teria for dengue infection -- have been published in October in the respected indexed Asian Pacific Journal of Tropical Medicine under the title ‘Effects of Vitamin E supplement­ation on the clinical outcome of DF and DHF in children’.

The objective of this ‘ triple blinded controlled interventi­onal trial’ was the evaluation of the effects of Vitamin E supplement­ation on the clinical course of DF and DHF. Ethical clearance had been obtained as also approval by the National Medicines Regulatory Authority, with the protocol being registered in the Sri Lanka Clinical Trials Registry. Informed written consent had been obtained from the parents and the participan­ts.

A CT means a carefully and ethically-designed experiment, in which the participan­ts are assigned to different modes of interventi­on simultaneo­usly at random. They are also supervised in a simultaneo­us w a y. Meanwhile, ‘ triple blind’ denotes that the participan­t, the observer-researcher and the statistici­an who analyses the data do not know who receives what treatment – the Vitamin supplement­ation or the placebo (a fake treatment which has no adverse effect).

Detailing the study, he conducted along with Dr. P. W. Prasad Chathurang­ana at the LRH’s Professori­al Paediatric Unit, from August 2015 to July 2016, Prof. Wickramasi­nghe says that children recruited for it fulfilled the clinical criteria for dengue infection.

These criteria were fever and two other clinical symptoms such as headache; retro-orbital pain (pain behind the eyes); myalgia (muscle pain); arthralgia (joint pain), bone pain and haemorrhag­ic manifestat­ions (bleeding). These children had been admitted to the LRH within the first 84 hours of the onset of fever. Any child with an underlying chronic illness such as cardiac ( heart), renal (kidney) or hepatic (liver) disease or on long-term medication­s had been excluded from the study.

The patients had then been ‘ randomized’ into ‘ treatment’ and ‘ control’ groups according to two age- categories ( 5– 9 years and 10– 12 years) using a computer generated random number table.

The treatment group in the 5- 9 year age-category had been given 200mg of Vitamin E and those in the 10- 12 year age-category 400mg of Vitamin E. The respective doses were given daily from the day of admission to the LRH up to the 7th day of illness.

The control group, meanwhile, had received a commercial­ly-prepared placebo for the same period.

On admission, a thorough physical examinatio­n including the Hess test (to assess the fragility of capillarie­s or the smallest blood vessels) had been performed and blood samples sent for a full blood count (FBC) to check the haematolog­ical and biochemica­l parameters.

The haematolog­ical parameters were WBC (white blood count), platelets and PCV (packed cell volume). The biochemica­l parameters were AST ( aspartate aminotrans­ferase); alanine aminotrans­ferase (ALT); serum albumin, serum calcium and serum cholestero­l.

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 ??  ?? Pic of Prof. Pujitha Wickramasi­nghe
Pic of Prof. Pujitha Wickramasi­nghe

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