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Protein-energy malnutrition

Protein-energy malnutrition (PEM), or also known as protein-calorie malnutrition is a malnutrition and deficiency syndrome in organisms, especially humans caused by the inadequate intake of macronutrients through food in their diet. more...

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It is characterized not only by an energy deficit due to a reduction in all macronutrients but also by a deficit in many micronutrients. Cells in an organism require these sources of nutrients to perform cellular respiration in order to produce adenosine triphosphate, which is the energy currency of most cellular functions.

When energy or carbohydrate intake is lacking, the organism's body must break down its own proteins which form the major building components of the cells in the organism in order to continue to provide energy for itself. This syndrome is one example of the various levels of inadequate protein or energy intake between starvation and adequate nourishment. Although infants and children of some developing nations dramatically exemplify this type of malnutrition, it can occur in persons of any age in any country.

Classification and etiology

Clinically, protein-energy malnutrition has three forms: dry (thin, desiccated), wet (edematous, swollen), and a combined form between the two extremes. The form depends on the balance of protein or nonprotein sources of energy, such as carbohydrates or milk respectively. Each of the three forms can be graded as mild, moderate, or severe. Grade is determined by calculating weight as a percentage of expected weight for length using international standards (normal, 90 to 110%; mild protein-energy malnutrition, 85 to 90%; moderate, 75 to 85%; severe, < 75%).

The dry form, marasmus, results from near starvation with deficiency of protein and nonprotein nutrients. The marasmic child consumes very little food often because his mother is unable to breastfeed and is very thin from loss of muscle and body fat.

The wet form is called kwashiorkor, an African word literally meaning first child-second child. It refers to the observation that the first child develops protein-energy malnutrition when the second child is born and replaces the first child at the breast of the mother. The weaned child is fed a thin gruel of poor nutritional quality (compared with breastmilk) and fails to thrive. The protein deficiency is usually more marked than the energy deficiency, and edema results. Children with kwashiorkor tend to be older than those with marasmus and tend to develop the disease after they are weaned.

The combined form of protein-energy malnutrition is called marasmic kwashiorkor. Children with this form have some edema and more body fat than those with marasmus.

Epidemiology

Marasmus is the predominant form of protein-energy malnutrition in most developing countries. It is associated with the early abandonment or failure of breastfeeding and with consequent infections, most notably those causing infantile gastroenteritis. These infections result from improper hygiene and inadequate knowledge of infant rearing that are prevalent in the rapidly growing slums of developing countries.

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Assessing protein energy malnutrition
From Alcohol Health & Research World, 1/1/92

Because the biological response to deprivations of calories and proteins is multifaceted, a variety of techniques and laboratory tests can be used to assess protein energy malnutrition (PEM). Many of the tests, including those described below, are more familiar to dieticians than to clinicians (Blackburn et al. 1977; Antonow and McClain 1985; Figure 1).

Tests of Body Weight

A person's ideal body weight is based on height and can be determined from the Metropolitan Standards table, which is reproduced in any textbook of nutrition. Because of the ease with which height and weight data can be obtained, a person's percentage of the ideal body weight is commonly used as an assessment of PEM. However, caution must be exercised. For example, in the case of an alcoholic with liver disease, fluid retention is common and can mask the severity of weight loss. The total water in the body can be measured by the technique known as isotope dilution; however, this typically is not done. More often, clinicians obtain less reliable estimates of body water by weighing the patient before and after excessive excretion (diuresis).

Anthropometric Tests

Anthropometry is the science of measuring the human body and its parts. Two common anthropometric measurements are skinfold thickness and midarm muscle circumference and area. Skinfold measurements are estimates of stores of body fat. These measurements can be made in a variety of locations throughout the body, but clinicians usually measure the triceps. Researchers have reported significant correlations between skinfold measurements and morbidity and mortality of patients with alcoholic liver disease (Mendenhall et al. 1986). Midarm muscle circumference and area is an indirect estimate of skeletal muscle mass based on the circumference of the midarm and skinfold thickness of the triceps.

Creatinine Height Index

The creatinine height index is another method for estimating muscle mass. This index is based on the amount of creatinine in urine during a 24-hour period. Healthy muscle produces creatinine at a relatively constant rate in proportion to muscle mass. Decreases in muscle mass lead to proportional decreases in the level of creatinine in urine. Factors affecting excretion of creatinine include large amounts of meat in the diet, altered renal function, and drugs, such as steroids, that alter muscle metabolism.

Visceral Proteins

The concentrations of nonmuscle proteins known as visceral proteins also decrease during the course of PEM and therefore can be used to diagnose and monitor malnutrition. Those most commonly measured are the transport proteins circulating in the bloodstream, including albumin, transferrin, prealbumin, and retinol-binding protein. Studies have revealed that diets deficient in protein result in decreases in the rate of synthesis of albumin, but with a concomitant and perhaps compensatory reduction in the rate of degradation of albumin (Rothschild et al. 1969). The observed reduction in concentration of serum albumin develops slowly and has a long recovery time. This finding has led many to conclude that such visceral proteins are more sensitive and responsive to the changes associated with PEM and, hence, are preferred "tools" for monitoring nutrition.

However, changes in concentrations of some proteins can reflect abnormalities that are independent of malnutrition, for example, deficiencies in zinc, iron, and vitamin A. Also, infections, thyroid dysfunction, liver disease, and renal disease can alter visceral protein synthesis and degradation independently of malnutrition. In the case of alcoholic liver disease, the reduction in visceral proteins may be as much a reflection of the liver's inability to synthesize proteins as a result of the shortages in amino acids associated with malnutrition. Despite the lack of specificity, tests of visceral proteins are used widely as indicators of nutritional status and correlate well with morbidity and mortality (Buzby et al. 1980; Mendenhall et al. 1986).

COPYRIGHT 1992 U.S. Government Printing Office
COPYRIGHT 2004 Gale Group

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