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1.
J Community Psychol ; 49(6): 1838-1871, 2021 08.
Article in English | MEDLINE | ID: mdl-34125969

ABSTRACT

AIMS: Gatekeeper training (GKT) is an important suicide prevention strategy. Studies have evaluated the effectiveness of GKT in different populations, often neglecting family and friends who play a vital role in caring for people with suicide risk. This review evaluated GKT programs targeting family and friends to determine their effectiveness in this specific population. METHODS: Academic databases were searched for studies on GKT programs. Programs involving family and friends caring for people with suicide risk were assessed for any impact on knowledge, self-efficacy, attitudes, and suicide prevention skills. RESULTS: Seventeen studies were reviewed. GKT showed significant gains on outcomes of interest. Three studies targeted family and friends, with one involving them in program creation and conduction and another adjusting the program after their input. CONCLUSIONS: GKT programs have potentially positive effects on family and friends caring for people with suicide risk. Few programs address the specific needs of this group, and programs adapted specifically for them are scarce. Future program development recommendations are discussed.


Subject(s)
Friends , Suicide Prevention , Humans , Program Development , Self Efficacy
2.
Biometals ; 26(1): 133-40, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23255060

ABSTRACT

Zinc (Zn) deficiency is a problem world-wide. Current methods for assessing Zn status are limited to measuring plasma or serum Zn within populations suspected of deficiency. Despite the high prevalence of Zn deficiency in the human population there are no methods currently available for sensitively assessing Zn status among individuals. The purpose of this research was to utilize a proteomic approach using two-dimensional gel electrophoresis (2DE) and mass spectrometry to identify protein biomarkers that were sensitive to changes in dietary Zn levels in humans. Proteomic analysis was performed in human plasma samples (n = 6) obtained from healthy adult male subjects that completed a dietary Zn depletion/repletion protocol, current dietary zinc intake has a greater effect on fractional zinc absorption than does longer term zinc consumption in healthy adult men. Chung et al. (Am J Clin Nutr 87 (5):1224-1229, 2008). After a 13 day Zn acclimatization period where subjects consumed a Zn-adequate diet, the male subjects consumed a marginal Zn-depleted diet for 42 days followed by consumption of a Zn-repleted diet for 28 days. The samples at baseline, end of depletion and end of repletion were pre-fractionated through immuno-affinity columns to remove 14 highly abundant proteins, and each fraction separated by 2DE. Following staining by colloidal Coomassie blue and densitometric analysis, three proteins were identified by mass spectrometry as affected by changes in dietary Zn. Fibrin ß and chain E, fragment double D were observed in the plasma protein fraction that remained bound to the immunoaffinity column. An unnamed protein that was related to immunoglobulins was observed in the immunodepleted plasma fraction. Fibrin ß increased two-fold following the Zn depletion period and decreased to baseline values following the Zn repletion period; this protein may serve as a viable biomarker for Zn status in the future.


Subject(s)
Fibrin/metabolism , Proteome/metabolism , Zinc/deficiency , Adult , Blood Proteins/metabolism , Diet , Hemostasis , Humans , Male , Middle Aged , Zinc/blood
3.
Pediatrics ; 130(2): e408-14, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22778306

ABSTRACT

In this review, we explain how the US Food and Drug Administration (FDA) used its evidence-based review system to evaluate the scientific evidence for a qualified health claim for 100% whey-protein partially hydrolyzed infant formula (W-PHF) and reduced risk of atopic dermatitis (AD). The labeling of health claims, including qualified health claims, on conventional foods and dietary supplements require premarket approval by the FDA. Health claims characterize the relationship between a substance (food or food component) and disease (eg, cancer or cardiovascular disease) or health-related condition (eg, hypertension). To determine whether sufficient evidence exists to support the qualified health claim, the FDA evaluated human intervention studies that evaluated the role of W-PHF in reducing the risk of AD. The FDA concluded there is little to very little evidence, respectively, to support a qualified health claim concerning the relationship between intake of W-PHF and a reduced risk of AD in partially breastfed and exclusively formula-fed infants throughout the first year after birth and up to 3 years of age. In addition, the FDA required a warning statement be displayed along with the health claim to indicate to consumers that partially hydrolyzed infant formulas are not hypoallergenic and should not be fed to infants who are allergic to milk or to infants with existing milk allergy symptoms.


Subject(s)
Dermatitis, Atopic/prevention & control , Infant Formula , Milk Proteins , Protein Hydrolysates , United States Food and Drug Administration , Child, Preschool , Controlled Clinical Trials as Topic , Dermatitis, Atopic/genetics , Endpoint Determination , Evidence-Based Medicine , Food Labeling , Food Safety , Genetic Predisposition to Disease/genetics , Humans , Infant , Infant, Newborn , Milk Proteins/adverse effects , Protein Hydrolysates/adverse effects , Randomized Controlled Trials as Topic , United States , Whey Proteins
4.
Am J Clin Nutr ; 90(2): 321-8, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19515738

ABSTRACT

BACKGROUND: Zinc plays an important role in antioxidant defense and the maintenance of cellular DNA integrity. However, no experimental human studies have been performed to examine the role of zinc status on DNA damage. OBJECTIVE: We evaluated the effects of dietary zinc depletion and repletion on DNA strand breaks, oxidative stress, and antioxidant defenses in healthy men. DESIGN: Nine healthy men with reported mean daily zinc intakes >11 mg/d were recruited. Subjects completed 3 consecutive dietary periods: baseline (days 1 to 13; 11 mg Zn/d), zinc depletion (days 14 to 55; 0.6 mg Zn/d for 1 wk and 4 mg Zn/d for 5 wk), and zinc repletion (days 56 to 83; 11 mg Zn/d for 4 wk with 20 mg supplemental Zn for first 7 d). Blood samples were collected on days 1, 13, 35, 55, and 83. DNA damage in peripheral blood cells, plasma oxidative stress, and antioxidant defense biomarkers were assessed. RESULTS: Dietary zinc depletion (6 wk) was associated with increased DNA strand breaks in peripheral blood cells (day 13 compared with day 55; P < 0.05), changes that were ameliorated by zinc repletion (day 55 compared with day 83; P < 0.05). Plasma zinc concentrations were negatively correlated with DNA strand breaks (r = -0.60, P = 0.006) during the zinc-depletion period. Plasma alpha- and gamma-tocopherol concentrations, plasma total antioxidant capacity, and erythrocyte superoxide dismutase activity did not change significantly, and plasma F(2)-isoprostanes were unaffected by dietary period. CONCLUSIONS: Changes in dietary zinc intake affected DNA single-strand breaks. Zinc appears to be a critical factor for maintaining DNA integrity in humans.


Subject(s)
DNA Breaks/drug effects , DNA Damage/drug effects , Nutritional Status , Oxidative Stress/drug effects , Zinc/deficiency , Zinc/pharmacology , Adult , Antioxidants/metabolism , Biomarkers/blood , Biomarkers/metabolism , Comet Assay , DNA Breaks, Single-Stranded/drug effects , F2-Isoprostanes/blood , Humans , Male , Middle Aged , Oxidation-Reduction , Superoxide Dismutase/metabolism , Tocopherols/blood , Trace Elements/deficiency , Trace Elements/pharmacology , Young Adult , Zinc/metabolism
5.
Am J Clin Nutr ; 87(5): 1224-9, 2008 May.
Article in English | MEDLINE | ID: mdl-18469243

ABSTRACT

BACKGROUND: No studies have examined the independent effects of current and longer-term dietary zinc intakes on zinc absorption. OBJECTIVE: We determined the effects of current compared with longer-term zinc intake on fractional zinc absorption (FZA). DESIGN: We studied 9 men whose usual zinc intakes were >11 mg/d. FZA was measured at baseline, depletion (0.6 mg Zn/d for 1 wk and 4 mg Zn/d for 5 wk), and repletion (11 mg Zn/d for 4 wk with 20 mg supplemental Zn/d for first 7 d). During 2 successive days after each dietary period, subjects consumed either adequate-zinc meals (11 mg Zn/d) with a zinc stable isotope tracer for 1 d, followed by low-zinc meals (4 mg Zn/d) with zinc tracer, or vice versa. Five days after oral dosing, a zinc tracer was infused intravenously. FZA was measured with the use of a modified double isotope tracer ratio method with urine samples collected on days 5-7 and 10-12 of absorption studies. RESULTS: Plasma and urinary zinc did not vary by dietary period. Mean FZA was greater from low-zinc meals than from adequate-zinc meals (60.9% +/- 13.8% compared with 36.1% +/- 8.9%; P < 0.0001), whereas mean total absorbed zinc was greater from adequate-zinc meals than from low-zinc meals (3.60 +/- 0.91 compared with 2.48 +/- 0.56; P < 0.0001), regardless of the longer-term dietary period. CONCLUSIONS: FZA was inversely related to current zinc intake, but there was no detectable effect of longer-term dietary zinc. If longer- term zinc intake does modify FZA, such changes are smaller than those caused by current zinc intake, or they occur only after more severe zinc depletion.


Subject(s)
Diet , Nutritional Status , Zinc/administration & dosage , Zinc/pharmacokinetics , Adult , Biological Availability , Cross-Over Studies , Dose-Response Relationship, Drug , Feeding Behavior , Humans , Indicator Dilution Techniques , Intestinal Absorption/drug effects , Isotope Labeling , Male , Middle Aged , Zinc/blood , Zinc/urine , Zinc Isotopes
6.
J Nutr ; 132(7): 1903-5, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12097667

ABSTRACT

This study determined whether a single 60-mg dose of ferrous sulfate interferes with fractional zinc absorption (FZA) at 7-9 wk of lactation. In a crossover design, 5 exclusively breast-feeding women were given either a single 60-mg iron supplement or no supplement. FZA was measured by analyzing zinc stable isotope tracers ((70)Zn and (67)Zn) in urine samples collected for 7 d after isotope dosing. A 0.7-micromol intravenous (IV) infusion of (70)Zn as ZnCl(2) in saline was followed by a 0.03-mmol oral dose of (67)Zn as ZnCl(2) given with a standardized meal. After a 7-d wash-out period, the supplement given was reversed and a second FZA measurement was taken. FZA was calculated from isotopic enrichments in urine measured by inductively coupled plasma mass spectrometry. Hemoglobin, plasma ferritin and transferrin receptor, and plasma 5'-nucleotidase, plasma zinc and erythrocyte zinc did not differ before the two measurements of zinc absorption. When women were given a single iron supplement, FZA was significantly lower, 21.7 +/- 1.7% compared with 26.9 +/- 2.6% when no supplement was given (P = 0.032). A single 60-mg iron dose significantly decreases FZA during early lactation.


Subject(s)
Ferrous Compounds/administration & dosage , Lactation/metabolism , Zinc/pharmacokinetics , Absorption/drug effects , Adult , Cross-Over Studies , Dose-Response Relationship, Drug , Female , Ferrous Compounds/pharmacology , Humans , Pregnancy , Zinc/urine
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