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Lutein and Zeaxanthin Supplementation Improves Dynamic Visual and Cognitive Performance in Children: A Randomized, Double-Blind, Parallel, Placebo-Controlled Study.
Parekh, Rajesh; Hammond, Billy R; Chandradhara, Divya.
Affiliation
  • Parekh R; Sanjeevani Netralaya, Infantry Road (Bhagwan Mahaweer Road), Opp. The Hindu, Near Income Tax Office, Bengaluru, 560001, India.
  • Hammond BR; Department of Psychology, UGA Psychology Department, University of Georgia, 125 Baldwin Street, Athens, GA, 30602, USA.
  • Chandradhara D; Bioagile Therapeutics Pvt. Ltd., #2/5, Dahlia Building, 3rd Floor, 80 Feet Road, RMV 2nd Stage, Bengaluru, 560094, India. divya@bioagiletherapeutics.com.
Adv Ther ; 41(4): 1496-1511, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38363462
ABSTRACT

INTRODUCTION:

Supplementation with dietary neuro-pigments lutein (L) and zeaxanthin (Z) has been shown to improve many aspects of visual and cognitive function in adults. In this study, we tested whether a similar intervention could improve such outcomes in preadolescent children.

METHODS:

Sixty children (age range 5-12 years) were randomized in a 21 ratio in this double-blind, placebo-controlled clinical trial. Subjects were supplemented with gummies containing either a combination of 10 mg lutein and 2 mg zeaxanthin (LZ) or placebo for 180 days. Macular pigment optical density (MPOD) was the primary endpoint. The secondary endpoints included serum levels of L and Z, and brain-derived neurotrophic factor (BDNF), critical flicker fusion (CFF), eye strain and fatigue using visual analogue scales (VAS), Children's Sleep Habits Questionnaire-Abbreviated (CSHQ-A), and Creyos Health cognitive domains like attention, focus/concentration, episodic memory and learning, visuospatial working memory, and visuospatial processing speed. Safety was assessed throughout the study on the basis of physical examination, vital signs, clinical laboratory tests, and monitoring of adverse events.

RESULTS:

The LZ group showed significant increases in MPOD at all visits post-supplementation, with significant increases as early as day 42 compared to placebo. The LZ group showed significant increases in serum lutein levels, reduced eye strain and fatigue, and improved cognitive performance (focus, episodic memory and learning, visuospatial working memory) at days 90 and 180 compared to placebo. Further, the LZ group showed significant increases in processing speed (CFF), attention, visuospatial processing, and serum Z and BDNF levels on day 180 compared to placebo. No safety concerns were observed.

CONCLUSIONS:

Supplementing LZ resulted in increased MPOD levels, along with increased serum levels of L, Z, and BDNF. These changes were associated with improved visual and cognitive performances and reduction in eye strain and eye fatigue in the children receiving LZ gummies. The investigational product was safe and well tolerated. TRIAL REGISTRATION http//ctri.nic.in/ Identifier CTRI/2022/05/042364.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lutein / Macular Pigment Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Child / Child, preschool / Humans Language: En Journal: Adv Ther Journal subject: TERAPEUTICA Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lutein / Macular Pigment Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Child / Child, preschool / Humans Language: En Journal: Adv Ther Journal subject: TERAPEUTICA Year: 2024 Document type: Article Affiliation country: