{"id":1018,"date":"2026-03-05T10:03:57","date_gmt":"2026-03-05T10:03:57","guid":{"rendered":"https:\/\/jessicafonteneaunutrition.com\/?p=1018"},"modified":"2026-03-05T10:04:03","modified_gmt":"2026-03-05T10:04:03","slug":"identifying-the-children-who-wont-grow-out-of-eczema","status":"publish","type":"post","link":"https:\/\/jessicafonteneaunutrition.com\/fr\/identifying-the-children-who-wont-grow-out-of-eczema\/","title":{"rendered":"Identifier les enfants qui ne dispara\u00eetront pas de l'ecz\u00e9ma :"},"content":{"rendered":"\n

How Nutrigenomic-Informed Nutrition Changes Outcomes in Paediatric Atopic Dermatitis<\/strong><\/p>\n\n\n\n

In paediatric practice, atopic dermatitis is often framed as a condition of time. Parents are reassured that most children will outgrow their eczema as the immune system matures and the skin barrier strengthens. Epidemiological data broadly supports this narrative, with approximately 80 percent of children experiencing improvement or remission by adolescence\u00b9.<\/p>\n\n\n\n

Yet this framing conceals a clinically significant minority. Around one in five children do not follow this trajectory. Their eczema persists, often intensifies, and frequently becomes the first visible step in the atopic march towards food allergy, asthma, and allergic rhinitis\u00b2. By adolescence, these children are not simply managing eczema, but navigating a cluster of chronic inflammatory conditions that impact sleep, cognition, behaviour, and quality of life.<\/p>\n\n\n\n

The challenge for clinicians is that we have historically lacked reliable tools to identify which children will fall into this high-risk group early enough to intervene. Severity alone is not enough. Nor is symptom suppression sufficient to change long-term outcomes.<\/p>\n\n\n\n

Over the past decade, however, a more predictive picture has begun to emerge, one that reframes persistent eczema not as \u201cbad luck\u201d, but as the visible expression of underlying biological constraints. These constraints are increasingly measurable, and, crucially, many are modifiable through targeted, food-first nutritional intervention.<\/p>\n\n\n\n

A parent-friendly explanation of this topic is available here. [SUBSTACK LINK TO BE INCLUDED HERE] <\/p>\n\n\n\n


From Severity to Biology: Predicting Persistence<\/strong><\/h2>\n\n\n\n

A pivotal shift came with the publication of a prospective cohort study by Lauffer and colleagues, which demonstrated that persistence of paediatric atopic dermatitis can be predicted with over 80 percent accuracy by combining clinical features with circulating protein biomarkers measured at age three\u00b3.<\/p>\n\n\n\n

This work matters because it moves eczema out of the realm of uncertainty. It allows clinicians to distinguish between children whose skin is delayed but developing, and those whose repair systems are fundamentally struggling.<\/p>\n\n\n\n

Four markers emerged as particularly informative.<\/p>\n\n\n\n

The strongest predictor was a high SCORAD score at age three. SCORAD captures not only the extent and intensity of eczema, but also pruritus and sleep disruption. A persistently high score at this age reflects more than active inflammation, it signals impaired immune regulation and barrier repair during a critical developmental window\u00b3.<\/p>\n\n\n\n

A second predictor was a history of infantile seborrhoeic dermatitis. Although commonly regarded as benign, cradle cap appears to signal early dysregulation in epidermal lipid metabolism\u00b3. From a nutritional perspective, this is highly relevant, as lipid synthesis and barrier formation depend on adequate essential fatty acids, fat-soluble vitamins, and micronutrients involved in keratinocyte differentiation.<\/p>\n\n\n\n

The third marker was weather sensitivity. Children whose eczema flares with changes in temperature or humidity appear to represent a distinct inflammatory phenotype\u00b3. This pattern points towards instability in mast cell signalling and impaired histamine clearance, rather than simple allergen exposure.<\/p>\n\n\n\n

The fourth, and most biologically revealing, marker was low vascular endothelial growth factor (VEGF). While VEGF is typically elevated in inflammatory states, children with persistent eczema showed paradoxically low levels\u00b3. This finding suggests that chronic eczema is not only a condition of excess inflammation, but one of impaired tissue repair and regeneration.<\/p>\n\n\n\n

Together, these markers tell a coherent biological story, one that moves beyond symptom control towards understanding why the skin is failing to stabilise.<\/p>\n\n\n\n

<\/div>\n\n\n\n
\"Identifying<\/figure>\n\n\n\n
<\/div>\n\n\n\n


Why Repair Fails: Nutrient-Dependent Pathways<\/strong><\/h2>\n\n\n\n

VEGF is central to angiogenesis, tissue repair, and maintenance of epidermal integrity. Its identification as a persistence marker is therefore critical, because VEGF signalling is highly nutrient dependent.<\/p>\n\n\n\n

Vitamin D regulates VEGF receptor expression and endothelial function. Multiple systematic reviews and meta-analyses demonstrate that vitamin D supplementation significantly reduces eczema severity in both adult and paediatric populations\u2074\u207b\u2078. Benefits are most consistent in children with deficiency, with doses around 1,600 IU daily showing the greatest effect\u2074,\u2076. Importantly, these improvements extend beyond immune modulation to barrier repair and tissue regeneration.<\/p>\n\n\n\n

Vitamin A plays an equally essential role. Retinoid signalling directly influences keratinocyte differentiation and VEGF synthesis\u2079. However, some individuals carries polymorphisms in the BCO1 gene that reduce conversion of beta-carotene to active retinol by up to 70 percent. In these children, a diet rich in vegetables may still fail to support adequate retinoid signalling, making preformed vitamin A from foods such as liver, egg yolks, and dairy biologically necessary.<\/p>\n\n\n\n

Zinc is required for multiple enzymes involved in tissue remodelling, immune regulation, and VEGF activation. Suboptimal zinc status is frequently observed in children with chronic inflammatory skin disease, particularly where dietary restriction or prolonged inflammation is present.<\/p>\n\n\n\n

In practice, these pathways explain why some children fail to respond fully to otherwise \u201chealthy\u201d diets. The issue is not diet quality alone, but biological accessibility.<\/p>\n\n\n\n


The Gut\u2013Skin Axis and Microbial Resilience<\/strong><\/h2>\n\n\n\n

Persistent eczema is increasingly recognised as a systemic condition rooted in gut barrier integrity and microbiome composition\u2077,\u00b9\u2070. One of the most influential genetic contributors to this axis is the FUT2 gene, which determines secretor status.<\/p>\n\n\n\n

Individuals with a functional FUT2 gene secrete blood group antigens into the gut mucus layer, providing a preferential substrate for beneficial microbes such as Bifidobacterium and Lactobacillus. Non-secretors lack this substrate, resulting in reduced microbial diversity and a more pro-inflammatory intestinal environment.<\/p>\n\n\n\n

This has downstream consequences. Gut microbes ferment dietary fibre into short-chain fatty acids, particularly butyrate, which plays a key role in maintaining gut barrier integrity and regulating T-regulatory immune responses\u2077. Reduced SCFA production is associated with increased intestinal permeability and heightened systemic inflammation, both of which are implicated in atopic disease.<\/p>\n\n\n\n

For children with reduced microbial resilience, nutritional strategies must move beyond generic fibre advice. Targeted prebiotic diversity and carefully selected fermented foods can help support microbial ecosystems that dampen immune over-activation, without resorting to indiscriminate supplementation.<\/p>\n\n\n\n

<\/div>\n\n\n\n
\"\"<\/figure>\n\n\n\n
<\/div>\n\n\n\n


Histamine Handling and the Weather-Reactive Phenotype<\/strong><\/h2>\n\n\n\n

Weather-reactive eczema is often described as environmental sensitivity, but mechanistically it frequently reflects impaired histamine clearance rather than excessive histamine release.<\/p>\n\n\n\n

Histamine is metabolised primarily by diamine oxidase in the gut and histamine N-methyltransferase in tissues. Genetic variation can reduce the activity of these enzymes by 40 to 60 percent. When physiological histamine release is triggered by temperature or humidity changes, children with reduced clearance capacity experience prolonged inflammatory signalling in the skin.<\/p>\n\n\n\n

Both enzymes are nutrient dependent. DAO requires vitamin B6, vitamin C, zinc, and copper, while HNMT relies on adequate methylation capacity supported by B vitamins and methionine intake. When cofactor availability is insufficient, histamine accumulates, amplifying pruritus and barrier disruption.<\/p>\n\n\n\n

Clinically, this explains why some children flare despite avoidance of obvious triggers, and why symptom control alone fails to stabilise the condition.<\/p>\n\n\n\n


Inflammatory Tone Is Modifiable<\/strong><\/h2>\n\n\n\n

Children with persistent eczema often demonstrate elevated pro-inflammatory cytokines, particularly IL-17 and MIP-1\u03b2, reflecting exaggerated Th17 pathway activation\u00b2. While genetic variation in inflammatory genes such as TNF, IL6, and CRP can predispose to higher inflammatory tone, these pathways are highly responsive to dietary modulation.<\/p>\n\n\n\n

Omega-3 fatty acids from oily fish provide EPA and DHA, which compete with arachidonic acid to produce less inflammatory eicosanoids. Clinical trials consistently demonstrate improvements in eczema severity when omega-3 intake is increased and the omega-6 to omega-3 ratio is corrected\u2079.<\/p>\n\n\n\n

Dietary polyphenols such as curcumin and quercetin further modulate inflammation by down-regulating NF-\u03baB signalling, a master regulator of inflammatory gene expression. These effects extend beyond the skin, influencing gut, immune, and vascular function.<\/p>\n\n\n\n

<\/div>\n\n\n\n
\"\"<\/figure>\n\n\n\n
<\/div>\n\n\n\n


From Theory to Clinic: What Changes in Practice<\/strong><\/h2>\n\n\n\n

This emerging evidence has practical implications. It suggests that persistent paediatric eczema is not simply a failure of topical management, but a reflection of constrained biological capacity for repair, regulation, and resilience.<\/p>\n\n\n\n

In my clinical practice, I use nutrigenomic data alongside detailed clinical history to identify children whose eczema is unlikely to resolve spontaneously. By assessing variation in pathways related to skin repair, vitamin metabolism, microbial resilience, and histamine clearance, it becomes possible to stratify risk and personalise nutritional support conservatively and precisely. This approach forms part of my specialist paediatric eczema work.<\/p>\n\n\n\n

Interventions remain food-first and are designed to support, not replace, medical care. The goal is to create the biological conditions that allow the skin barrier to stabilise and immune responses to mature appropriately.<\/p>\n\n\n\n


Conclusion<\/strong><\/h2>\n\n\n\n

For the children who will not simply \u201cgrow out\u201d of eczema, early identification matters. The science now supports a shift from reactive symptom management towards proactive biological support.<\/p>\n\n\n\n

Nutrigenomic-informed nutrition does not offer a cure, nor does it compete with dermatological care. Instead, it provides a framework for understanding why some children fail to respond as expected, and how targeted nutritional support may alter long-term trajectory.<\/p>\n\n\n\n

As our understanding of eczema deepens, the opportunity lies not in doing more of the same, but in recognising which children need something different.<\/p>\n\n\n\n

References <\/strong><\/p>\n\n\n\n

    \n
  1. Davidson W, et al. Report from the National Institute of Allergy and Infectious Diseases workshop on atopic dermatitis and the atopic march. J Allergy Clin Immunol. 2019;143(3):894\u2013913.<\/a><\/li>\n\n\n\n
  2. Tham E, Leung D. Mechanisms by which atopic dermatitis predisposes to food allergy and the atopic march. Allergy Asthma Immunol Res. 2019;11(1):4\u201315.<\/a><\/li>\n\n\n\n
  3. Lauffer F, et al. Predicting persistence of paediatric atopic dermatitis. Allergy. 2020;75(11):2850\u20132861.<\/a><\/li>\n\n\n\n
  4. Kim MJ, et al. Vitamin D status and efficacy of vitamin D supplementation in atopic dermatitis. Nutrients. 2016;8(12):789.<\/a><\/li>\n\n\n\n
  5. Kim G, Bae J. Vitamin D and atopic dermatitis. Nutrition. 2016;32(9):909\u2013915.<\/a><\/li>\n\n\n\n
  6. Hattangdi-Haridas SR, et al. Vitamin D deficiency and supplementation in atopic dermatitis. Nutrients. 2019;11(8):1854.<\/a><\/li>\n\n\n\n
  7. Zhu TH, et al. Epithelial barrier dysfunctions in atopic dermatitis. Br J Dermatol. 2018;179(3):570\u2013581.<\/a><\/li>\n\n\n\n
  8. Novsa RR, Andina. Effectiveness of vitamin D supplementation in atopic dermatitis. J Adv Res Med Health Sci. 2024;10(01):1\u201310.<\/a><\/li>\n\n\n\n
  9. Ryczaj K, et al. Feeding the skin barrier. Clin Transl Allergy. 2025;15(1):e70105.<\/a><\/li>\n\n\n\n
  10. Yang L, Xia JN. Gut\u2013skin axis in atopic dermatitis. Int J Gen Med. 2025;18:123\u2013135.<\/a><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    Au cours de la derni\u00e8re d\u00e9cennie, une image plus pr\u00e9dictive a commenc\u00e9 \u00e0 \u00e9merger, qui ne consid\u00e8re pas l'ecz\u00e9ma persistant comme une \u201cmalchance\u201d, mais comme l'expression visible de contraintes biologiques sous-jacentes. Ces contraintes sont de plus en plus mesurables et, surtout, nombre d'entre elles peuvent \u00eatre modifi\u00e9es par une intervention nutritionnelle cibl\u00e9e et ax\u00e9e sur l'alimentation.<\/p>","protected":false},"author":4,"featured_media":1020,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"categories":[11,17,15],"tags":[],"class_list":["post-1018","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-children-infants","category-eczema","category-skin-health"],"aioseo_notices":[],"aioseo_head":"\n\t\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t