Kassir A
70, avenue du Point-du-Jour, 69005 Lyon, France.
Encephale. 2017 Feb;43(1):85-89. doi: 10.1016/j.encep.2016.08.002. Epub 2016 Sep 16.
Iron plays an essential role in balancing the various metabolism in the body. It is also involved in the synthesis of several neurotransmitters. Nutritional iron deficiency is one of the most widespread worldwide; it poses a great health challenge due to the consequences it entails.
The aim of this research study is to explore the percentage of psychiatric patients who have a deficiency in iron. In addition, the study investigates the efficacy of iron administered by oral treatment on psychiatric symptomatology among iron deficient patients. The research study utilized the martial biological results, which involved the observation of the level of iron deficiency among the outpatients of a local psychiatrist and assessor from the period of January 2012 until December 2013.
Out of 412 patients, 295 were women and 117 men. The age of the participants ranged from 16 to 89years, with an average age of 45years. The only exclusion criterion was a patient's refusal or inability to take the prescribed iron assessment test. We considered a transferrin saturation coefficient (TSC)<30% and/or a serum ferritin level≤50ng/mL to be "indicative" of obvious iron deficiency, and a ferritin level between 51 and 100ng/mL to be "suggestive" of iron deficiency. A plasma ferritin assay was performed at least once on all of the participants prior to any proposed iron treatment. A calculation of the TSC in 138 patients was requested due to suspected iron deficiency despite a blood ferritin level of>100ng/ml. A single method was utilized in the various laboratories to analyse the blood samples to determine whether there was a deficiency in iron. Only those patients with blood ferritin levels ≤100ng/mL and/or a TSC of<30% (335 patients) were subsequently given exclusively an oral iron treatment prescribed on its own or as a supplement or simultaneously with psychotropic treatment. The daily administered dose of elemental iron varied between 50 and 200mg a day.
About half of the women - 145 (35.19% of the subjects) - and 15 men (3.64% of the subjects) certainly had a deficiency in iron (blood ferritin level≤50ng/mL). Ninety women and 24 men (27.6% of the subjects) had blood ferritin levels between 51 and 100ng/mL indicating iron deficiency, and 28 women and 33 men (14.8% of the subjects) had a TSC of<30% despite a blood ferritin level of>100ng/mL. Overall, 335 patients (81.3% of the subjects) showed an iron deficiency based on the criteria we set. In the remaining 77 patients (18.7% of the subjects), all of them had blood ferritin levels>100ng/mL and some had TSC≤30%, while the remaining patients' TSC was unknown because it was not measured. The results indicated that there is an iron deficiency in 198 out of 240 patients suffering mostly from mood and behavioural disorders, in 101 out of 126 patients suffering mostly from anxiety disorders, in 18 out of 27 patients suffering mostly from sleep disorders, in 14 out of 15 patients suffering mostly from delusions of persecution, and in the 4 patients suffering mostly from burn out. There was evidence of regression/remission of psychiatric symptoms in 193 responsive patients whereas the remaining 142 patients were considered non-responsive. In the responsive patient category, 37 participants were treated with just iron, 52 received iron supplemented to the initial psychotropic treatment which was not fully effective, and 104 patients were treated with iron and prescribed psychotropic drugs simultaneously. The iron treatment seems to bring about a reduction - particularly through its mono-aminergic neurotransmitter synthesis-promoting action - in hyperemotivity, anxiety, irritability, aggressiveness, sadness, anhedonia, apathy, asthenia, sleep disorders, dysautonomia symptoms, eating disorders, restless-leg syndrome, cognitive performance and the likelihood of resorting to psychiatric admission. A daily elemental iron dose intake between 50 and 200mg/day by deficient patients appears to likely enhance the effects of the psychotropic drugs and even to act as an actual antidepressant. Many patients who received a prescription for iron and antidepressants showed few side effects related to antidepressants and a small number required psychiatric hospitalization. Patients considered unresponsive to iron therapy were those who left the study, were not assessed because the study's timeframe ended, still had an iron deficiency because they did not continuously take the medication, or suffered from somatic diseases which explains their resistance to treat the low iron level (nutritional imbalance, digestive or urinary or gynecological or iatrogenic diseases, sleep apnea).
Our clinical observation of two years in a local psychiatrist's clinic revealed that over 80% of patients had iron deficiency. Although the low iron level cannot explain all physical and psychiatric symptoms in patients, it is useful to note that more than half of the iron deficient patients responded favorably after an oral treatment of iron. This result leads to further investigation of the level of iron in psychiatric patients and to reconsider the iron range placed by the laboratories. In addition, it is crucial not to eliminate the possibility of iron deficiency in psychiatric patients. Further research studies are needed to set more specific and detailed criteria to determine the range of iron deficiency in order to support the findings of this study and optimize the care given to patients suffering from various disorders and psychiatric syndromes.
铁在平衡人体各种新陈代谢中起着至关重要的作用。它还参与多种神经递质的合成。营养性缺铁是全球最普遍的问题之一;因其带来的后果,它对健康构成了巨大挑战。
本研究旨在探究缺铁的精神科患者的比例。此外,该研究还调查了口服铁剂治疗对缺铁患者精神症状的疗效。该研究利用了临床生物学结果,包括观察2012年1月至2013年12月期间当地一位精神科医生和评估者门诊患者的缺铁水平。
在412名患者中,295名是女性,117名是男性。参与者的年龄在16至89岁之间,平均年龄为45岁。唯一的排除标准是患者拒绝或无法接受规定的铁评估测试。我们认为转铁蛋白饱和系数(TSC)<30%和/或血清铁蛋白水平≤50ng/mL为明显缺铁的“指征”,铁蛋白水平在51至100ng/mL之间为缺铁的“提示”。在对所有参与者进行任何提议的铁治疗之前,至少进行一次血浆铁蛋白测定。由于尽管血铁蛋白水平>100ng/ml但怀疑缺铁,对138名患者进行了TSC计算。各个实验室采用单一方法分析血样以确定是否缺铁。只有那些血铁蛋白水平≤100ng/mL和/或TSC<30%的患者(335名患者)随后仅接受单独开具的口服铁剂治疗,或作为补充剂,或与精神药物同时服用。每日给予的元素铁剂量在50至200mg/天之间。
约一半的女性——145名(占受试者的35.19%)——和15名男性(占受试者的3.64%)肯定缺铁(血铁蛋白水平≤50ng/mL)。90名女性和24名男性(占受试者的27.6%)血铁蛋白水平在51至100ng/mL之间表明缺铁,28名女性和33名男性(占受试者的14.8%)尽管血铁蛋白水平>100ng/mL但TSC<30%。总体而言,根据我们设定的标准,335名患者(占受试者的81.3%)显示缺铁。在其余77名患者(占受试者的18.7%)中,他们的血铁蛋白水平均>100ng/mL,一些患者TSC≤30%,而其余患者的TSC未知,因为未进行测量。结果表明,在240名主要患有情绪和行为障碍的患者中有198名缺铁,在126名主要患有焦虑症的患者中有101名缺铁,在27名主要患有睡眠障碍的患者中有18名缺铁,在15名主要患有被害妄想的患者中有14名缺铁,在4名主要患有倦怠的患者中也有缺铁。193名有反应的患者有精神症状缓解/减轻的证据,而其余142名患者被认为无反应。在有反应的患者类别中,37名参与者仅接受铁剂治疗,52名接受了补充铁剂的初始精神药物治疗,该治疗不完全有效,104名患者同时接受铁剂和开具的精神药物治疗。铁剂治疗似乎能减轻——特别是通过其促进单胺能神经递质合成的作用——过度情绪化、焦虑、易怒、攻击性、悲伤、快感缺失、冷漠、乏力、睡眠障碍、自主神经功能紊乱症状、饮食失调、不安腿综合征、认知能力以及寻求精神科住院治疗的可能性。缺铁患者每日摄入50至200mg/天的元素铁剂量似乎可能增强精神药物的效果,甚至起到实际的抗抑郁作用。许多接受铁剂和抗抑郁药处方的患者与抗抑郁药相关的副作用较少,少数患者需要精神科住院治疗。被认为对铁剂治疗无反应的患者是那些退出研究的患者、因研究时间框架结束未进行评估的患者、因未持续服药仍缺铁的患者,或患有躯体疾病从而解释了他们对治疗低铁水平有抵抗性的患者(营养失衡、消化或泌尿或妇科或医源性疾病、睡眠呼吸暂停)。
我们在当地精神科诊所进行的两年临床观察表明,超过80%的患者缺铁。尽管低铁水平不能解释患者所有的身体和精神症状,但值得注意的是,超过一半的缺铁患者在口服铁剂治疗后反应良好。这一结果促使进一步研究精神科患者的铁水平,并重新考虑实验室设定的铁范围。此外,至关重要的是不要排除精神科患者缺铁的可能性。需要进一步的研究来设定更具体和详细的标准,以确定缺铁范围,以支持本研究的结果,并优化对患有各种疾病和精神综合征患者的护理。