Impact of high dose omega-3 polyunsaturated fatty acid treatment on measures of microvascular function and vibration perception in non-alcoholic fatty liver disease: results from the randomised WELCOME trial

Aims/hypothesis The effect of n-3 fatty acid treatment on vibration perception thresholds (VPTs) and cutaneous microvascular reactivity is not known. We tested whether: (1) a 15-18 month treatment with high dose (4 g/day) docosahexaenoic (DHA) plus eicosapentaenoic (EPA) acid improved VPT and micro...

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Main Authors: McGormick, Keith G. (Author), Scorletti, Eleonora (Author), Bhatia, Lokpal (Author), Calder, Philip C. (Author), Griffin, Michael .J (Author), Clough, Geraldine F. (Author), Byrne, Christopher D. (Author)
Format: Article
Language:English
Published: 2015-08.
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LEADER 03562 am a22002173u 4500
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042 |a dc 
100 1 0 |a McGormick, Keith G.  |e author 
700 1 0 |a Scorletti, Eleonora  |e author 
700 1 0 |a Bhatia, Lokpal  |e author 
700 1 0 |a Calder, Philip C.  |e author 
700 1 0 |a Griffin, Michael .J.  |e author 
700 1 0 |a Clough, Geraldine F.  |e author 
700 1 0 |a Byrne, Christopher D.  |e author 
245 0 0 |a Impact of high dose omega-3 polyunsaturated fatty acid treatment on measures of microvascular function and vibration perception in non-alcoholic fatty liver disease: results from the randomised WELCOME trial 
260 |c 2015-08. 
856 |z Get fulltext  |u https://eprints.soton.ac.uk/376679/1/__soton.ac.uk_ude_PersonalFiles_Users_lce_mydocuments_Eprints%2520-%2520Prof%2520Byrne_Accepted%2520pubs%2520for%2520Eprints_Diabetologia%2520Journal%2520Accepted%2520April%25202015.pdf 
856 |z Get fulltext  |u https://eprints.soton.ac.uk/376679/2/art%25253A10.1007%25252Fs00125-015-3628-2.pdf 
520 |a Aims/hypothesis The effect of n-3 fatty acid treatment on vibration perception thresholds (VPTs) and cutaneous microvascular reactivity is not known. We tested whether: (1) a 15-18 month treatment with high dose (4 g/day) docosahexaenoic (DHA) plus eicosapentaenoic (EPA) acid improved VPT and microvascular reactivity in patients with non-alcoholic fatty liver disease; and (2) there are associations between VPT, microvascular reactivity and metabolic variables. Methods In the completed single centre, randomised, parallel group, placebo controlled Wessex Evaluation of fatty Liver and Cardiovascular markers in non-alcoholic fatty liver disease with OMacor thErapy (WELCOME) trial, we tested the effect of DHA+EPA on VPT at 125 Hz (big toe) and the cutaneous hyperaemic response (forearm) to arterial occlusion (ratio of maximum to resting blood flux [MF/RF]). Allocation and dispensing was carried out by an independent research pharmacist; all participants and research team members were blinded to group assignment. Results In all, 51 and 49 patients were randomised to placebo and DHA+EPA, respectively (mean age 51.4 years). Of these, 32 had type 2 diabetes. Forty-six (placebo) and 47 (DHA+EPA) patients completed the study; there were no important adverse (or unexpected) effects or side effects. In multivariable-adjusted regression models (intention-to-treat analyses), DHA+EPA treatment was associated with an increase in VPT (? coefficient 1.49 [95% CI 0.04, 2.94], p?=?0.04). For VPT, the adjusted mean differences (95% CIs) in the placebo and DHA+EPA treatment groups were ?0.725 (?1.71, 0.25) and 0.767 (?0.21, 1.75) m/s2, respectively. With DHA+EPA treatment, there was no change in MF/RF (? coefficient 0.07 [95% CI ?0.56, 0.70], p?=?0.84), the adjusted mean differences (95% CIs) in the placebo and DHA+EPA treatment groups were ?0.549 (?1.03, ?0.07) and ?0.295 (?0.77, 0.18) respectively. VPT was independently associated with age (? coefficient 0.019 [95% CI 0.010, 0.029], p?<?0.0001) and MF/RF (? coefficient ?0.074 [95% CI ?0.132, ?0.016], p?=?0.013), but not with diabetes (p?=?0.38). Conclusions/interpretation High dose n-3 fatty acid treatment did not improve measures of microvascular function or vibration perception. Ageing and microvascular reactivity are associated with a measure of peripheral nerve function. Trial registration: ClinicalTrials.gov NCT00760513 Funding: The study was funded by the National Institute for Health Research UK and Diabetes UK. 
540 |a accepted_manuscript 
655 7 |a Article