| Literature DB >> 34835934 |
Dominika Guzek1, Aleksandra Kołota2, Katarzyna Lachowicz2, Dominika Skolmowska2, Małgorzata Stachoń2, Dominika Głąbska2.
Abstract
Diabetes is associated with a number of mental health consequences, including enhanced risk of depression and anxiety, as well as decreased quality of life, and vitamin D deficiency is considered to be one of the factors that influence these outcomes in diabetic patients. The aim of the present study was to conduct a systematic review of the literature presenting the data regarding the influence of vitamin D supplementation on mental health in diabetic adults. This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and registered in the International Prospective Register of Systematic Reviews (PROSPERO) database (Registration number CRD42020155779). A systematic search of the PubMed and Web of Science databases was performed, and the intervention studies published until September 2021 were included in the review. The human studies were included if an adult sample of diabetic individuals received vitamin D supplementation during the intervention and its effect on any mental health aspect was assessed, but studies presenting the influence of combined supplementation of multiple nutrients were excluded. After removing duplicate records, a total of 8514 publications were screened and assessed independently by two researchers, based on their title, abstract, and full text. Finally, six studies were included in the current systematic review, and the risk of bias was evaluated using the Newcastle-Ottawa Scale (NOS). The included studies analyzed the influence of a specific dose of vitamin D, or different doses of vitamin D, or compared the results of supplementation with a specific dose of vitamin D against the placebo group. The supplementation was performed for at least 12 weeks. The mental health outcomes analyzed in these studies included health-related quality of life, depression, anxiety, stress, and general mental health status of adult diabetic patients. The results of the majority of the studies confirmed the positive influence of vitamin D supplementation on the mental health of diabetic individuals. Those studies that analyzed the influence of vitamin D supplementation on depression and anxiety established the beneficial effect of the vitamin. In some studies, the influence of vitamin D supplementation on the health-related quality of life was not considered unless combined with mindfulness training. However, it must be emphasized that different dosage regimens and intervention periods were followed in the reviewed studies, and only a small number of studies were randomized against placebo, which should be considered as a limitation of the present study. The findings of the conducted systematic review demonstrated the positive influence of vitamin D supplementation on the mental health of diabetic patients, which was proved for anxiety and depression, but in the case of health-related quality of life, the positive effect was observed only when the intervention included mindfulness training. These outcomes suggest that supplementation should be recommended to improve the vitamin D status and the mental health of patients in this group.Entities:
Keywords: anxiety; cholecalciferol; depression; diabetes; health-related quality of life (HRQOL); mental health; stress; supplementation; vitamin D
Mesh:
Substances:
Year: 2021 PMID: 34835934 PMCID: PMC8625262 DOI: 10.3390/nu13113678
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717
The inclusion and exclusion criteria for the systematic review.
| Criteria | |
|---|---|
| Inclusion |
studies published in peer-reviewed journals; full text articles published in English; studied group of adults; diabetes mellitus diagnosed in the studied population; supplementation of vitamin D applied; assessed outcome including any component of mental health assessed while using any method (either subjective or objective) |
| Exclusion |
animal model studies; studies conducted in participants with any intellectual disabilities; studies conducted in participants with any eating disorders; studies conducted in participants with any neurological disorders (Alzheimer’s disease, epilepsy, etc.); studies including assessment of combined supplementation of multiple nutrients. |
Figure 1The identification, screening, eligibility, and inclusion within the systematic review.
The basic details of the studies included to the systematic review.
| Ref. | Authors, Year | Design of the Study | Country/Location | Studied Group | Time |
|---|---|---|---|---|---|
| [ | Westra et al. 2016 | Randomized, double-blind, placebo-controlled trial—SUNNY trial (StUdy the effect of vitamiN D supplemeNtation on glYcaemic control in type 2 DM) | Netherlands/in and around the city of Alkmaar | Adults with type 2 diabetes mellitus derived from general practitioners | July 2012 to April 2013 |
| [ | Mager et al., 2017 | Open-label randomized clinical trial | Canada/Northern Alberta | Adults with diabetes mellitus and chronic kidney disease from two clinics (Diabetes Nephropathy Prevention Clinic and Renal Insufficiency Clinic in the Northern Alberta) | 2011 to 2014 |
| [ | Penckofer et al., 2017 | Open-label, proof-of-concept study—Sunshine Study | United States of America/Chicago * | Women with type 2 diabetes mellitus and significant depressive symptomology | From October 2009 to May 2012 * |
| [ | Fazelian et al., 2019 | Randomized double-blind placebo-controlled clinical trial | Iran/Shahr-e-Kord | Women with type 2 diabetes mellitus, vitamin D deficiency, and anxiety recruited from Shahr-e-Kord Diabetes Clinic | Not specified |
| [ | Omidian et al., 2019 | Randomized placebo-controlled double-blind clinical trial | Iran | Patients with type 2 diabetes mellitus and mild to moderate depressive symptoms | Inclusion from October 2017 to May 2018 and follow up for 12 weeks |
| [ | Davoudi et al., 2021 | Randomized placebo-controlled clinical trial | Iran/Kermanshah | Patients with painful diabetic neuropathy and vitamin D deficiency referred to Beheshti hospital, Kermanshah, Iran | September 2019 to January 2020 |
* data provided on request; DM—diabetes mellitus.
The basic characteristics of the participants of the studies included in the systematic review.
| Ref. | Number of Participants (Female Participants) | Inclusion Criteria | Exclusion Criteria |
|---|---|---|---|
| [ | 187 (62) | Inclusion: aged ≥18 years; type 2 diabetes mellitus; treated with lifestyle advice, metformin, and/or sulfonylurea derivatives; serum HbA1c stable and ≤8.0% for the last three months without recent changes in hypoglycemic agents | Exclusion: insulin therapy; impaired renal function (GFR < 30 mL/min/1.73 m2); any granuloma forming disorder; hypercalcemia (serum calcium > 2.65 nmol/L); serum 25-hydroxyvitamin D (25(OH) D) <15 nmol/L or >150 nmol/L; urolithiasis; psychiatric treatment for schizophrenia; organic mental disorder or bipolar disorder currently or in the past; insufficient knowledge of the Dutch language; substance abuse (other than nicotine); increase in HbA1c to >8.5% within the study; hypersensitivity to cholecalciferol or placebo within the study; onset of urolithiasis within the study; any change in antidiabetic medication within the study; serum 25(OH)D <15 or >250 nmol/L within the study; taking vitamin D supplements other than planned within the study |
| [ | 120 (44) | Inclusion: aged 18–80 years; type 1 or type 2 diabetes mellitus; stages 1–4 of chronic kidney disease (GFR 15–89 mL/min/1.73 m2) | Exclusion: co-morbid conditions known to affect vitamin D metabolism including gastrointestinal, liver, rheumatoid, or bone disorders (e.g., hyperthyroidism, untreated celiac disease, cancer, Paget’s disease, sarcoidosis, malabsorption); severe, permanent vision impairment; pregnancy; body mass of >136 kg; drug therapy known to interfere with vitamin D (e.g., oral glucocorticoids, cholestyramine, colestipol, mineral oil, Orlistat, digoxin); applying other forms of active vitamin D metabolites (e.g., calcitriol, vitamin D2); dialysis therapy or being on a kidney transplant list; pre-existing hypercalcemia (>2.75 mmol/L), hyperphosphatemia (>2.0 mmol/L), severe secondary hyperparathyroidism (PTH > 66 pmol/L), and serum 25(OH)D > 200 nmol/L; serum 25(OH)D < 37.5 nmol/L at time of screening; undergoing strict heavy exercise for weight control; using sunscreen lotion on a daily basis |
| [ | 50 (50) | Inclusion: women; aged ≥18; medically stable type 2 diabetes mellitus with HbA1c ≤9%; elevated depressive symptoms measured using the CES-D Scale; average score of ≥16 on the CES-D Scale from two screenings (phone and baseline) within 4 weeks of each screening | Exclusion: taking vitamin D supplementation during 2 months prior to enrolment; vitamin D levels ≥80 nmol/L; malabsorption problems (e.g., Crohn’s disease, celiac sprue) and/or bariatric surgery; hypercalcemia; severe complications of diabetes (e.g., amputation, blindness); low thyroid function; pregnancy; active suicidal ideation; history of bipolar depression; psychotic disorders; current alcohol or substance disorders |
| [ | 51 (51) | Inclusion: women; aged 20–60 years; diagnosis of type 2 diabetes mellitus based on the World Health Organization guidelines; mild, moderate, or severe anxiety; vitamin D deficiency or insufficiency (serum 25(OH)D of 25–75 nmol/L) | Exclusion: neurological or psychiatric disorders; taking any medications for depression or vitamin D/multivitamin supplements during the last 4 months; alcohol consumption; pregnancy; lactation |
| [ | 66 (27) | Inclusion: aged 30–60 years; type 2 diabetes mellitus; BMI 20–30 kg/m2; willingness to maintain the current diet, physical activity, and lifestyle for 3 months | Exclusion: receiving herbal products or dietary supplements for 3 months before and throughout the intervention; major depressive disorder and taking antidepressants; chronic kidney diseases; hepatobiliary diseases; gastrointestinal diseases; taking drugs that interact with vitamin D such as anticonvulsant drugs; using insulin or thiazolidinediones or anti-obesity drugs; pregnancy; lactation; any changes in the type or dosage of medications during the study; lack of adherence to the trial based on refusing to consume at least 90% of recommended treatments |
| [ | 204 (92) | Inclusion: age 20–70 years; type 2 diabetes mellitus; neuropathy; vitamin D insufficiency or deficiency (serum 25(OH)D of 25–75 nmol/L) | Exclusion: major co-morbid disease (e.g., coronary heart disease, psychiatric or neurological diseases); taking vitamin D or any multivitamins during the last three months; using any substance and drinking alcohol; pregnancy; more than one absence in mindfulness sessions |
* data provided on request; BMI—body mass index; CES-D—Center for Epidemiologic Studies Depression Scale; GFR—glomerular filtration rate; HbA1c—hemoglobin A1c (glycated hemoglobin); PTH—parathyroid hormone (parathormone).
The basic description of the exposure and outcomes within the studies included to the systematic review.
| Ref. | Vitamin D Assessment | Vitamin D Supplementation | Mental Health Component | Psychological Measure |
|---|---|---|---|---|
| [ | 25(OH) vitamin D level in blood | 1250 µg/month vs. placebo for 6 months | Health-related quality of life (HRQOL) | The Dutch version of the Short Form 36 (SF-36) |
| [ | 25(OH) and 1,25(OH)2 vitamin D level in blood, | 50 µg/day vs. 1000 µg/month for 6 months | Health-related quality of life (HRQOL) | Short Form 36 (SF-36) |
| [ | 25(OH) vitamin D level in blood | 1250 µg/week for 6 months |
depression anxiety mental health status |
Center for Epidemiologic Studies Depression (CES-D) Scale; Patient Health Questionnaire-9 (PHQ-9) State–Trait Anxiety Inventory (STAI) Short Form 12 (SF-12) |
| [ | 25(OH) vitamin D level in blood, | 1250 µg/2 weeks vs. placebo for 16 weeks | Depression, anxiety, stress | Depression, Anxiety, and Stress Scales (DASS-21) questionnaire |
| [ | 25(OH) vitamin D level in blood | 100 µg/day vs. placebo for 3 months | Depression | Persian version of Beck Depression Inventory-II (BDI-II-PERSIAN) |
| [ | 25(OH) vitamin D level in blood, | 100 µg/day vs. placebo for 12 weeks | Health-related quality of life (HRQOL) | The Neuropathy Specific Quality of Life questionnaire (NeuroQol) |
The findings presented within the studies included to the systematic review.
| Ref. | Observations | Conclusions |
|---|---|---|
| [ | A small significant difference (adjusted β: −8.90; 95% CI: −17.16 to −0.65) between both groups was seen concerning the SF-36 domain role limitations due to physical problems in disadvantage of the vitamin D group. | Six months of vitamin D supplementation did not improve HRQOL in non-vitamin D-deficient people with type 2 diabetes mellitus managed on oral antidiabetic therapy. |
| [ | No significant differences over six months between groups were observed in quality of life measures ( | Daily (50 µg/day) and monthly (1000 µg/month) vitamin D3 supplementation for six months in adults with diabetes mellitus and CKD was safe, and resulted in equivalent adherence and improvements in overall vitamin D status, but only modest changes in quality of life (no significant changes). |
| [ | There was a significant decrease in depression (CES-D and PHQ-9, | This proof-of-concept study found that weekly administration of 1250 µg of vitamin D in women with type 2 diabetes mellitus who had significant depressive symptoms and low 25(OH)D levels had an improvement in depression, anxiety, and mental health outcomes. |
| [ | Anxiety score changes were significantly lower in vitamin D group than the controls ( | Vitamin D supplementation can improve mood status in female diabetics with anxiety and vitamin D deficiency. |
| [ | BDI-II scores decreased from 15.2 ± 9.6 to 9.8 ± 7.2 ( | Supplementation of vitamin D in type 2 diabetes mellitus patients may protect patients against the onset of major depressive disorder. |
| [ | At the end-of-treatment, results showed improvement in all groups except the “placebo only” group for outcome variables. There was no difference between vitamin D and mindfulness groups (within and not combined with placebo) in posttest. However, “vitamin D + mindfulness” has a greater improvement rather than vitamin D and mindfulness groups ( | Combining vitamin D and mindfulness training can reduce pain severity and pain-related disability, so with these changes, patients experience improvement in their quality of life. |
BDI-II—Beck Depression Inventory-II; CES-D—Center for Epidemiologic Studies Depression; CI—confidence interval; CKD—chronic kidney disease; HRQOL—Health-related quality of life; PHQ-9—Patient Health Questionnaire-9; SF-12—Short Form 12; SF-36—Short Form 36.
The summary of findings presenting association between vitamin D supplementation and mental health in diabetic adults, accompanied by the Newcastle–Ottawa Scale (NOS) score for the studies included in the systematic review.
| Ref. | Association between Vitamin D Supplementation and Mental Health in Diabetic Adults | Quality | ||
|---|---|---|---|---|
| Studied Outcome | Supporting/Not Supporting a | Randomization against Placebo | Newcastle–Ottawa Scale (NOS) Score b | |
| [ | Health-related quality of life (HRQOL) | Not supporting | + | 9 |
| [ | Health-related quality of life (HRQOL) | Not supporting | - | 9 |
| [ | Depression, anxiety, mental health status | Supporting | - | 7 |
| [ | Depression, anxiety, stress | Supporting | + | 8 |
| [ | Depression | Supporting | + | 6 |
| [ | Health-related quality of life (HRQOL) | Supporting (for vitamin D combined with mindfulness training) | + | 7 |
a Supporting—positive influence of vitamin D supplementation on mental health; not supporting—no positive influence of applied vitamin D supplementation on mental health; b the Newcastle–Ottawa Scale (NOS) score attributed to following categories: very high risk of bias (0–3 NOS points), high risk of bias (4–6 NOS points), low risk of bias (7–9 NOS points) [24].