The DNA Health test is designed to optimise well-being and health by personalising lifestyle and diet choices and, where necessary, using supplements tailored to offset any particular nutritional deficit based on specific gene variants.

The DNA Health approach assists the healthcare practitioner in establishing the optimal nutrition necessary for good health, longevity and disease risk mitigation. Diet is a key factor in determining genomic stability as it impacts on all relevant pathways:  exposure to dietary carcinogens, biotransformation, DNA repair and synthesis, and apoptosis. Current recommended dietary allowances for vitamins and minerals are based largely on the prevention of diseases of deficiency. However, because diseases of lifestyle are partly caused by damage to DNA it stands to reason that we should focus our attention on defining optimal requirements of key minerals and vitamins for preventing genomic instability.

Additional attention should be paid to individuals with genetic polymorphisms that alter the bioavailability of specific micro-nutrients and the affinity of specific key enzymes for their micro-nutrient co-factor.

Clinical Value

• Highlights specific metabolic pathways that may require extra support
• Provides recommendations that involve optimisation of quantities of certain nutrients, vitamins and minerals
• Suggests whether an individual is better able to reduce their cholesterol levels through diet, as opposed to through medication
• Provides an indication of the degree of susceptibility to the harmful effects of carcinogens ingested in the diet

The DNA Health Test Report provides: 

• The level of impact of any genetic variants identified
• An explanation of their impact on health
• Appropriate nutritional and lifestyle recommendations

The results are divided in sections of key metabolic function, so that genetic weaknesses and strengths within a functional area can be easily identified. 

Overview

Tests for:

Gene variations associated with metabolic and biological processes

Analytes measured:

Lipid Metabolism

LPL:  Removes lipids from the circulation by hydrolysing triglycerides into free fatty acids.
CETP:  Plays a key role in the metabolism of HDL and mediates the exchange of lipids between lipoproteins.
APOC3:  Plays an important role in cholesterol metabolism.
APOE:  Is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. Affects antioxidant requirement.

B Vitamins/Methylation

MTHFR:  Directs folate from the diet either to DNA synthesis or homocysteine re-methylation.
MTR:  Catalyses the re-methylation of homocysteine to methionine.
COMT:  Catalyses the transfer of a methyl group from S-adenosylmethionine to catecholamines, including the neurotransmitters dopamine, epinephrine, and norepinephrine.
MTRR:  Catalyses methylcobalamin, which is essential for maintaining adequate intracellular pools of methionine. It is also responsible for maintaining homocysteine concentrations at non-toxic levels.
CBS:  Catalyses the conversion of homocysteine to cystathionine and is directly involved in the removal of homocysteine from the methionine cycle.

Detoxification

CYP1A1:  The cytochrome P450 enzyme converts environmental pro-carcinogens to reactive intermediates, which are carcinogenic.
GSTM1:  Influences Phase II detoxification. It is responsible for the removal of xenobiotics, carcinogens, and products of oxidative stress.
GSTP1:  Influences the metabolism of many carcinogenic compounds.
GSTT1:  A member of a super family of proteins that catalyses the conjugation of reduced glutathione.
NQO1:  Quinone Reductase is primarily involved in the detoxification of potentially mutagenic and carcinogenic quinones derived from tobacco smoke, diet and oestrogen metabolism.

Inflammation

IL-6:  Plays a crucial role in inflammation by regulating the expression of C reactive protein (CRP).
TNF-A:  TNFa is a pro-inflammatory cytokine, secreted by both macrophages and adipocytes, which has been shown to alter whole body glucose homeostasis, and has been implicated in the development of obesity, obesity-related insulin resistance and dyslipidemia.

Food Responsiveness and Sensitivity

MCM6:  Associated with adult hypolactasia.
FADS1:  Influences blood fat concentrations by affecting desaturase enzyme efficiency.
CYP1A2:  This detoxification enzyme influences the ability to metabolise caffeine.
ACE & AGT:  Part of the renin-angiotensin system and response to salt.
HLA DQ2/DQ8: Major genetic predisposition for coeliac disease

Vitamin Metabolism

BC01:  Catalysing carotenoids to retinal (vitamin A)
CYP2R1: Conversion of vitamin D to 25(OH)D
FUT2: Vitamin B12 absorption and transport
GSTT1: Contributing to glutathione-ascorbic acid (vitamin C) antioxidant cycle


Iron Overload

HFE:  Regulates iron absorption by regulating the interaction of the transferring receptor with transferrin. Hereditary haemochromatosis results from defects in the HFE gene.

Oxidative Stress

eNOS:  Influences vascular tone and peripheral vascular resistance. It also has vaso-protective effects by suppressing platelet aggregation, leukocyte adhesion and smooth muscle cell proliferation.
MnSOD/SOD2:  Has vital anti-oxidant activity within the cell, especially within the mitochondria.  It destroys the radicals that are normally produced within cells.

Bone Health

VDR:  Has a profound influence on bone density.
COL1A1:  Influences the ratio of collagen-alpha chains produced by bone cells, affecting bone mineralisation of bone and bone strength.

Insulin Sensitivity

PPARG:  Involved in adipocyte differentiation. It is a transcription factor activated by fatty acids, and is also involved in the regulation of glucose and lipid metabolism.
TCF7L2:  Influences blood glucose homeostasis – both  insulin secretion and resistance.
FTO:  Influences susceptibility to obesity and risk for type 2 diabetes.
SLC2A2:  Facilitates glucose induced insulin secretion and is involved in food intake and regulation.

Practical

Test type:
DNA: Gene, health, nutritional genomics, lifestyle

Sample required:
Bloodspot

Privacy policy:
The DNA and the original sample material are destroyed after 3 months, so that there are no names or other identifiers on the samples. The samples are analysed only for the SNPs that are included in the tests at DNALife, and no other research or analyses are performed without a separate permission from the patient. We do not give or sell the results to any third parties.