z-logo
open-access-imgOpen Access
K.Vita: a feasibility study of a blend of medium chain triglycerides to manage drug-resistant epilepsy
Author(s) -
Natasha E. Schoeler,
Michael Orford,
Umesh Vivekananda,
Zoe Simpson,
Baheerathi Van de Bor,
Hannah Smith,
Simona Balestrini,
Tricia Rutherford,
Erika Brennan,
James McKenna,
Bridget Lambert,
Tom Barker,
Richard Jackson,
Robin S. B. Williams,
Sanjay M. Sisodiya,
Simon Eaton,
Simon Heales,
J. Helen Cross,
Matthew C. Walker,
Sanjeev Rajakulendran,
Aikaterini Vezyroglou,
Suresh Pujar,
Judith Kalser,
Christin Eltze,
Sophia Varadkar,
Robert Robinson,
Shamima Rahman
Publication year - 2021
Publication title -
brain communications
Language(s) - English
Resource type - Journals
ISSN - 2632-1297
DOI - 10.1093/braincomms/fcab160
Subject(s) - discontinuation , tolerability , medicine , ketogenic diet , pediatrics , epilepsy , incidence (geometry) , adverse effect , psychiatry , physics , optics
This prospective open-label feasibility study aimed to evaluate acceptability, tolerability and compliance with dietary intervention with K.Vita, a medical food containing a unique ratio of decanoic acid to octanoic acid, in individuals with drug-resistant epilepsy. Adults and children aged 3–18 years with drug-resistant epilepsy took K.Vita daily whilst limiting high-refined sugar food and beverages. K.Vita was introduced incrementally with the aim of achieving ≤35% energy requirements for children or 240 ml for adults. Primary outcome measures were assessed by study completion, participant diary, acceptability questionnaire and K.Vita intake. Reduction in seizures or paroxysmal events was a secondary outcome. 23/35 (66%) children and 18/26 (69%) adults completed the study; completion rates were higher when K.Vita was introduced more gradually. Gastrointestinal disturbances were the primary reason for discontinuation, but symptoms were similar to those reported from ketogenic diets and incidence decreased over time. At least three-quarters of participants/caregivers reported favourably on sensory attributes of K.Vita, such as taste, texture and appearance, and ease of use. Adults achieved a median intake of 240 ml K.Vita, and children 120 ml (19% daily energy). Three children and one adult had ß-hydroxybutyrate >1 mmol/l. There was 50% (95% CI 39–61%) reduction in mean frequency of seizures/events. Reduction in seizures or paroxysmal events correlated significantly with blood concentrations of medium chain fatty acids (C10 and C8) but not ß-hydroxybutyrate. K.Vita was well accepted and tolerated. Side effects were mild and resolved with dietetic support. Individuals who completed the study complied with K.Vita and additional dietary modifications. Dietary intervention had a beneficial effect on frequency of seizures or paroxysmal events, despite absent or very low levels of ketosis. We suggest that K.Vita may be valuable to those with drug-resistant epilepsy, particularly those who cannot tolerate or do not have access to ketogenic diets, and may allow for more liberal dietary intake compared to ketogenic diets, with mechanisms of action perhaps unrelated to ketosis. Further studies of effectiveness of K.Vita are warranted.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom