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2.
Curr Opin Gastroenterol ; 36(2): 110-117, 2020 03.
Article in English | MEDLINE | ID: mdl-31895229

ABSTRACT

PURPOSE OF REVIEW: Trace elements are vital components involved in major body functions. Cases of trace elements deficiencies are increasingly encountered in clinical practice, although often underrecognized. This review gives a thorough insight into the newest findings on clinical situations associated with trace elements deficiencies in children and adults, their recognition and management. RECENT FINDINGS: Trace elements deficiencies are frequently found in various conditions, most commonly in burns, bariatric surgery, intestinal failure, renal replacement therapy, oncology, critical illness and cardiac surgery. The main trace elements involved are selenium, zinc, copper and iron. Trace elements deficiencies are associated with increased risk of morbidity and mortality. Recognition of clinical signs of trace elements deficiencies can be challenging. Although trace elements supplementation is indisputable in many circumstances, it is still debatable in other situations such as sepsis and cardiac surgery. SUMMARY: Recent findings on trace elements deficiencies could have important implications on health outcomes. Trace elements delivery is a core component of nutritional care. Front-line clinicians should be aware of at-risk clinical situations to provide correct and timely intervention. Future research should be directed towards investigating the potential benefits of antioxidant trace elements supplementation in children in whom studies are scarce, especially in critical conditions such as burns, sepsis and cardiac surgery.


Subject(s)
Deficiency Diseases/etiology , Trace Elements/deficiency , Deficiency Diseases/diagnosis , Deficiency Diseases/therapy , Humans , Trace Elements/administration & dosage
3.
Curr Gastroenterol Rep ; 22(1): 5, 2020 Jan 29.
Article in English | MEDLINE | ID: mdl-31997099

ABSTRACT

PURPOSE OF REVIEW: Inflammatory bowel disease (IBD) is often diagnosed during adolescence and can have a deep impact on the physical, hormonal, developmental, and psychosocial changes associated with this life period. The purpose of this review is to address the particular manifestations of IBD (such as growth and pubertal delay), health maintenance issues, and treatment considerations in the adolescent. RECENT FINDINGS: The need for a multidisciplinary approach to recognize and address growth and pubertal delay, bone health, as well as the psychosocial impact of IBD on the adolescent has been increasingly recognized as an integral part of IBD care in this population. Vaccinations schedule, preventive health measures, and promoting compliance with care are particularly important during adolescence. Replacing nutrients deficits is also crucial: in particular, vitamin D has been shown to play a role in the gut immune system, and adequate vitamin D levels might promote IBD remission. Iron replacement should be done by intravenous route since oral iron is poorly absorbed in chronic inflammatory states. Finally, recent data have shed light on the increased risk of particular types of lymphoma in adolescent on thiopurines, whereas biologic therapies, in particular, anti-TNF, now are positioned as a preferred and effective steroid-sparing agents in moderate to severe IBD. Management of adolescents with IBD is not without significant challenges. An early implementation of steroid-sparing therapies, a multidisciplinary treatment approach, and a dynamic physician-patient relationship are essential to achieve remission, prevent disease-related complications but also optimize developmental, physical, and psychosocial health, and encourage compliance and transition to adult care.


Subject(s)
Deficiency Diseases/therapy , Inflammatory Bowel Diseases/therapy , Adolescent , Adolescent Health , Deficiency Diseases/etiology , Humans , Inflammatory Bowel Diseases/complications
4.
Khirurgiia (Mosk) ; (10): 95-103, 2020.
Article in Russian | MEDLINE | ID: mdl-33047592

ABSTRACT

The article presents an algorithm for perioperative nutritional support of surgical patients operated on as planned. Today, planned surgical care is provided in accordance with the canons of the accelerated rehabilitation Program (ARP). The relevance of the problem of nutritional insufficiency, which is an important component of ARP, is due to the dependence of the results of surgical treatment on the initial nutritional status of the patient. Methods of screening for nutritional deficiency and options for correcting protein-energy disorders are described. The predominant method is the enteral delivery of nutrients and energy. Oral supplemental nutrition by sipping is a convenient way to correct nutritional disorders at all stages of the perioperative period.


Subject(s)
Elective Surgical Procedures , Malnutrition/therapy , Nutritional Support/methods , Perioperative Care/methods , Administration, Oral , Deficiency Diseases/diagnosis , Deficiency Diseases/therapy , Dietary Supplements , Enhanced Recovery After Surgery , Enteral Nutrition/methods , Humans , Malnutrition/diagnosis , Mass Screening , Nutritional Status , Perioperative Period
5.
Curr Opin Clin Nutr Metab Care ; 22(3): 223-229, 2019 05.
Article in English | MEDLINE | ID: mdl-30893089

ABSTRACT

PURPOSE OF REVIEW: Iron deficiency remains highly prevalent in women and young children in low-income and middle-income countries. To prevent the potentially life-long consequences of iron deficiency when occurring during early life, the WHO recommends iron supplementation of pregnant women and young children. However, increasing evidence of limited efficacy and risk of current iron intervention strategies are cause of concern. This review aims to highlight recent advances and challenges of established and novel intervention strategies for the prevention of iron deficiency during the first 1000 days in low-income and middle-income countries. RECENT FINDINGS: Recent meta-analyses and trials challenged the WHO's current recommendation to provide iron-folic acid rather than multiple micronutrient supplements during routine antenatal care. Furthermore, several studies explored optimal windows for iron supplementation, such as prior to conception. Studies are demonstrating that infectious and noninfectious inflammation is compromising the efficacy of iron interventions in vulnerable groups. Therefore, strategies addressing iron deficiency should focus on targeting infection and inflammation while simultaneously providing additional iron. Furthermore, both iron deficiency and iron supplementation may promote an unfavourable gut microbiota. Recent trials in infants indicate that the provision of a prebiotic together with iron may alleviate the adverse effects of iron on the gut microbiome and gut inflammation, and may even enhance iron absorption. SUMMARY: Recent studies highlight the need for and potential of novel intervention strategies that increase the efficacy and limit the potential harm of universal iron supplementation.


Subject(s)
Anemia, Iron-Deficiency , Deficiency Diseases , Iron , Anemia, Iron-Deficiency/prevention & control , Anemia, Iron-Deficiency/therapy , Child, Preschool , Deficiency Diseases/prevention & control , Deficiency Diseases/therapy , Developing Countries , Female , Humans , Infant , Infant, Newborn , Iron/blood , Iron/therapeutic use , Iron Deficiencies , Poverty , Pregnancy , Pregnancy Complications/prevention & control , Pregnancy Complications/therapy
6.
PLoS Comput Biol ; 14(11): e1006503, 2018 11.
Article in English | MEDLINE | ID: mdl-30388104

ABSTRACT

Multiscale modeling provides a very powerful means of studying complex biological systems. An important component of this strategy involves coarse-grained (CG) simplifications of regions of the system, which allow effective exploration of complex systems. Here we studied aspects of CG modeling of the human zinc transporter ZnT2. Zinc is an essential trace element with 10% of the proteins in the human proteome capable of zinc binding. Thus, zinc deficiency or impairment of zinc homeostasis disrupt key cellular functions. Mammalian zinc transport proceeds via two transporter families: ZnT and ZIP; however, little is known about the zinc permeation pathway through these transporters. As a step towards this end, we herein undertook comprehensive computational analyses employing multiscale techniques, focusing on the human zinc transporter ZnT2 and its bacterial homologue, YiiP. Energy calculations revealed a favorable pathway for zinc translocation via alternating access. We then identified key residues presumably involved in the passage of zinc ions through ZnT2 and YiiP, and functionally validated their role in zinc transport using site-directed mutagenesis of ZnT2 residues. Finally, we use a CG Monte Carlo simulation approach to sample the transition between the inward-facing and the outward-facing states. We present our structural models of the inward- and outward-facing conformations of ZnT2 as a blueprint prototype of the transporter conformations, including the putative permeation pathway and participating residues. The insights gained from this study may facilitate the delineation of the pathways of other zinc transporters, laying the foundations for the molecular basis underlying ion permeation. This may possibly facilitate the development of therapeutic interventions in pathological states associated with zinc deficiency and other disorders based on loss-of-function mutations in solute carriers.


Subject(s)
Cation Transport Proteins/metabolism , Models, Theoretical , Zinc/metabolism , Cation Transport Proteins/genetics , Computational Biology/methods , Deficiency Diseases/metabolism , Deficiency Diseases/therapy , Homeostasis , Humans , Monte Carlo Method , Mutagenesis, Site-Directed , Permeability , Zinc/deficiency
7.
J Pak Med Assoc ; 69(5): 722-724, 2019 May.
Article in English | MEDLINE | ID: mdl-31105296

ABSTRACT

A 12-year-old boy who underwent gastric wedge resection was transferred to our hospital because of vomiting, growth failure, and weight loss in January, 2016. We tried to restore his general condition by maintaining additional nutritional supply through peripheral parenteral nutrition (PN). However, continuous vomiting, weight loss, and superior mesenteric artery syndrome persisted because of low treatment compliance. The findings of hyponatraemia and bicytopenia did not improve. Bone marrow biopsy was performed, and it revealed copper deficiency. PN with additional micronutrient agents, including copper, were administered. In particular, invasive diagnosis and treatment, and adequate education improved the treatment compliance of the child. His copper deficiency and bicytopenia improved, and his weight and dietary intake also increased. We confirmed that treatment compliance is important in paediatric patients with malnutrition. In chronic malnutrition, attention should also be paid to deficiency of micronutrients such as copper, which can lead to haematologic problems.


Subject(s)
Anemia/etiology , Child Nutrition Disorders/complications , Copper/deficiency , Deficiency Diseases/complications , Leukopenia/etiology , Anorexia , Child , Child Nutrition Disorders/therapy , Chronic Disease , Deficiency Diseases/therapy , Dietary Supplements , Enteral Nutrition , Gastrectomy , Humans , Ileostomy , Male , Parenteral Nutrition , Patient Compliance , Superior Mesenteric Artery Syndrome , Vomiting , Weight Loss
8.
Indian J Med Res ; 148(5): 503-510, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30666977

ABSTRACT

Iodine deficiency disorders (IDDs) constitute a significant public health problem globally. In India, the entire population is prone to IDDs due to deficiency of iodine in the soil of the sub-continent and thus both animal and plant source food grown on the iodine-deficient soil. IDDs encompass the spectrum of disability and disease and include goitre, cretinism, hypothyroidism, abortion, stillbirth, brain damage, learning disabilities, mental retardation, psychomotor defects, hearing and speech impairment. Iodine deficiency is known to be the single largest cause of preventable brain damage. IDDs with their causal association with brain development, cognition, and learning disabilities impair the human resource development and progress of the country. The children born in iodine-deficient regions on an average have 13.5 intelligence quotient (IQ) points lesser than children born in iodine-sufficient regions. IDD control programme in India is a public health success story, with 92 per cent of the population consuming iodized salt. The partnership between government agencies, academic institutions, salt industry, development agencies and civil society has been key to achieve this success story. The sustainable elimination of iodine deficiency in India is within reach, what is required is accelerated and coordinated effort by all key stakeholder at national and State level.


Subject(s)
National Health Programs/organization & administration , Deficiency Diseases/epidemiology , Deficiency Diseases/etiology , Deficiency Diseases/therapy , Humans , India/epidemiology , Intersectoral Collaboration , Iodine/deficiency , Public Health/methods
9.
Indian J Med Res ; 148(5): 511-521, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30666978

ABSTRACT

Micronutrients play an important role in the proper growth and development of the human body and its deficiency affects the health contributing to low productivity and vicious cycle of malnutrition, underdevelopment as well as poverty. Micronutrient deficiency is a public health problem affecting more than one-fourth of the global population. Several programmes have been launched over the years in India to improve nutrition and health status of the population; however, a large portion of the population is still affected by micronutrient deficiency. Anaemia, the most common form of micronutrient deficiency affects almost 50 to 60 per cent preschool children and women, while vitamin A deficiency and iodine-deficiency disorders (IDD) have improved over the years. This review focuses on the current scenario of micronutrient (anaemia, vitamin A, iodine, vitamin B12, folate, ferritin, zinc, copper and vitamin C) status in the country covering national surveys as well as recent studies carried out.


Subject(s)
Deficiency Diseases , Micronutrients , National Health Programs/organization & administration , Deficiency Diseases/epidemiology , Deficiency Diseases/etiology , Deficiency Diseases/therapy , Humans , India/epidemiology , Micronutrients/classification , Micronutrients/deficiency , Nutritional Status , Public Health/methods
10.
Indian J Med Res ; 148(5): 522-530, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30666979

ABSTRACT

Nutrient requirements and recommended dietary allowances (RDAs) are set and revised periodically by the Indian Council of Medical Research. These are meant to guide the population and provide policy directions regarding nutrient requirements corresponding to a healthy population. This review article provides an overview of the current recommendations (RDA, 2010) and the challenges faced by the committee to contextualize RDA to the Indian scenario which has a background of double burden of malnutrition, diverse dietary habits but predominantly home-based cereal-pulse vegetarian diet with low bioavailability of several nutrients and lower consumption of packaged fortified foods. The need for country-specific requirements and harmonization of methodologies related to nutrient requirements and RDA are also discussed. The recommendations fixed for iron have been provided in detail as an example. The measures to carry forward RDA revisions to ensure its sustainability have been emphasized.


Subject(s)
Deficiency Diseases , Nutrients , Nutrition Policy , Nutritional Requirements , Deficiency Diseases/epidemiology , Deficiency Diseases/etiology , Deficiency Diseases/therapy , Feeding Behavior , Humans , India , Nutrients/classification , Nutrients/deficiency , Public Health/methods , Recommended Dietary Allowances
12.
Nutr Neurosci ; 19(5): 213-23, 2016 Jun.
Article in English | MEDLINE | ID: mdl-25909152

ABSTRACT

Hypophosphatemia (HP) with or without intracellular depletion of inorganic phosphate (Pi) and adenosine triphosphate has been associated with central and peripheral nervous system complications and can be observed in various diseases and conditions related to respiratory alkalosis, alcoholism (alcohol withdrawal), diabetic ketoacidosis, malnutrition, obesity, and parenteral and enteral nutrition. In addition, HP may explain serious muscular, neurological, and haematological disorders and may cause peripheral neuropathy with paresthesias and metabolic encephalopathy, resulting in confusion and seizures. The neuropathy may be improved quickly after proper phosphate replacement. Phosphate depletion has been corrected using potassium-phosphate infusion, a treatment that can restore consciousness. In severe ataxia and tetra paresis, complete recovery can occur after adequate replacement of phosphate. Patients with multiple risk factors, often with a chronic disease and severe HP that contribute to phosphate depletion, are at risk for neurologic alterations. To predict both risk and optimal phosphate replenishment requires assessing the nutritional status and risk for re-feeding hypophosphatemia. The strategy for correcting HP depends on the severity of the underlying disease and the goal for re-establishing a phosphate balance to limit the consequences of phosphate depletion.


Subject(s)
Deficiency Diseases/diet therapy , Dietary Supplements , Hypophosphatemia/diet therapy , Nervous System Diseases/physiopathology , Phosphates/therapeutic use , Animals , Deficiency Diseases/diagnosis , Deficiency Diseases/etiology , Deficiency Diseases/therapy , Dietary Supplements/adverse effects , Humans , Hypophosphatemia/diagnosis , Hypophosphatemia/physiopathology , Hypophosphatemia/therapy , Infusions, Intravenous , Nervous System Diseases/blood , Nervous System Diseases/etiology , Nutritional Status , Phosphates/administration & dosage , Phosphates/adverse effects , Phosphates/deficiency , Phosphorus/blood , Practice Guidelines as Topic , Refeeding Syndrome/blood , Refeeding Syndrome/etiology , Refeeding Syndrome/physiopathology , Refeeding Syndrome/prevention & control , Severity of Illness Index
13.
Zentralbl Chir ; 140(4): 407-16, 2015 Aug.
Article in German | MEDLINE | ID: mdl-23824622

ABSTRACT

The increasing prevalence of morbid obesity in Germany is associated with an increasing number of metabolic surgical interventions. Short-term surgical and long-term metabolic complications such as nutrient deficiencies can be considered the main risks of metabolic surgery and its restrictive and malabsorbant surgical procedures. The aim of this compact short overview based on a selective literature search and our own clinical experience is to characterise the long-term metabolic complications, which are specific for the various bariatric procedures, and to refine the published guidelines for supplementation. Restrictive bariatric procedures can be associated with well-known surgical problems such as pouch dilatation or band migration, e.g., after gastric banding. After sleeve gastrectomy, emerging reflux disease can become a substantial problem. The most frequent deficiencies after restrictive procedures are related to B-vitamins whereas iron, folate, vitamin B1 and B12 and vitamin D deficiencies are associated with the malabsorptive procedure such as biliopancreatic diversion, duodenal switch and Roux-en-Y gastric bypass. Due to possible metabolic and surgical complications after bariatric surgery, patients need to undergo life-long medical follow-up investigations. The currently available guidelines of German Society of Treatment of Obesity (CAADIP) of DGAV for supplementation should be known and followed, in particular, by the physicians who i) are exceptionally involved in medical care of obese people and ii) do it in full awareness of the obligatory postoperative clinical observation.


Subject(s)
Bariatric Surgery/adverse effects , Deficiency Diseases/diagnosis , Deficiency Diseases/therapy , Nutrition Assessment , Postoperative Complications/diagnosis , Postoperative Complications/therapy , Adolescent , Female , Follow-Up Studies , Germany , Humans , Malabsorption Syndromes/diagnosis , Malabsorption Syndromes/therapy , Male , Nutritional Requirements
14.
J Pediatr ; 164(6): 1432-5, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24657121

ABSTRACT

OBJECTIVES: To evaluate surfactant content and function through the lamellar body count (LBC) and stable microbubble test (SMT) in mechanically ventilated infants with severe acute viral bronchiolitis. STUDY DESIGN: Controlled cross-sectional study of 32 infants receiving mechanical ventilation: 16 with a diagnosis of acute viral bronchiolitis and 16 with normal lungs. Tracheal fluid was collected and LBC was performed in an automated cell counter. Samples were kept frozen and thawed for testing. At the time of analysis, samples were diluted in a dithiothreitol solution, vortexed for 10 seconds, and aspirated by the cell counter. SMT was performed using the Pattle technique. RESULTS: In the bronchiolitis group, the median (IQR) LBC was significantly lower than in the control group: 130,000 (61,250-362,250) vs. 518,000 (180,250-896,000) lamellar bodies/µL; P = .003. Median (IQR) SMT values were also significantly lower in the bronchiolitis group: 10 (2-13) vs. 400 (261-615) microbubbles/mm2; P < .001. CONCLUSIONS: Infants with acute viral bronchiolitis have reduced surfactant content and function. We speculate that these simple tests may be useful to identify infants with bronchiolitis who would benefit from surfactant replacement therapy.


Subject(s)
Bronchiolitis, Viral/diagnosis , Bronchiolitis, Viral/therapy , Deficiency Diseases/diagnosis , Pulmonary Surfactants/analysis , Surface-Active Agents/therapeutic use , Acute Disease , Bronchoalveolar Lavage Fluid/chemistry , Case-Control Studies , Combined Modality Therapy , Critical Care/methods , Cross-Sectional Studies , Deficiency Diseases/therapy , Female , Follow-Up Studies , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Male , Microbubbles , Reference Values , Respiration, Artificial/methods , Risk Assessment , Severity of Illness Index , Statistics, Nonparametric , Survival Rate , Time Factors , Treatment Outcome
15.
J Clin Gastroenterol ; 48(10): 862-5, 2014.
Article in English | MEDLINE | ID: mdl-24583748

ABSTRACT

Malabsorptive bariatric surgery is rapidly becoming a major cause of copper deficiency given the increasing prevalence of these procedures for morbid obesity. Acquired copper deficiency can present with clinically significant hematologic and neurological manifestations. Although hematologic manifestations of copper deficiency are rapidly reversible, significant neurological improvement after copper supplementation therapy is unusual and many patients remain debilitated and may only experience, at best, stabilization of the neurological manifestations. Here we present a case of an undiagnosed copper deficiency several years after bariatric gastric bypass surgery, in a patient who concomitantly used zinc-containing denture cream for several years, associated with anemia, neutropenia, myelopathy, respiratory failure, and bilateral optic neuropathy, which caused major vision loss. This patient was also a heterozygote carrier of the 5,10-methylenetetrahydrofolate reductase A1298C gene polymorphism, which may affect copper metabolism. Intravenous copper repletion resulted in rapid correction of hematologic indices. However, neurological manifestations, including vision loss responded only modestly to copper supplementation, despite achieving normal blood copper concentrations. Clinicians should consider copper deficiency in patients at risk, as in this case, as a delayed diagnosis can lead to irreversible disability due to neurological manifestations.


Subject(s)
Anemia/etiology , Copper/deficiency , Deficiency Diseases/etiology , Gastric Bypass/adverse effects , Neutropenia/etiology , Obesity, Morbid/surgery , Optic Nerve Diseases/etiology , Spinal Cord Diseases/etiology , Anemia/blood , Anemia/diagnosis , Anemia/therapy , Copper/blood , Copper/therapeutic use , Deficiency Diseases/blood , Deficiency Diseases/diagnosis , Deficiency Diseases/genetics , Deficiency Diseases/therapy , Female , Humans , Methylenetetrahydrofolate Reductase (NADPH2)/genetics , Methylenetetrahydrofolate Reductase (NADPH2)/metabolism , Middle Aged , Neutropenia/blood , Neutropenia/diagnosis , Neutropenia/therapy , Optic Nerve Diseases/blood , Optic Nerve Diseases/diagnosis , Optic Nerve Diseases/therapy , Polymorphism, Genetic , Risk Factors , Spinal Cord Diseases/blood , Spinal Cord Diseases/diagnosis , Spinal Cord Diseases/therapy , Time Factors , Treatment Outcome
16.
Public Health Nutr ; 17(9): 2138-45, 2014 Sep.
Article in English | MEDLINE | ID: mdl-23930984

ABSTRACT

OBJECTIVE: To describe the cost of diarrhoeal illness in children aged 6-24 months in a rural South African community and to determine the threshold prevalence of stunting at which universal Zn plus vitamin A supplementation (VAZ) would be more cost-effective than vitamin A alone (VA) in preventing diarrhoea. DESIGN: We conducted a cost analysis using primary and secondary data sources. Using simulations we examined incremental costs of VAZ relative to VA while varying stunting prevalence. SETTING: Data on efficacy and societal costs were largely from a South African trial. Secondary data were from local and international published sources. SUBJECTS: The trial included children aged 6-24 months. The secondary data sources were a South African health economics survey and the WHO-CHOICE (CHOosing Interventions that are Cost Effective) database. RESULTS: In the trial, stunted children supplemented with VAZ had 2·04 episodes (95 % CI 1·37, 3·05) of diarrhoea per child-year compared with 3·92 episodes (95 % CI 3·02, 5·09) in the VA arm. Average cost of illness was $Int 7·80 per episode (10th, 90th centile: $Int 0·28, $Int 15·63), assuming a minimum standard of care (oral rehydration and 14 d of therapeutic Zn). In simulation scenarios universal VAZ had low incremental costs or became cost-saving relative to VA when the prevalence of stunting was close to 20 %. Incremental cost-effectiveness ratios were sensitive to the cost of intervention and coverage levels. CONCLUSIONS: This simulation suggests that universal VAZ would be cost-effective at current levels of stunting in parts of South Africa. This requires further validation under actual programmatic conditions.


Subject(s)
Deficiency Diseases/therapy , Diarrhea, Infantile/prevention & control , Dietary Supplements , Rural Health , Zinc/therapeutic use , Child Development , Cohort Studies , Combined Modality Therapy/economics , Computer Simulation , Cost Savings , Cost-Benefit Analysis , Databases, Factual , Deficiency Diseases/epidemiology , Deficiency Diseases/physiopathology , Diarrhea, Infantile/economics , Diarrhea, Infantile/ethnology , Diarrhea, Infantile/etiology , Dietary Supplements/economics , Female , Growth Disorders/economics , Growth Disorders/ethnology , Growth Disorders/etiology , Growth Disorders/prevention & control , Health Care Costs , Health Care Surveys , Humans , Incidence , Infant , Infant Nutritional Physiological Phenomena/economics , Infant Nutritional Physiological Phenomena/ethnology , Male , Rural Health/economics , Rural Health/ethnology , South Africa/epidemiology , Vitamin A/economics , Vitamin A/therapeutic use , World Health Organization , Zinc/economics
17.
Orv Hetil ; 155(51): 2041-7, 2014 Dec 21.
Article in Hungarian | MEDLINE | ID: mdl-25497154

ABSTRACT

Neurological diseases and nutrition are in complex relationship. In the first part of this review the nutritional consequences of acute neurological diseases is presented, with special emphasis on traumatic injuries of the nervous system and stroke. Nutritional therapy of these patients is described in detail. In addition, chronic, degenerative neurological pathological conditions are also discussed, including nutritional consequences and possibilities of therapy. Some ethical and legal issues are also considered. The second part of this review article describes neurological consequences of nutritional problems, both deficits of macro- and micronutrients and toxic effects.


Subject(s)
Central Nervous System Diseases/complications , Central Nervous System Diseases/therapy , Malnutrition/etiology , Malnutrition/therapy , Nutrition Therapy/methods , Acute Disease , Alcoholic Neuropathy/therapy , Alzheimer Disease/complications , Amyotrophic Lateral Sclerosis/complications , Brain Injuries/complications , Central Nervous System Diseases/etiology , Chronic Disease , Deficiency Diseases/etiology , Deficiency Diseases/therapy , Enteral Nutrition , Humans , Malnutrition/complications , Micronutrients/administration & dosage , Multiple Sclerosis/complications , Nutritional Status , Parenteral Nutrition , Parkinson Disease/complications , Spinal Cord Injuries/complications , Stroke/complications
18.
Ann Surg ; 258(6): 964-9, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23324857

ABSTRACT

OBJECTIVE: Anemia after gastrectomy is commonly neglected by clinicians despite being an important and frequent long-term metabolic sequela. We hypothesized that the incidence and timing of the occurrence of iron deficiency after gastrectomy is closely associated with the extent of gastrectomy and the reconstruction method, and we investigated the treatment outcomes of iron supplementation to understand iron metabolism and determine the optimal reconstruction method after gastrectomy. PATIENTS AND METHODS: Using a prospective gastric cancer database, we identified 381 patients with early gastric cancer with complete hematologic parameters who underwent gastrectomy between January 2004 and May 2008. Kaplan-Meier methods, Cox regression, and logistic regression were used to evaluate the associations of the extent of gastrectomy and reconstruction method with iron metabolism. RESULTS: The prevalence of iron deficiency 3 years after gastrectomy was 69.1%, and iron-deficiency anemia was observed in 31.0% of patients. Iron deficiency developed in 64.8% and 90.5% of patients after distal gastrectomy and total gastrectomy within 3 years after surgery (P < 0.0001), respectively. Iron deficiency was significantly more frequent in women than in men (P < 0.0001) and after gastrojejunostomy than after gastroduodenostomy (P < 0.0001). Serum ferritin levels were different according to the extent of gastrectomy and reconstruction method. The proportion of patients treated for iron-deficiency anemia was also significantly different according to the extent of gastrectomy (P = 0.020). CONCLUSIONS: Iron deficiency occurs in most patients with gastric cancer after gastrectomy, and its incidence was different according to the extent of gastrectomy and reconstruction method. To improve iron metabolism after distal gastrectomy, gastroduodenostomy would be the method of reconstruction whenever possible.


Subject(s)
Gastrectomy/adverse effects , Iron Deficiencies , Iron/metabolism , Stomach Neoplasms/surgery , Anemia, Iron-Deficiency/epidemiology , Anemia, Iron-Deficiency/etiology , Anemia, Iron-Deficiency/therapy , Deficiency Diseases/epidemiology , Deficiency Diseases/etiology , Deficiency Diseases/therapy , Dietary Supplements , Digestive System Surgical Procedures/methods , Female , Gastrectomy/methods , Humans , Incidence , Iron/administration & dosage , Male , Middle Aged , Prospective Studies
19.
Prev Med ; 57(1): 26-30, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23541517

ABSTRACT

INTRODUCTION: In order to address population-level mild iodine deficiency in Australia, a mandatory iodine fortification programme of salt used in bread was introduced in late 2009. METHODS: A before-after study was conducted to assess changes in median urinary iodine concentration (MUIC) measurements, according to supplement use, in convenience samples of pregnant women attending a public antenatal clinic in a regional area of New South Wales, Australia in 2008 (n=139), 2011 (n=147) and 2012 (n=114). Knowledge and practices related to iodine nutrition were investigated in 2012, using self-administered questionnaires. RESULTS: The mild iodine deficiency confirmed pre-fortification (MUIC (IQR)=87.5 (62-123.5; n=110)) has steadily improved to 145.5 µg/L (91-252) in 2011 (n=106) and 166 (97-237) in 2012 (n=95) (sufficiency ≥ 150 µg/L). However, only women taking supplements containing iodine had MUIC indicative of sufficiency in both years surveyed post fortification (2011: 178 µg/L vs. 109 µg/L, P<0.001; 2012: 202 µg/L vs. 124 µg/L, P<0.05). Despite bread being the vehicle for iodine fortification, dairy foods remained major contributors to total iodine intake (58%). Overall knowledge regarding health implications of iodine deficiency was poor. CONCLUSIONS: Iodine status of women has improved since the introduction of mandatory iodine fortification; however supplementation is indicated during pregnancy.


Subject(s)
Deficiency Diseases/therapy , Food, Fortified , Health Knowledge, Attitudes, Practice , Iodine/administration & dosage , Trace Elements/administration & dosage , Adolescent , Adult , Female , Humans , Iodine/deficiency , Iodine/urine , Mandatory Programs , Middle Aged , New South Wales , Pregnancy , Program Evaluation , Surveys and Questionnaires , Trace Elements/deficiency , Young Adult
20.
J Am Acad Dermatol ; 69(4): 616-624.e1, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23688650

ABSTRACT

Zinc is a trace element essential to the gastrointestinal, immune, integumentary, reproductive, and central nervous systems. Zinc deficiency is prevalent in many areas of the world and is a diagnostically challenging condition. Cutaneous manifestations typically occur in moderate to severe zinc deficiency and present as alopecia and dermatitis in the perioral, acral, and perineal regions. Zinc deficiency is a potentially fatal disease process. The aim of this review is to focus on the cutaneous manifestations, diagnosis, and treatment of zinc deficiency in children, and to propose an etiologic classification system.


Subject(s)
Deficiency Diseases/diagnosis , Deficiency Diseases/therapy , Dietary Supplements , Zinc/deficiency , Acrodermatitis/etiology , Acrodermatitis/physiopathology , Acrodermatitis/therapy , Alopecia/etiology , Alopecia/physiopathology , Alopecia/therapy , Child , Child, Preschool , Deficiency Diseases/mortality , Dermatitis/etiology , Dermatitis/physiopathology , Dermatitis/therapy , Female , Humans , Infant , Male , Malnutrition/complications , Pediatrics , Prognosis , Risk Assessment , Survival Rate , Treatment Outcome , Zinc/metabolism
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