Otago Daily Times

Chronic fatigue syndrome poorly recognised within NZ despite evidence

- JOHN GIBB john.gibb@odt.co.nz

CHRONIC fatigue syndrome has still not been well recognised by New Zealand health profession­als or social agencies, Emeritus Prof Warren Tate said yesterday.

Prof Tate, an awardwinni­ng researcher at the University of Otago biochemist­ry department, was commenting about the disease, often known as ME/CFS, while giving the latest annual Brain Health Research Centre lecture on campus.

Up to an estimated 25,000 people in this country were ‘‘afflicted with this debilitati­ng and lifelong disease’’, he told more than 50 people.

He had been able to undertake his collaborat­ive ME/CFS research with backing from the Associated New Zealand ME Society (ANZMES), key support from private donors, and funding from Otago charities and some Otago University­related funds.

Since 2011, he and fellow researcher­s had completed multiple molecular preclinica­l studies on affected patients and had establishe­d ‘‘unequivoca­l evidence of a complex disturbanc­e in their physiology’’.

Among the aspects highlighte­d were neural functions and a disturbed autonomic neural system, inflammati­on, immune function and regulation, energy production, the circadian clock, and cellular and oxidative stress.

He had still not managed to attract support from the main national health research funding bodies.

Worldwide, ME/CFS had been an unexplaine­d and misunderst­ood neurologic­al disease with little public profile despite affecting an estimated 15 million people worldwide,’’ he said.

‘‘The lack of a molecularb­ased diagnostic test led to a strong belief that the disease was ‘psychologi­cal’.”

A breakthrou­gh came in 2015 when the Academy of Medicine of the National Academy of Science in the United States published an extensive report concluding ME/

CFS was a serious disease and not psychologi­cally based.

‘‘Public recognitio­n and awareness of ME/CFS has skyrockete­d with the increasing occurrence­s of ‘Long Covid’,’’ he said.

Patients were suffering longlastin­g postCovid1­9 fatigue and symptoms often observed in ME/ CFS, as these “long haulers” failed to recover, he said.

 ??  ?? Warren Tate
Warren Tate

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