Background In developing countries the duration and severityof diarrheal illnesses are greatest among infants and youngchildren with malnutrition and impaired immune status, bothfactors that may be associated with zinc deficiency. In childrenwith severe zinc deficiency, diarrhea is common and respondsquickly to zinc supplementation.
Methods To evaluate the effects of daily supplementation with20 mg of elemental zinc on the duration and severity of acutediarrhea, we conducted a double-blind, randomized, controlledtrial involving 937 children, 6 to 35 months of age, in NewDelhi, India. All the children also received oral rehydrationtherapy and vitamin supplements.
Results Among the children who received zinc supplementation,there was a 23 percent reduction (95 percent confidence interval,12 percent to 32 percent) in the risk of continued diarrhea.Estimates of the likelihood of recovery according to the dayof zinc supplementation revealed a reduction of 7 percent (95percent confidence interval, -9 percent to +22 percent) in therisk of continued diarrhea during days 1 through 3 and a reductionof 38 percent (95 percent confidence interval, 27 percent to48 percent) after day 3. When zinc supplementation was initiatedwithin three days of the onset of diarrhea, there was a 39 percentreduction (95 percent confidence interval, 7 percent to 61 percent)in the proportion of episodes lasting more than seven days.In the zinc-supplementation group there was a decrease of 39percent (95 percent confidence interval, 6 percent to 70 percent)in the mean number of watery stools per day (P = 0.02) and adecrease of 21 percent (95 percent confidence interval, 10 percentto 31 percent) in the number of days with watery diarrhea. Thereductions in the duration and severity of diarrhea were greaterin children with stunted growth than in those with normal growth.
Conclusions For infants and young children with acute diarrhea,zinc supplementation results in clinically important reductionsin the duration and severity of diarrhea.
Among children in developing countries, diarrheal illnesses,especially those of prolonged duration, are important causesof growth retardation and death.1,2,3,4,5 Episodes of diarrhea,which usually resolve within a few days in a healthy child,persist longer in children with malnutrition,6,7 impaired cellularimmunity,7,8,9 or recurrent diarrhea.10
We hypothesized that zinc deficiency is a link between theserisk factors and the duration of diarrhea. Diarrhea is consistentlyfound in children with severe zinc deficiency,11,12 as wellas in animals with zinc depletion13; it responds quickly tozinc supplementation.14 Zinc deficiency can result in growthretardation, especially stunting,15 and impairment of immunefunction.16,17 Finally, diarrhea leads to excess zinc lossesand could contribute to zinc deficiency,18,19,20,21 especiallyif the zinc content of the diet is limited.22,23 To evaluatethis hypothesis, we investigated the effect of zinc supplementationon the duration and severity of diarrhea in a community-based,double-blind, controlled trial.
Methods
The trial was conducted in the Kalkaji neighborhood of New Delhi,India, an urban population of low socioeconomic status, betweenSeptember 1992 and November 1994. The incidence of diarrheain this population is nine episodes per year for children upto 11 months of age and five episodes per year for children12 to 36 months of age.24
Screening and Selection of Patients
All patients with diarrhea who presented to the dispensary atKalkaji, where a special diarrhea clinic was operated by researchphysicians, were screened for enrollment in the trial. Children6 to 35 months of age who were reported to have passed at leastfour unformed stools in the previous 24 hours, who had had diarrheafor less than seven days, and who were permanent residents ofKalkaji were selected for inclusion. Children who presentedto the clinic a second time, those who were judged by the physicianto have malnutrition requiring hospitalization, and those whoseparents did not provide consent were excluded. The parents ofchildren without dehydration or with mild dehydration were advisedto give them 50 ml of oral rehydration solution per kilogramof body weight at home and were given packets of oral rehydrationsalts. Parents were advised to continue feeding the child hisor her usual diet. Children who presented with dehydration ofmore than 7 percent as assessed clinically were enrolled, supplementationwas started, and the children were referred to the All IndiaInstitute of Medical Sciences for rehydration.
The study was approved by the human research review committeesat the All India Institute of Medical Sciences, Johns HopkinsSchool of Hygiene and Public Health, and the World Health Organization(WHO). The consent form was read to a parent, and written informedconsent was obtained for each child's enrollment.
Base-Line Assessment
A base-line assessment, including a detailed physical examination,was performed by a research physician at the time of enrollment.Weight was measured using an electronic scale with a sensitivityof ±10 g (SECA, Columbia, Md.) by two independent observers;length (for children less than 24 months old) or height (forchildren 24 to 35 months old) was measured using Shorr lengthboards (Shorr Productions, Olney, Md.) to within 0.1 cm. Fordehydrated children the examination was repeated after hydration.Stunting was defined as a z score of less than -2 for lengthor height for age (indicating a value more than 2 SD below themedian for the reference population) and wasting as a z scoreof less than -2 for weight for length; the reference populationused was that of the National Center for Health Statistics.25
A venous blood sample for the estimation of zinc levels wascollected with Monovette trace elementfree heparinizedsyringes (Sarstedt, Newton, N.C.); plasma was separated within15 minutes after collection of samples. Zinc was analyzed withstandard methods.26
Randomization and Blinding
Randomization schedules with permuted blocks of 1027,28 wereused for children with four combinations of characteristics:those with z scores of -2 or greater for weight for length whowere partially or exclusively breast-fed (stratum A1); thosewith z scores below -2 who were breast-fed (A2); those withz scores of -2 or greater who were not breast-fed (A3); andthose with z scores below -2 who were not breast-fed (A4). Withineach stratum, enrolled children were assigned sequential serialnumbers indicating whether they would receive the zinc preparationor placebo. The solutions were identical in appearance and taste.The code, which was kept by WHO personnel, was not availableto the investigators until the end of the study.
Intervention
The liquid preparations given to the children in the two groupswere made by Sandoz India (Bombay). Each daily 10-ml dose containedvitamins A (1600 units), B1 (1.2 mg), B2 (1.0 mg), B6 (1.0 mg),D3 (200 IU), and E (6 mg) and niacinamide (20 mg). The zincpreparation contained zinc gluconate (20 mg of elemental zinc).Bottles were given to each child's mother and kept at home.A separate team of field assistants dispensed the assigned preparationto the child in the home every day except Sundays and holidays,when they left a measured dose in a separate vial for the motherto give to the child. Compliance was checked by other workerswho visited to assess the child's condition and by study supervisors.The supplement was actually fed by the field worker on 78 percentof the days in the zinc-supplementation group and 79 percentof the days in the control group; on 2 to 3 percent of the daysin each group no supplement was consumed.
Follow-Up Visits
Each enrolled child was visited at home by a trained field workerevery fifth day, and information for each of the previous fivedays, including the number and consistency of stools, was recorded.Children who were unavailable were visited again the next day.Mothers were asked to contact the study physicians at the clinicif they felt that their children were sick between the visits.Packets of oral rehydration salts were provided by the fieldworker, and the mother was advised about treating the child'sdiarrhea. Parents were given a card to show to any non-studyhealth worker stating that the child should not be given anyadditional vitamin or mineral preparation. Children who haddysentery or who had diarrhea for 10 days or more after enrollmentwere given antibiotics. None of the medications used containedzinc.
Study Groups
Of 960 children screened, 13 were excluded because their parentsdid not give consent; no child was excluded because of malnutrition.A total of 947 children were assigned to treatment groups: 462to the zinc-supplementation group and 485 to the control group;576 were from stratum A1, 177 from A2, 143 from A3, and 51 fromA4. Ten children were excluded from analysis (six in the zincgroup and four in the control group); in five cases consentwas withdrawn at the first home visit, in two the diarrhea stoppedbefore supplementation could be begun, and in three there wasmissing information for two or more consecutive visits. Forsix children, three in each group, the total duration of diarrheawas unknown; they were included in the survival analysis butnot in analyses of the total duration of diarrhea. In eightcases, consent to collect a blood sample for the estimationof the zinc concentration was refused.
Definitions of Primary Outcomes
A day of diarrhea was defined as the passage of four or moreunformed stools in 24 hours, and an episode of diarrhea wasconsidered terminated on the last day of diarrhea that was followedby a 72-hour diarrhea-free period. A day with watery stoolswas defined as the passage of three or more watery stools in24 hours.
Statistical Analysis
Statistical analysis was performed using SPSSPC+ (version 6.0),Epi-Info (version 6.0), and SAS (version 6.08) software. Relativerisks and 95 percent confidence intervals were estimated bythe Taylor series method.29 The total duration of episodes wasmodeled with Cox survival regressions with a time-dependentcovariate (PHREG in SAS 6.07 on a VMS mainframe had to be usedto enable the use of the "exact option" for the handling ofties).30,31 The time-dependent covariate was assigned a valueof 0 (for children in the control group) or 1 (for those inthe zinc-supplementation group) on the day that supplementationbegan. In addition, a second model that allowed the effect ofsupplementation to change between days 1 through 3 and day 4or later after the beginning of supplementation32 was fittedwith two time-dependent variables. Finally, logistic-regressionmodels used the duration of diarrhea (>7 days vs. <7 days)from the time of enrollment as the dependent variable; the treatmentgroup, potential covariates, and interaction terms were theindependent variables.27
Results
The base-line characteristics of the children in the two groupswere similar (Table 1). Identical proportions (0.4 percent)were exclusively breast-fed. One child in each group was initiallyhospitalized for the treatment of dehydration. Among socioeconomicindicators, the average annual incomes (about $532) and therate of ownership of a number of household items (data not shown)were similar in the two groups.
Table 1. Base-Line Demographic Characteristics and Features of the Episodes of Diarrhea, According to Study Group.
Duration of Episodes of Diarrhea
Of 931 episodes of diarrhea, 44.4 percent resolved within threedays after enrollment, and 83.5 percent resolved by day 7. Supplementationwith zinc was associated with a 23 percent reduction in therisk of continued diarrhea on a given day (model 1 in Table 2).For the subgroups of children who had stunted growth orlow plasma zinc concentrations at enrollment, the reductionsin risk were 25 percent and 27 percent, respectively (model1). In a model including stunting, age group, and plasma zincconcentration as covariates (model 2 in Table 2), zinc supplementationwas associated with a 21 percent reduction in the risk of continueddiarrhea.
Table 2. Relative Risk of Continued Diarrhea in the Cox Regression Models, According to Study Group.
KaplanMeier curves (data not shown), although they didnot take into account the duration of diarrhea before enrollment,indicated that the reduction in the duration of diarrhea becameevident on the fourth day after the beginning of supplementation.Therefore, we used a model that included the effect of supplementationfor days 1 through 3 and for day 4 and subsequent days; theresulting fit was better than with model 1.32 The estimatedrelative risk of continued diarrhea in the zinc-supplementationgroup as compared with the control group was 0.93 (95 percentconfidence interval, 0.78 to 1.09) during days 1, 2, and 3 ofsupplementation and 0.62 (95 percent confidence interval, 0.52to 0.73) after day 3.
Persistence and Severity of Diarrhea
In the zinc-supplementation group there was a significant reduction(39 percent) in episodes of diarrhea lasting more than sevendays after enrollment when supplementation was started withinthree days of the onset of diarrhea (Table 3). To evaluate theeffect of supplementation in a multivariate analysis, we useda logistic-regression model in which the dependent variablewas the duration of diarrhea (<7 vs. >7 days from theonset of treatment); sex, the use of a drug during the episode(yes or no), breast-feeding (yes or no), years of schoolingof the child's mother, study group (zinc supplementation orcontrol), z score for height for age (< -2.0 or -2.0), andthe plasma zinc concentration (<60.0 or 60.0 µg perdeciliter [<9.2 or 9.2 mmol per liter]) were entered as independentvariables. In this model, the odds ratio for diarrhea lastingmore than seven days was 0.79 with zinc supplementation (95percent confidence interval, 0.64 to 0.96). The odds ratio was0.74 (95 percent confidence interval, 0.57 to 0.95) when themodel was restricted to the children enrolled by day 3 of theepisode of diarrhea.
Table 3. Frequency of Diarrhea Lasting More than Seven Days and Severity of Episodes of Diarrhea, According to Study Group.
There was a 39 percent reduction (95 percent confidence interval,6 percent to 70 percent) in the mean number of watery stoolsper day in the zinc-supplementation group (P = 0.02) and a 21percent reduction (95 percent confidence interval, 10 percentto 31 percent) in the number of days with watery stools. Inthe zinc-supplementation group the mean (±SD) numberof watery stools per day was 3.1±9.9, as compared with5.1±14.9 in the control group. Fewer children in thezinc-supplementation group were taken to a physician at leastonce during follow-up because their parents were concerned abouttheir health, but this difference was not significant (P = 0.12).
Analyses of Subgroups
The reduction in the likelihood of diarrhea lasting more thanseven days was 65 percent in the subgroup of children with stuntedgrowth who had had diarrhea for less than four days before enrollment(Table 4). The effect of zinc on the number of days with waterystools was greater in children with stunted growth than in thosewith normal growth (relative risk in the zinc-supplementationgroup as compared with the controls, 0.59 [95 percent confidenceinterval, 0.48 to 0.73] and 0.95 [95 percent confidence interval,0.79 to 1.15], respectively). In children with wasting (z scorefor weight for length < -2), there was an even greater reductionin the number of days of watery diarrhea (relative risk in thezinc-supplementation group, 0.48; 95 percent confidence interval,0.39 to 0.68). There was no clear trend with respect to theeffect within subgroups defined according to the plasma zinclevels.
Table 4. Duration and Severity of Episodes of Diarrhea among Children with Stunted Growth and Children with Plasma Zinc Levels ,60 mg/dl at Enrollment, According to Study Group.
Adverse Reactions
Four children, two in each group, reported vomiting immediatelyafter consuming the supplement on one or two occasions.
Discussion
This study, conducted in New Delhi, documents the effectivenessof zinc supplementation as an adjunct to oral rehydration therapyand early continued feeding among preschool children with acutediarrhea. Zinc supplementation was associated with a clinicallyimportant and statistically significant overall reduction of23 percent in the risk of continued diarrhea and a 39 percentreduction in the frequency of episodes persisting more thanseven days after treatment began. It also resulted in a 21 percentreduction in the number of days with watery stools and a 39percent reduction in the mean number of watery stools per day.Reductions in the frequency of prolonged diarrhea and the numberof days with watery stools may decrease the risk of dehydrationand the need for fluid and electrolyte replacement. We couldnot measure the effect of zinc supplementation on dehydrationbecause oral-rehydration solution was provided from the dayof enrollment. Reductions in the frequency of diarrhea may alsoimprove growth.33
Because the study was conducted with the children at home ratherthan in the hospital, they were able to continue their usualdiets. We made relatively few visits to assess morbidity, sothat the natural history of the illness could be evaluated withoutintensive medical intervention, although this practice mighthave limited the precision of the information on daily outcomes.
In a previous trial of supplementation with 20 mg of zinc dailyin children with acute diarrhea, there were no differences inoutcomes overall, but the children with low zinc concentrationsin the rectal mucosa had shorter episodes of diarrhea and lessfrequent stools.34 In a small study of children with persistentdiarrhea, the administration of a 20-mg zinc supplement wasassociated with a 20 percent reduction in the duration of diarrheaand the frequency of stools, although these differences werenot statistically significant.35
The finding of a sizable effect of supplementation and the observationthat 37 percent of the children with diarrhea had plasma zinclevels below 60 µg per deciliter suggest a high prevalenceof zinc deficiency in this population. Since the plasma zinclevel was measured during the episode of diarrhea, a transienteffect of the episode on plasma zinc levels cannot be eliminated36,37,38,39,40,41,42;however, similar plasma zinc levels were found in the studychildren who did not receive the supplement 120 days after episodesof diarrhea (unpublished data). Studies from other developingcountries suggest that dietary zinc deficiency can be highlyprevalent among preschool-age children.22,23 The diets of youngchildren in our Indian study population share two characteristicswith other zinc-deficient populations: a low intake of meator dairy products, which contain zinc, and a high intake ofphytates, which interfere with the bioavailability of zinc.
The comparison of the effects of supplementation among subgroupsindicates that stunting, wasting, or both can be used to selectthe children most likely to benefit from treatment with zinc.The initial plasma zinc level did not differentiate those whowould derive greater benefit from supplementation from thosewho would benefit less.
The possible mechanisms for the effect of zinc supplementationon diarrhea include improved absorption of water and electrolytesby the intestines,43,44,45,46,47,48,49 regeneration of gut epitheliumor the restoration of its function,50,51,52,53,54,55,56,57,58increased levels of enterocyte brush-border enzymes,59,60,61,62,63,64,65and enhanced immunologic mechanisms for the clearance of infection,including cellular immunity and higher levels of secretory antibodies.66,67,68It is also possible that improved appetite and dietary intakeresulted in shorter episodes of diarrhea, as a result of theeffect of staple foods on stool consistency.69
In conclusion, a dietary supplement of zinc, along with selectedvitamins, resulted in clinically important reductions in theduration and severity of diarrhea among preschool-age children.Because these findings may have important implications for thereduction of morbidity and mortality due to diarrhea in children,they need to be confirmed in other developing countries.
Supported by the World Health Organization, Diarrheal DiseaseControl Program, the Thrasher Research Fund, and the IndianCouncil for Medical Research. Dr. Sazawal is the recipient ofa fellowship from the Rockefeller Foundation.
We are indebted to Dr. Michael Hambidge and Jaime Westcott forhelp with the estimation of plasma zinc levels; to Dr. LarryMoulton for statistical advice; to Dharminder Kashyap and UshaDhingra for data management; to the field staff of the projectand the parents of the participating children for their assistance;to Sandoz India, Ltd., for the supplements; and especially toDr. Ashok Agarwal for preparing the supplements, maintainingtheir quality, and ensuring delivery.
Source Information
From the Department of International Health, School of Hygiene and Public Health, Johns Hopkins University, Baltimore (S.S., R.E.B.), and the Indian Council for Medical Research Advanced Center for Diarrheal Disease Research, Division of Pediatric Gastroenterology, All India Institute of Medical Sciences, New Delhi, India (S.S., M.K.B., N.B., A.S., S.J.).
Address reprint requests to Dr. Black at 615 N. Wolfe St., Baltimore, MD 21205.
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