維生素缺乏會導致精神分裂症嗎? Could some people with schizophrenia in poorer nations simply have a vitamin deficiency?

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Could some people with schizophrenia in poorer nations simply have a vitamin deficiency?

A new hypothesis may hold the key to solving four medical mysteries associated with the chronic brain disorder

UNIVERSITY OF TORONTO

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IMAGE: COULD SOME PEOPLE WITH SCHIZOPHRENIA IN POORER NATIONS SIMPLY HAVE A VITAMIN DEFICIENCY? view more 

 

CREDIT: UNIVERSITY OF TORONTO

Four unsolved mysteries around schizophrenia have long plagued the medical community, but a new hypothesis identifying a common link between them and an almost forgotten epidemic of a disease called pellagra could have profound implications for our understanding of psychosis in poorer nations. The new hypothesis has implications for how a subgroup of people with active psychosis could be potentially screened, treated, and cured.

The idea behind the hypothesis occurred to Esme Fuller-Thomson, professor at the University of Toronto’s Factor-Inwentash Faculty of Social Work (FIFSW) after learning about recent research conducted in South India. This study newly identified a link between schizophrenia and a variant of the gene NAPRT1, which lowers the body’s ability to use niacin, or Vitamin B3, which naturally occurs in meat, poultry, fish, and eggs.

“When I read this study a light bulb went on in my head,” says Fuller-Thomson, who published the hypothesis in the journal Schizophrenia Research this month with doctoral student, Rukshan Mehta. “This seems to be the missing link that explains all these medical mysteries.”

The researchers speculate that there is a critical interaction between an expectant mother’s prenatal niacin deficiency due to malnourishment and the NAPRT1 variant that impedes the fetus’ ability to use niacin. This interaction between the gene and the prenatal environment may predispose the offspring to develop a psychotic disorder.

Several studies indicate that the offspring of mothers who experience famine in their first trimester of pregnancy have double the chance of developing schizophrenia. Most researchers assume nutrient deficiency must be playing a role, but the particular nutrient has yet to be identified. Fuller Thomson now speculates that niacin may be the key nutrient involved.

The identification of the NAPRT1 risk variant also provides some insights into a second medical mystery: Normally when people are given high doses of niacin, their skin reddens and can tingle, burn, or itch; however, many individuals with schizophrenia experience limited or no flushing to the same high dose amount. The presence of a gene inhibiting the uptake of niacin may explain why people with schizophrenia do not show the same reddening of the skin in response to large doses: they simply have a lower ability to absorb the vitamin.

Pellagra could be an important part of the puzzle as well. Between 1906 to 1940, almost 3 million Americans developed pellagra due to a niacin deficient diet. The symptoms include dermatitis, dementia, and death. In four to ten percent of cases, active psychosis develops, which mimics schizophrenia. Pellagra became the leading cause of death in psychiatric hospitals in the Southern United States in that era.

“Treatment with niacin quickly and permanently cures the disease including the psychosis and the dermatitis,” reported co-author Rukshan Mehta, an MSW graduate of the FIFSW who is currently a doctoral candidate in Nutrition & Health Sciences at Emory University. “By 1941, flour was fortified with niacin in the USA and the disease was soon after largely eradicated.”

Today, diagnosis of pellagra is rare, but Fuller-Thomson and Mehta wonder if it might be going undetected in the developing world.

In most cases of pellagra, a bad rash is the first symptom, and this is usually how the disorder is diagnosed. The researchers hypothesize that individuals with psychosis and the risky gene variant may not present with dermatitis. This would result in the patients being misclassified as having schizophrenia instead of the easily treatable psychosis associated with niacin deficiency.

Fuller-Thomson and Mehta’s hypothesis also provides new insights into the most perplexing of the medical mysteries associated with schizophrenia: studies by the World Health Organization show that patients with schizophrenia in the developing world recover at a markedly higher rate than those in western nations, despite the fact that those in the west receive more extensive medical interventions.?If some of the schizophrenia patients in the developing world were, in fact, undiagnosed pellagra cases, their psychosis may have been cured inadvertently by simply spending time in a hospital where nutritious niacin-rich food such as meat and eggs are provided.

The final medical mystery has been generating debate for half a century. Six randomized controlled trials conducted in Saskatchewan, Canada in the 1950s found excellent results treating patients with schizophrenia with high doses of niacin, but multiple efforts to replicate the study in the 1970s found the intervention ineffective.

The 1950s Canadian studies were conducted among patients born in the Great Depression before niacin fortification of flour was adopted. “It is highly probable that those with schizophrenia in Saskatchewan had malnourished, niacin-deficient mothers,” says Fuller-Thomson. “If the patients’ psychosis was due to undiagnosed pellagra, of course the niacin treatment would be effective. The pregnant mothers of the participants in the later study benefited from universal niacin fortification and therefore the patients were unlikely to have pellagra.”

The researchers emphasize that both a correct diagnosis and medical supervision of niacin treatment for pellagra are essential. “Taking high dose niacin can cause life-threatening problems if not properly monitored,” cautions Fuller-Thomson.

“We acknowledge that this hypothesis is highly speculative, but feel further exploration of these ideas are warranted,” says Fuller-Thomson.?”In cases where the psychosis is due to pellagra, these patients could be inexpensively, quickly, and permanently cured with high dose niacin, allowing them to live a healthy normal life.”

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For more please information, please contact:

Esme Fuller-Thomson, Professor & Director, Institute of Life Course & Aging
Factor-Inwentash Faculty of Social Work &Department of Family & Community Medicine,?University of Toronto
Cell: 416-209-3231
Email: [email protected]

Publication Details: Fuller-Thomson, E., Mehta, R. (2019). Could a gene-environment interaction between NAPRT1 risk allele and pre-natal niacin deficiency explain 4 medical mysteries of schizophrenia research? Schizophrenia Research (Published online ahead of print)

A copy of the paper is available to credentialed journalists upon request.

Please contact: [email protected] or call 416-209-3231.

維生素缺乏會導致精神分裂症嗎?

5000/5000Character limit: 5000圍繞精神分裂症的四個未解之謎長期困擾著醫學界,但是一個新的假說可以確定它們之間的共同聯繫以及幾乎被人們遺忘的一種名為“糙皮病”的流行病,這可能對我們對貧困國家的精神病的理解產生深遠的影響。新的假設對如何篩查,治療和治愈患有活動性精神病的亞組人群具有影響。

這項假設的想法是多倫多大學因特文塔什社會工作學院(FIFSW)教授埃斯梅·富勒·湯姆森(Esme Fuller-Thomson)在了解了最近在印度南部進行的研究後提出的。這項研究新發現了精神分裂症與NAPRT1基因變體之間的聯繫,該基因降低了人體使用菸酸或維生素B3的能力,而菸酸或維生素B3自然存在於肉,禽,魚和蛋中。

富勒-湯姆森(Fuller-Thomson)說:“當我讀到這項研究時,腦袋裡一直閃著一個燈泡。”他與博士生Rukshan Mehta一起在本月的精神分裂症研究雜誌上發表了這一假設。 “這似乎是解釋所有這些醫學奧秘的缺失環節。”

研究人員推測,由於營養不良,準媽媽的產前菸酸缺乏症與NAPRT1變異之間存在著關鍵的相互作用,該變異會阻礙胎兒使用菸酸的能力。基因與產前環境之間的這種相互作用可能使後代容易患上精神病。

多項研究表明,在懷孕的頭三個月經歷飢荒的母親的後代有兩倍的機會患上精神分裂症。大多數研究人員認為營養缺乏症必鬚髮揮作用,但是具體的營養物質尚未確定。富勒湯姆森(Fuller Thomson)現在推測,菸酸可能是其中所涉及的關鍵營養素。

對NAPRT1風險變異的識別還為第二個醫學謎團提供了一些見解:通常,當人們服用高劑量的菸酸時,他們的皮膚發紅,並可能刺痛,灼熱或發癢。但是,許多精神分裂症患者在相同的高劑量下會出現潮紅的次數有限或沒有潮紅。抑製菸酸攝取的基因的存在可以解釋為什麼精神分裂症患者在大劑量反應下不會表現出相同的皮膚變紅:他們只是吸收維生素的能力較低。

佩拉格拉可能也是難題的重要組成部分。在1906年至1940年之間,由於菸酸缺乏飲食,近300萬美國人患了糙皮病。症狀包括皮炎,癡呆和死亡。在百分之四到百分之十的情況下,會發展為模仿精神分裂症的積極精神病。那個時代,佩拉格拉(Pellagra)成為美國南部精神病醫院的主要死亡原因。

合著者Rukshan Mehta報告說:“菸酸治療可永久性地治愈包括精神病和皮炎在內的疾病。” FIFSW的MSW畢業生Rukshan Mehta報告說,他目前是Emory大學營養與健康科學的博士候選人。 “到1941年,在美國麵粉中都添加了菸酸,而這種病在很大程度上被消滅了。”

如今,對糙皮病的診斷很少見,但富勒-湯姆森和梅塔(Mehta)懷疑在發展中國家是否會發現這種病。

在大多數的糙皮病中,皮疹是第一個症狀,這通常是診斷該疾病的方法。研究人員假設患有精神病和高風險基因變異的個體可能不會出現皮炎。這將導致患者被誤認為患有精神分裂症,而不是與菸酸缺乏有關的易於治療的精神病。

Fuller-Thomson和Mehta的假設也為與精神分裂症有關的最令人困惑的醫學奧秘提供了新的見解:世界衛生組織的研究表明,儘管有精神分裂症,但發展中國家的康復率明顯高於西方國家西方人接受更廣泛的醫學乾預的事實。如果發展中國家的某些精神分裂症患者實際上是未經診斷的糙皮病,那麼他們的精神病可能只是由於在有營養菸酸的醫院裡度過的時間而被無意治愈。提供了豐富的食物,例如肉和蛋。

最終的醫學奧秘已經引起了半個世紀的爭論。 1950年代在加拿大薩斯喀徹溫省進行的六項隨機對照試驗發現,使用高劑量菸酸治療精神分裂症患者的療效優異,但在1970年代重複進行的多次研究發現干預無效。

1173/5000Character limit: 50001950年代加拿大的研究是在採用菸酸強化麵粉之前在大蕭條時期出生的患者中進行的。富勒-湯姆森說:“薩斯喀徹溫省患有精神分裂症的母親極有營養不良,菸酸缺乏的母親,”。 “如果患者的精神病是由於未診斷出的糙皮病,菸酸治療當然是有效的。後來研究的參與者的懷孕母親從普遍的菸酸強化中受益,因此患者不太可能患上糙皮病。”

研究人員強調,菸葉病菸酸治療的正確診斷和醫學監督至關重要。富勒湯姆森警告說:“如果不適當監控,服用大劑量菸酸可能會危及生命。”

富勒-湯姆森說:“我們承認這一假設具有高度的推測性,但認為有必要進一步探討這些想法。”如果精神病是由糙皮病引起的,可以廉價,快速,永久治愈這些患者。高劑量的菸酸,使他們過上健康的正常生活。”

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