BF: Dietary Factors, Breast Milk and Infant Outcomes (2008)
Eilander A, Hundscheid DC, Osendarp SJ, Transler C, Zock PL. Effects of n-3 long chain polyunsaturated fatty acid supplementation on visual and cognitive development throughout childhood: A review of human studies. Prostaglandins, Leukotrienes and Essential Fatty Acids 2007; 76: 189-203.
PubMed ID: 17376662To evaluate the effect of long chain polyunsaturated fatty acids (LCPUFA) during pregnancy and lactation on visual and cognitive function during infancy and later childhood.
- Randomized controlled trials (include observational studies only if there are less than three trials on a particular topic)
- LCPUFA supplementation lasted at least four weeks
- LCPUFA as sole variable differing between treatment and controls
- Measured visual or cognitive development.
None except not meeting all inclusion criteria.
Database
Literature databases of Web of Science. Search year was not reported.
Search terms
Long chain polyunsaturated fatty acids, docosahexaenoic acid, eicosapentaenoic acid, linolenic acid, arachidonic acid, linoleic acid, omega-3 fatty acids, omega-6 fatty acids" with "infants, children, pre-schoolers, toddlers, complementary feeding, neonates, offspring, babies", with "cognition, development, mental, learning, brain, visual acuity, neurology".
Design
Systematic review.
Meta-analysis methods
No meta-analysis was performed.
Data extraction tools and personnel was not described. No methodological quality assessment for primary studies.
Study characteristics collected include:
- Study year
- Study country of origin
- Number of subjects
- Treatment timing, duration and dose
- Outcome assessment timing and method.
Outcomes collected include:
- Visual development: Retinal function per electroretinography, visual acuity per visual evoked potentials
- Cognitive development: Including Bayley Scales of Infant Development, Kaufman Assessment Battery for Children, Wechsler tests.
- Total number of studies identified from the search: Not reported
- Total number of studies meeting the inclusion criteria: Six
- Location of these studies vary: United Kingdom, Bangladesh, Norway, Australia, Denmark, and United States of America
- Two CRTs studied the effect of supplementation during pregnancy only, one studied supplementation during pregnancy and lactation, and three studied supplementation during lactation only.
Overview of RCTs on effect of omega-3 supplementation in pregnant and lactating women on visual and cognitive development of infants.
Author, Location, Year |
N |
Supplementation to Mothers |
Functional Measurements: Age at Assessment |
Significant Effects of Supplementation |
||
|
Period |
Dose per Day |
|
Functional |
||
|
63 |
Week 15 to delivery |
I: 200mg DHA+36mg |
Flash VEP: Zero to five days |
None |
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|
|
|
C: 400mg oleic acid |
Flash and pattern-reversal VEP: 50, 66 weeks PCA |
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|
|
|
|
|
ERG: zero to seven days |
|
|
|
249 |
Week 25 to delivery |
I: 1,200mg DHA+1,800mg EPA |
BSID: 10 months |
None |
|
|
|
|
C: 2,250mg LA+270mg |
|
|
|
|
341 |
Week 17–19 to three months post-partum |
I: 1,183mg DHA+803mg EPA+160mg LA |
EEG: Two days, three months |
None |
|
|
|
|
C: 8.3mg DHA+4,747mg LA |
FT: 27, 39 weeks |
|
|
|
90 |
Week 17–19 to three months post-partum |
I: 1183 mg DHA+803 mg EPA+160 mg LA |
IQ (K-ABC): Four years |
Positive: IQ 4.1 points higher in I vs. C |
|
|
|
|
C: 8.3 mg DHA+4747 mg LA |
|
|
|
|
52 |
12 weeks post-partum |
I1: 0g DHA |
VEP: 12, 16 weeks |
None |
|
|
|
|
I2: 0.2g DHA |
BSID: One, two year |
|
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|
|
I3: 0.4g DHA |
|
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I4: 0.9g DHA |
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I5: 1.3g DHA |
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|
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Lauritzen Denmark, 2004, 2005 |
97 |
16 weeks post-partum |
I: 1.3g DHA+EPA+DPA |
VEP: Two, Four months |
Positive: MPS intention scores 2.0 points higher in I vs. C in girls |
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|
|
|
C: Olive oil |
Motor function: Two, four, nine months |
Negative: MACI vocabulary comprehension 17 points lower in I vs. C; 33 points lower in I vs. C in boys; sentence complexity 3.0 points lower in I vs. C in boys |
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MPS: Nine months |
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|
|
MACI: 12, 24 months |
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|
|
160 |
Four months post-partum |
I: 200mg DHA |
TAC, VEP: Four, eight months GGM, CLAMS |
Positive: BSID-PDI 8.4 points higher in I vs. C |
|
|
|
|
C: Soy+corn oil |
CAT: 12, 30 months |
|
I, intervention group; C, control group; DHA, docosahexaenoic acid; EPA, eicosapentaenoic acid; LA, linoleic acid; ALA, α-linolenic acid; DPA, docosapentaenoic acid; VEP, visual evoked potential; PCA, post-conceptional age; ERG, electroretinography; BSID, Bayley Scales of Infant Development; EEG, electroencephalogram; FT, Fagan Test of Infant Intelligence, K-ABC, Kaufman Assessment Battery for Children; MPS, Means-end Problem Solving; MACDI, MacArthur Communicative Development Inventories; TAC, Teller Acuity Card procedure; GGM, Gesell Gross Motor; CLAMS, Clinical Linguistic and Auditory Milestone Scale; CAT, Clinical Adaptive Test; IQ, Intelligence Quotient; PDI, Psychomotor Development Index; ND, not determined; HM, human milk.
Maternal DHA supplementation during pregnancy and lactation has no effect on visual development, and may have some positive effects on psychomotor and cognitive development.
Industry: |
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None.
Quality Criteria Checklist: Review Articles
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Relevance Questions | |||
1. | Will the answer if true, have a direct bearing on the health of patients? | Yes | |
2. | Is the outcome or topic something that patients/clients/population groups would care about? | Yes | |
3. | Is the problem addressed in the review one that is relevant to dietetics practice? | Yes | |
4. | Will the information, if true, require a change in practice? | Yes | |
Validity Questions | |||
1. | Was the question for the review clearly focused and appropriate? | Yes | |
2. | Was the search strategy used to locate relevant studies comprehensive? Were the databases searched and the search termsused described? | No | |
3. | Were explicit methods used to select studies to include in the review? Were inclusion/exclusion criteria specified andappropriate? Wereselectionmethods unbiased? | Yes | |
4. | Was there an appraisal of the quality and validity of studies included in the review? Were appraisal methodsspecified,appropriate, andreproducible? | No | |
5. | Were specific treatments/interventions/exposures described? Were treatments similar enough to be combined? | Yes | |
6. | Was the outcome of interest clearly indicated? Were other potential harms and benefits considered? | Yes | |
7. | Were processes for data abstraction, synthesis, and analysis described? Were they applied consistently acrossstudies and groups? Was thereappropriate use of qualitative and/or quantitative synthesis? Was variation in findings among studies analyzed? Were heterogeneity issued considered? If data from studies were aggregated for meta-analysis, was the procedure described? | No | |
8. | Are the results clearly presented in narrative and/or quantitative terms? If summary statistics are used, are levels ofsignificance and/or confidence intervals included? | Yes | |
9. | Are conclusions supported by results with biases and limitations taken into consideration? Are limitations ofthe review identified anddiscussed? | Yes | |
10. | Was bias due to the review's funding or sponsorship unlikely? | ??? | |