Nutritional assessment and therapies

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Chapter 2 Nutritional assessment and therapies

With contribution from Dr Antigone Kouris-Blazos

Introduction

The importance of nutrition in general medical practice has paralleled the increasing prevalence of lifestyle related disorders such as obesity, diabetes, and heart disease. In fact, alongside dermatology and psychological disorders, nutritional disorders are among the most common problems encountered by doctors and there is pressure for the general practitioner to provide competent nutritional assessment, diagnosis and therapy.1 It has been estimated that over 70% of patients seen in general practice are at high risk of having or developing a nutritional deficiency and many patients will exhibit symptoms suggestive of nutritional inadequacy or imbalance which is contributing to their illness.2, 3

The Australian National Health Survey in 2004–5 reported that 86% of Australians between 18–64 years do not consume the recommended 5 serves of vegetables each day and 46% do not consume the recommended 2 serves of fruit each day.4 In 2008 rising petrol and food prices (especially for fresh produce but not for processed/take away foods) were reported to potentially affect shopping trends with less fresh produce being purchased.5 Furthermore, the costs of healthy foods such as bread and milk is rising far greater than the cost of nutrient poor energy dense foods (such as cakes, soft drinks and biscuits), which will impact on food choices and the diet in lower socioeconomic groups.6

This may be further compounded by emerging evidence from the UK and US (Australian data lacking) that there has been declining levels of minerals in our fruit and vegetables over the last 50 years, especially for magnesium dropping by about 45% (see page 23 ‘Dietary history and assessing food and nutrient intake’). Markovic and Natoli report paradoxical nutrient deficiencies such as zinc, iron, vitamin C and D and folate in the obese and overweight due to eating high-energy foods that are also high in saturated fats, salt and sugar, with poor nutrient content.7 The authors note that this condition is under-recognised and therefore not treated. The Public Health Association of Australia released a report in 2009 ‘A Future for our Food: addressing public health, sustainability and equity from paddock to plate’ outlining the urgent need for Australian food policy to encourage food choices that are environmentally sustainable and address the re-emergence of nutrient-deficiency related diseases.8

The Australian dietary guidelines and core food groups are currently undergoing revision. The Public Health Association of Australia would like to see the new guidelines address the re-emergence of nutrient-deficiency related disease and food sustainability. Specific recommendations include: reduced total intake of animal products; reduced reliance on ruminant meat; promotion of sustainable proteins, especially legumes, nuts, eggs and chicken; promotion of seasonal fruit and vegetables, legumes and grains that are grown using production methods appropriate to the region. The report highlights that shifting less than 1 day per week’s worth of calories from red meat and dairy products to chicken, fish, eggs, or legume-based diet achieves more green house gas reduction than buying all locally sourced food. In addition, consuming less meat and more plant-based foods may be 1 type of measure that will lead to increased sustainability and reduced environmental costs of food production systems.8

The Australian National Children’s Nutrition and Physical Activity Survey also highlights the growing epidemic of obesity in children — estimated at 17% of children considered overweight and 6% obese in Australia — with poor quality diets with significant nutritional shortfalls, particularly vitamin D, E, iodine and iron.9

Suboptimal intake of vitamins from diet is common in the general population, particularly children and the elderly, and a risk factor for chronic diseases such as cardiovascular disease, neural tube defects, colon and breast cancer, osteopenia and fractures.10

Other risk groups identified include vegans, drug and alcohol-dependent individuals, hospitalised patients and patients with malabsorption.

If these trends continue nutritional deficiencies may become more commonplace in the community. Doctors, dietitians, nurses and other allied health professionals may need to become more active and skilled at detecting signs and symptoms of nutritional deficiencies/insufficiencies. Improving the nutritional status of patients will help improve clinical outcomes/wellness and reduce morbidity and mortality and is thus of increasing importance to comprehensive medical care. In order to determine whether a patient’s nutritional status needs improving, a nutritional assessment is required.

Nutritional assessment will identify the high-risk patient (see Table 2.1) for nutrient inadequacies or excesses which in turn will contribute to a nutritional diagnosis. Once the diagnosis is made it is then possible to put in place the nutritional therapy of the patient.

Table 2.1 Identifying patients at high risk of nutrient deficiency or insufficiency

(Source: adapted from Wahlqvist M, Kouris-Blazos A. Nutrition — is diet enough? J Comp Med 2002: 46)11

Nutritional assessment is based on information gathered from:

Table 2.2 Presentations and signs (can include) to consider with specific vitamin deficiencies (rare or sub-clinical deficiency in Western populations)

Micronutrient Signs
Vitamin A
Vitamin B1
Vitamin B2
Vitamin B3
Vitamin B6
Vitamin B12
Vitamin B complex/folate
Vitamin C
Vitamin D
Calcium (Ca) and/or magnesium (Mg) Positive Chvostek sign
Iron (Fe) Koilonychia, leucoplakia, Plummer–Vinson syndrome
Zinc (Zn) Acne, stretch marks, white spots on nail
Iodine (I) Weight gain

Medical history

The medical history may reveal a disease that interferes with the patient’s ability to eat (e.g. Cerebrovascular accident and Parkinson’s disease) or the body’s use of nutrients (increased excretion of magnesium and chromium in diabetes or reduced absorption of several nutrients in Crohn’s disease). The genetic predisposition may also provide clues e.g. reported weight loss or diarrhoea could be due to coeliac disease which runs in the family.

Signs and symptoms of nutritional deficiencies

Clinical symptoms and anthropometric measurements will provide further clues to the nutritional puzzle. However, symptoms (manifestations reported by the patient) and signs (observations made by a clinician) can occur late in the development of the nutritional problem. Thus diagnosis of a nutritional deficiency cannot usually be made solely on the basis of a clinical examination. This is mainly because many nutrition-related signs and symptoms are non-specific and can occur for non-nutritional reasons. Usually the presence of a group of related clinical signs and symptoms is a better indication than a single sign or symptom.12 For example, the finding of follicular hyperkeratosis isolated to the back of a patient’s arms is a fairly common, normal finding. On the other hand if it is widespread on a person who consumes little fruit and vegetables and smokes regularly (increasing vitamin C requirements) vitamin C deficiency is a possible cause. Not surprisingly, the tissues with the fastest turnover rates are the most likely to show signs of nutrient deficiencies or excesses e.g. hair, skin and lingual papillae (an indirect reflection of the status of the villae of the gut)13 (see Tables 2.2 and 2.3 for clinical signs and symptoms of possible nutritional deficiencies).

A thorough medical and nutritional history, together with a thorough physical examination is necessary to detect nutrient deficiencies (occasionally this may be subtle i.e. nutritional insufficiency). When taking a nutritional history, if limited by time, ask patients to recall what they ate and drank in the last 24–48 hours and/or ask them to bring a 1-week food diary at their next consultation. If time permits, then a more extensive dietary assessment would be helpful as discussed under Dietary history and assessing food and nutrient intake in this chapter. Examples of symptoms suggestive of nutrient deficiencies include gum bleeding (vitamin C), numbness of feet (folic acid and B1 deficiency), night blindness (vitamin A), poor immunity and recurrent infections (vitamins A, C, D and zinc), poor appetite (B group vitamins and zinc), muscle cramps (calcium, magnesium), tremor (magnesium), poor memory (B group vitamins, folic acid and various minerals e.g. magnesium), loss of libido (B group vitamins, folic acid), tiredness (any nutrient), mood disorders (B group vitamins, vitamin C and zinc), poor wound healing (protein, zinc, vitamin C), sore tongue (several B group vitamins) and loss of taste (zinc). Physical examination of the patient may identify a number of signs suggestive of nutrient deficiency (see Tables 2.2 and 2.3).

Table 2.3 Clinical symptoms and signs of nutrient deficiencies/insufficiencies

Clinical symptoms and signs Consider low intake/deficiency (may warrant blood/urine/faeces testing)
HEAD
appetite poor Zni, v, Mgiii, Feiii, B1vi, B3vi, folatevi, excess vit Ai
nausea (esp with fatty foods) B3vi
fatigue/tiredness/irritable B6vi, B12vi, folatevi, Zni, v, vi, vit Cvi, Feiii, vi, chromium (Cr)vi, thyroid, excess vit Av, proteinvi
sugar cravings/hyperglycaemia insulin resistance, Mg, Criii, v, vi, Zn, vit E
moody/depressed proteinvi, B1vi, B3iii, B6iii, vi, B12vi, vit Cvi, Mgvi, Zniii, iodine, thyroid, vit D
anxiety/agitation Crvi, Mgvi, vit Dvi
migraine B2vi, coenzyme Q10 (CoQ10)
headache B3iii, B12vi, folatevi, Feiii, Mg if cervicocranial, excess vit Ai, iii
sleep disturbance B6vi, Mgvi, vit Cvi
sleep onset delay vit Dvi
poor dream recall B6vi
insomnia/restless sleep vit Dvi, Cavi, B3iii
non-refreshing sleep Mgvi
night sweats-back of head/scalp vit Dvi
low libido Fe (women) iii, Zn (men), low testosterone, thyroid
impaired memory/cognition/dementia B1iv, vi, B12iii, iv, vi, B3iii, iv, v, folateiv, vi, Fevi, Znvi, iodine
HAIR/SCALP
hair thinning/loss/alopecia proteiniv, B2vi, EFAvi, Zniii, vi, Fevi, Biotini, iii, v, vi, excess vit Aiii, excess selenium (Seiii) thyroidi, iodine
dry dull hair essential fatty acid (EFA)vi, vit Avi
easily plucked hair proteiniv
dry coarse/brittle hair proteiniv, biotiniv, Fevi, Zni, vi, Iodine, hypothyroid, EFAvi, excess vit Ai, iii
depigmentation/dyschromotrichia copper (Cu)i, Sei
hair growth arrest Zni
diaphoresis of scalp (night) vit Dvi
dry flaking hair and scalp vit A, Zn, Se
dandruff Znvi, Mgvi, biotinvi, Se
prematurely graying hair Cuvi, Biotinvi, vit B12iii, vi
coiled/cork screw hairs vit Ciii (hair shaft flat instead of round in cross section)
EYES
tearing/burning/itching vit B2v
dark/crimson under eye circles Fe, allergyvi, liver problems

vit Ai, vi, Zni, Biotiniii (conjunctivitis) pale conjunctiva Feiii muddy sclera vit Cvi yellow sclera liver functioni, vi photosensitivity vit B2iii, vi, Zniii bitot spots/white thick patches vit Ai, Zni impaired night vision vit Aiii, vi, Zniii long sightedness vit Dvi impaired visual acuity/blurred EFAvi, xs vit Ai pterygium (thickness) vit Cvi, B3vi, EFAvi twitching eye/spasms facial muscles Mgi, iii, vi, Cai, iii, Ki macular/retinal degeneration age, lutein, zeaxanthin, excess blood sugar NOSE scaling/red folds nasolabial seborrhea vit B2iii, vi (red greasy folds), B6iii, omega-6iii (dry folds) poor smell/anosmia Znv, vi, vit Av EARS noise intolerance Mgvi post aural flush Znvi, EFAvi tinnitus Feiii TONGUE/MOUTH

vit B3i, iii, iv, v, B12i, iii, iv, v, folatei, iv, v, Fei, iv, v, vi bright red smooth/glossitis vit B2i, iv, B6i, iii, iv, v, B12i, iv, folatei, iv, v, Fei, iv, v, vi, biotini, v large beefy tongue hypothyroidi, iodinei magenta/blue tongue vit B2i, iii, v, Biotini white/pale smooth Fei yellow/brown tongue bowel dysfunction/dysbiosisvi, low HCLvi berry like red tongue vit B complexi fissured/creviced tongue vit B3iv, v scalloped tongue Mgvi, vit B3vi strawberry tip/cherry tip tongue vit B3vi, B6vi burning sensation of mouth/throat Dvi lips cheilosis (burning/soreness) vit B2iii, iv, v, B3iii, iv, B6iv, v angular stomatitis vit B1i, B2i, iii, iv, v, B3i, iii, iv, B6iii, iv, folatev, B12i, v, Fei halitosis vit B3vi, low HCL, dysbiotic bacteria, hypothyroid; liver problems periodontal disease/loose teeth vit Cvi, CoQ10vi, Cavi bleeding gums/gingivitis vit Ci, iii, iv, B2iv, vitKvi, xs vit A (red gingiva around teeth)i, iii gum recession proteinvi, CoQ10vi mouth ulcers vit B12vi, vit Avi, folatevi crimson crescents back of mouth food sensitiviesvi intense thirst xs vit Dvi, B1/wet beri beriiii impaired taste Zni, v, vit Aiii loss of tooth enamel Caiv HANDS/NAILS finger pulp atrophy proteinvi cold hands Feiii, Mgvi, vit Evi, EFAvi, thyroid vertical corrugations — pronounced (beaded nails) vit Bii, proteinvi, Znvi, diabetesii, thyroidii, Addisonsii vertical corrugations — unpronounced Agei, RAi, PVDi, Lichen planusi pronounced central ridge Fei, folatei, proteini horizontal grooves/Beau’s lines proteinvi, past severe illness/surgeryii, MIii, Zni, Sei, Caii leukonychia (white spots) Znvi half moons base of nails vit B6vi dry thin brittle nails proteinvi, malnutritionii EFAvi, Fevi, Ca/osteopeniaii, thyroidii peeling/splitting nails Cavi proteinvi spoon shaped/brittle nails Fei, iii, vi, low cysteine/methioninei, diabetesi soft/papery/bitten nails Znvi, proteinvi growth arrest/thickened nails proteinvi, Zni yellow nails vit Evi black/red thickened nails xs Sei egg shell nails vit Avi clubbed nails lung problemsii, IBDii, coeliacii, hyperthyroidii brown nail beds or skin creases vit B12iii white nail beds Seiii paronychia excess Seiii, Zniii MUSCLE generalised muscle pain/ache tender muscles
B1iv, vit Ev, Cai, v, Mgi, vi, potasium (K)i, v, Sei, iii, vit Dv, vi, coma, iodine
cramps Caiii, v, Mgvi, vit B5vi, Feiii, K, Na, vit Ciii, vit Dvi muscle twitching/spasms (hyper-reflexia) B6v, Mgi, iii, v, vi, Cai, iii, Ki, vit Dvi muscle atrophy face, hands, chest, loss of tissue recoil back of hand proteinvi, B1vi calf/muscle tenderness vit Ev (intermittent claudication), B complexiv, vi muscle weakness/wasting (difficulty up/down stairs)iii proteiniv, vit Dv, Kv, Ca, thiamin decreased muscle reflexes B complexvi, vit Evi SKIN excessive ageing of skin/wrinkles vit Evi perifollicular hyperkeratosis (toad skin) commonly seen on upper arms/thighs vit Ai, iv, vi, Zni, B complexiii, vit Ciii, v, EFAiii perifollicular petechiae/haemorrhages vit Ci, iii, v, vit Ki, iii (causes petechiae unrelated to hair; sometimes seen with prolonged antibiotic treatment) shark skin/dyssebacea (sebum plugs in follicles/face/body) vit B2iii vit B2iii, v(nasolabial/scrotum), vit B3iii, vit B6i, iii, v, Biotinvi, Cui, EFAvi dry scaly/coarse dermatitis Zniii, v, Iodinei, vit B3iii, omega-6i, iii, omega-3vi, vit Cv, vit E, biotini, v, vitAv, vit A excessi, iii, v dry ‘fish scale’, ‘flaky paint’ vit Aiv, Zniv, v especially on the legs hyperpigmentation non scaly macules/patches insulin resistancevi, vit A, Zniii, v, vit C, vit B12iii, vit B6vi, folateiii, EFA, evening primrose oil (EPO), vit B3iv (see also dermatitis) hyperpigmented scaly dermal patches on face/limbs (pellagra) vit B1, vit B3i, biotini, v, Zniii, v, EFA unusual skin rash vit B6 or excess supplement use spider veins vit Cvi liver spots (ceroid accumulation) vit Evi eczema biotinvi, Zniii, omega-3vi, omega-6/EPOi, iii, gluteni rosacea vit B2, hypochlorhydria/gastric dysfunctionvi, dysbiotic bacteria/H pylori infectionvi psoriasis vit Dvi, EFAvi, vit Aiv, Zniii acne EFAvi, Znvi, vit Avi, vit Ciii, dysbiotic bacteria, bowel dysbiosisvi, high GI diet/insulin resistancevi stretchmarks Znvi, vit Evi, Bvivi wound healing/lesions on pressure areas vit A, B6vi, vit Cv, vi, Zni, iii, v, EFAvi, proteinvi, biotinvi easy bruising vit Kiv, vi, dysbiotic bacteriavi, protein, vit Civ, vi, blood thinning medication blood mottling arms/legs vit B6vi itchy skin/rashes liver problems NERVES/PAIN/BONES impaired coordination/balance, disorientation/ataxic gait vit B1i, vi, B12iii, v (neurological changes can occur without haematologic changes), B3iv, vit Eiv, vi neuropathy (weakness, ataxia, pins/needles, parasthesia, foot/wrist drop, reduced tendon reflexes, numbness of fingers/feet/lips/tongue fine tactile sense, vibratory sense, position sense) vit B1i, iv, vi, B2iii, vi, B6iii, iv, B12iv, v, carnitine, EPO, vit B6 toxicityiii, folateiii, Mgi, Cai, Ki, omega-3iii, Criii, v Fevi, vit Eiv, v, lipoic acid neuralgia/paralysis/paresthesia vit B1iv, B3iii, B12iii, iv, v Mgiv, v tetany Caiv, v, Mgiv, Kv diminished reflexes Iodineiv postural hypotension vit B6/B complexvi, Fevi (general hypotension) bone/joint pain vit Civ, v, vi, xs vit Aiv, v, vit Div, v, Cav, omega-3vi, Znvi, Boronvi low bone density excess vit Av Cav, Mgv, vit Dv, Cav, Zn, vit K DIGESTION constipation/bloating Feiii, B3vi, low HCL/enzymes, gluten, food intolerances, dysbiosis, candida management, vit D excess diarrhoea Feiii, excess Mg/vit Ci, Zni, B3iii, vi, B12iii folatev, biotinv, fructose, fructans belching/flatulence/reflux vit B12iii, low hydrochloric acid (HCL), H Pylori, allergen, lactose, fructose poor digestion vit B3vi, low stomach acid (HCI)vi MENSTRUAL delayed/<flow periods/irregular oligomenorrhoea/sub-fertility Feiii, vit Evi, EFAsvi, insulin resistancevi, Znvi mastalgia vit Evi, vit Avi, omega-3vi/EFA imbalancevi PMS vit B6vi, Cavi, Mgvi, EFAvi dysmennorrhoea/menorrhagea Cavi LEGS/FEET heels — hyperkeratosis/dry/cracked vit Evi, EFAvi soles — hyperkeratosis vit Avi cold feet/<peripheral perfusion vit Evi, EFAvi, Mgvi, vit B6, thyroid (vit A, Zn, I, Fe) burning paresthesias in feet vit B5iii, B1iii arch collapse proteinvi calf muscle tenderness vit Evi, B1iii oedema K, Mg, vit B1i, iii, Feiii, proteiniv, quercetin GROWTH poor Fei, Zni, vi, Iodinei, iii, proteini, energyi, vit Di, Ca, omega-6iii, vitAv IMMUNITY/INFECTIONS/CANCER immuno-dysfunction Zniii Sevi, vit Cvi, vit Evi, vit D

Important note: The list in Table 2.3 is not definitive and is based on combined clinical experience and scientific evidence. Assessment and treatment should be based on your own clinical judgment (i.e. dietary history and physical examination) and confirmed with pathology testing. Symptoms may also occur from other non-nutritional related diseases.

i McLaren DS. A Colour Atlas and Text of Diet-Related Disorders. 2nd edn. London England: Wolfe & Mosby — Year book Europe Ltd, 1992.

ii Medscape. Examining the Fingernails When Evaluating Presenting Symptoms in Elderly Patients. Online. Available: www.medscape.com (accessed 7 Aug 2008).

iii McLaren DS. Clinical manifestations of human vitamin and mineral disorders: a resume. In: Shils M, Olson JA, Shike M, Ross C. Modern Nutrition in Health and Disease. 9th edn. Williams & Wilkins, 1999;485–503.

iv Newton MJ, Halsted CH. Clinical and functional assessment of adults. In: Shils M, Olson JA, Shike M, Ross C. Modern Nutrition in Health and Disease. 9th edn. Williams & Wilkins, 1999;895–902.

v Heimburger DC, Ard JD. Handbook of Clinical Nutrition. 4th edn. Mosby Elsevier 2006.

vi Sydney-Smith M. Nutritional Assessment. J Comp Medicine 2006; Jan-Feb 28–40; and Nutritional Assessment Workshop Seminar slides, March 2008.

Anthropometry

Anthropometry is a measurement and study of the human body and its parts and capacities and can provide information on body muscle mass, fat reserves and fat distribution. Unintentional weight loss during illness often reflects loss of lean body mass, especially if rapid and not caused by diuresis. Body mass index (BMI) alone is not ideal in determining health risk because it does not reflect the amount of muscle or distribution of fat mass. The waist circumference is a good indicator of abdominal obesity but it does not differentiate between visceral/internal fat (the one linked to chronic diseases) and the more inert subcutaneous abdominal fat. Convenient and inexpensive electrical impedance devices are increasingly being used by clinicians to determine muscle mass, fat mass, visceral fat and body water. When assessing health risks associated with a patient’s weight, it may be useful to remember that higher weight in the elderly has been associated with lower mortality risk — staying in the ‘normal’ BMI range during young adulthood is recommended but slowly gaining weight during the elderly years does not seem to pose a health risk. On the other hand, obesity during young adulthood and being underweight during the elderly years leads to higher mortality rates.14 Furthermore, if a patient does a lot of exercise but is still overweight this poses a lower mortality risk than being slim and unfit.15 There is also emerging evidence of a subgroup of healthy obese that could be genetically determined or could relate to the dietary pathway in becoming overweight. For example, becoming overweight on a Mediterranean diet may not pose the same health risk as becoming overweight on a Western diet. This possibility has been identified in elderly Greek migrants in Australia that despite being overweight had lower mortality rates than their leaner Anglo-Celtic counterparts.16

Socioeconomic/lifestyle circumstances

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