Investigation of transient hypogammaglobulinemia of infancy in the
etiology of chronic cough in children under five years old
Mehmet Fatih Alptekin1, Gökçen
Ünal2, Aslı İmran Yılmaz2, Hanife
Tuğçe Çağlar2, Fatih Ercan2, Sevgi
Keleş3, İsmail Reisli3, Sevgi
Pekcan2 *
- Necmettin Erbakan University Meram Medical Faculty, Department of
Pediatrics
- Necmettin Erbakan University Meram Medical Faculty, Division of
Pediatric Chest Diseases
- Necmettin Erbakan University Meram Medical Faculty, Division of
Pediatric Immunology and Allergy
Abstract
Chronic cough is one of the most common complaints of childhood to
consult a doctor. There are many causes such as respiratory tract
infections, gastroesophageal reflux, persistent bacterial bronchitis,
asthma, cystic fibrosis, congenital malformations, and foreign body
aspiration in children under the age of five. However, neither transient
hypogammaglobulinemia of infancy (THI) among the causes of chronic
cough, nor chronic cough among the application complaints of THI are not
questioned. In this study, we aimed to draw attention to the role of THI
in the etiology of chronic cough under the age of five.
Our study included 55 pediatric patients under the age of five who
applied to the pediatric pulmonary diseases outpatient clinic in between
January 2015 and December 2020 with the complaint of chronic cough, who
were excluded from other causes of chronic cough in etiology, and who
met the criteria for THI according to the European Society for
Immunodeficiencies (ESID). Demographic, clinical and laboratory
characteristics and follow-ups of these patients were reviewed
retrospectively.
In our study, the mean age of 55 patients at admission was 21.73 ± 11.50
months (median age: 18 months), and the mean age of IgG recovery was
38.65 ± 16.81 months. The mean recovery time was 16.93 ± 12.85 months.
Of the patients, 22.4% had a history of consanguinity, 23.4% had
prematurity, and 18.2% had a frequent sickness in siblings. The most
common complaint accompanying chronic cough in patients was frequent
respiratory tract infection, 16.3%. Along with IgG, 26.4% of the
patients had low IgA and 31.5% had low IgM in laboratory testing. In
antibody responses, isohemagglutinin, anti-tetanus, anti-pneumococcal,
anti-HBs vaccine responses were found to be positive in 90.6%, 63.9%,
66.7% and 97.7% of the cases, respectively. 72.7% of the patients
received inhaler treatment, 45.5% received antibiotic prophylaxis, and
2.2% received intravenous immunoglobulin (IVIg) treatment. After the
IgG value of the patients returned to normal, it was observed that
86.3% of the patients’ cough complaint have disappeared.
Transient hypogammaglobulinemia of infancy mostly presents with
recurrent lower and upper respiratory tract infections. The most common
complaint is cough. It is not questioned whether the cough is chronic or
not. In this study, we aimed to investigate the follow-up and prognosis
of patients under the age of five who had a chronic cough complaint,
when other causes of cough were ruled out and THI was detected. In the
study, when the IgG levels of the patients return to normal, the cough
complaints disappear to a large extent, showing that THI may also be
among the causes of chronic cough.
Keywords: chronic cough, infant, transient hypogammaglobulinemia
Introduction
Cough is an important reflex that protects the airways from secretions
and foreign substances. It is the most common reason in pediatric
patients to seek for treatment all over the world. Prolonged coughing
reduces the quality of life of children and their families. Children’s
sleep patterns are disrupted and it becomes a source of stress for
parents. However, cough leads to frequent doctor visits and many
unnecessary examinations. In addition, excessive drug treatment causes a
serious increase in health expenditures 1,2.
The American College of Chest Physicians and the European Respiratory
Society define a cough that lasts longer than four weeks as a chronic
cough 3,4. Many factors are involved in the etiology
of chronic cough. Differential diagnosis is made according to the
patient’s symptoms accompanying cough, history and physical examination
findings. It can also be the first symptom of a simple upper respiratory
tract infection or a serious diseases such as cystic fibrosis (CF),
primary ciliary dyskinesia (PCD), immunodeficiency. Studies have shown
that recurrent viral infections, gastroesophageal reflux disease (GERD),
persistent bacterial bronchitis (PBB), asthma, transient whetting in
infants, congenital malformations, CF, PCD, and sinusitis are among the
most common causes of chronic cough in children under the age of five5-8. However, neither transient hypogammaglobulinemia
of infancy (THI) among the causes of chronic cough, nor chronic cough
among the complaints of THI are not questioned.
Transient hypogammaglobulinemia of the infancy is a primary
immunodeficiency characterized by a transient low serum IgG level. The
diagnosis is made when IgG value is below the normal value for age in
the first three years of life, defined causes of hypogammaglobulinemia
are excluded, and spontaneous resolution before 4 years of age (ESID
2019). In some patients, low IgG may be accompanied by low IgA and IgM.
Normal flow cytometric analyzes are a finding that supports THI.
Although the age of recovery of hypogammaglobulinemia is reported as 4
years, studies have also shown that the age of recovery extends up to
6-10 years 9-11.
Patients usually present with recurrent upper respiratory tract
infections, bronchiolitis, pneumonia, otitis, atopy; and less
frequently, diarrhea and urinary tract infections10,12,13. The most common complaint is cough. In the
etiology of THI, it is usually the nature of cough.
Generally, the nature and duration of cough are not questioned in the
etiology of THI. In our study, we aimed to retrospectively evaluate the
follow-up and prognosis of patients under the age of five who presented
with the complaint of chronic cough, and whose other causes of cough
were excluded.
Materials and Methods
Patient Selection
Our study included 55 pediatric patients aged 8 months to 5 years who
applied to the pediatric pulmonary diseases outpatient clinic with the
complaint of chronic cough between January 2015 and December 2020.
Demographic, clinical and laboratory characteristics and follow-ups of
these patients were reviewed retrospectively. Inclusion criteria; 1)
Patients whose other causes of chronic cough (GERD, PBB, etc.) have been
excluded, 2) Patients whose IgG value is below normal for age at
admission and who meet the definition of THI according to ESID criteria.
Exclusion criteria; Those with underlying immunodeficiency, congenital
anomalies, asthma, tuberculosis, CF, PCD, bronchiectasis and swallowing
dysfunction were excluded from the study.
None of the 11 patients with prematurity met the criteria for Broncho
Pulmonary Dysplasia, and the Ig values of the patients were evaluated
according to their corrected age 14. In our study, 603
of 1690 patients who applied with the complaint of cough resulted in low
IgG values. 460 of 603 patients were excluded from the study due to lack
of follow-up examination or comorbidities. 55 of 173 patients were
included in the study, as 17 of the remaining 143 patients had
lymphocyte subpopulations abnormalities and 71 did not have control IgG
(Figure 1).
Demographic characteristics of the patients, complete blood count, all
immunoglobulins, vaccine responses, and treatments were reviewed
retrospectively. It was evaluated whether the chronic cough improved
with the normalization of the immunoglobulin level. Ethic committee
approval was obtained for our study (23.09.2020 /2020/2854).
Statistical Analysis
All data were analyzed using SPSS 25.0 package program. Marginal
Homogeneity was used to compare the cases with more than two dependent
categories. Independent Group T-Test was used in the analysis of
independent paired groups of quantitative data. In the comparison of
quantitative data, in the case of more than two groups, the One-Way
ANOVA Test was used for intergroup comparisons of normally distributed
parameters, and the Kruskal Wallis Test for intergroup comparisons of
showing not normal distributed parameters. Post-hoc LSD Test was used in
the case of difference found between groups in the One-Way ANOVA Test.
In the study, p value <0.05 were accepted as statistically
significant.
Results
Demographic characteristics of 55 patients included in the study are
shown in Table 1.
The complaints accompanying chronic cough in the patients were frequent
respiratory tract infection with 16.3%, frequent bronchitis with
14.5%, wheezing with 12.7%, and pneumonia with 3.6%.
Mean IgG values of the patients according to age; 388.57 ± 56.67 for
9-12 months, 526.55 ± 63.41 for 13-24 months, 515.00 ± 53.81 for 25-36
months, 545.56 ± 58.68 for 37-48 months. The difference of IgG values
from the lower limit of normal values was determined according to the
age group and prematurity status of the patients, but no significant
result could be obtained regarding the difference (p>0.05).
When the laboratory values of the patients were examined; along with low
IgG in all patients, 26.4% had low IgA and 31.5% had low IgM. 12.7%
had anemia, 1.8% had neutropenia, 1.8% had eosinophilia, and 9.3% had
elevated IgE. When we look at specific antibodies, isohemagglutinin,
anti-tetanus, anti-pneumococcal, anti-HBs vaccine responses were found
to be positive in 90.6%, 63.9%, 66.7% and 97.7% of the cases,
respectively. Lymphocyte subpopulations were normal in all patients
(Table 2)
As treatment, 72.7% of the patients received inhaled corticosteroids,
45.5% received antibiotic prophylaxis, and 2.2% received IVIG. The
mean duration of inhaler treatment was 7.38 ± 10.1 months and the mean
duration of antibiotic prophylaxis was 5.55 ± 9.43 months. Duration of
inhaler treatment and antibiotic prophylaxis was at least 2 months and
at most 36 months (Table 3)
The IgG levels according to the age ranges of the patients are given in
Table 4 and the effect of age at presentation on the IgG recovery time
is given in Table 5.
During the follow-up period, 75% of the patients had bronchiolitis at
least once, and 77.2% of them were hospitalized for lower respiratory
tract infection (LRTI) at least once. The mean number of
hospitalizations (LRTI) was 2.43 ± 2.62, and the mean number of
bronchiolitis was 2.70 ± 2.87. There was no difference in the number of
hospitalizations due to LRTI, the number of previous bronchiolitis, the
duration of inhaler treatment and the duration of taking antibiotic
prophylaxis according to the age groups of patients (9-12 months, 13-24
months, 25-36 months, 37-48 months) (p> 0.05). None of the
patients was hospitalized when IgG reached normal values for age.
Thirty-eight (86.3%) of the patients no longer had a cough complaint
during IgG recovery. When the IgG reached the normal value for age, the
cough complaint of six patients continued for a maximum of one year
(1-12 months) after the IgG reached the normal value for the age, but
then improved.
Discussion
Among the most common causes of chronic cough etiology in children under
the age of five, there are recurrent viral infections, GERD, transient
whetting in infants, PBB, asthma, congenital malformations, CF, PCD, and
sinusitis. THI is not among these reasons.
While investigating the causes of cough in children aged 5 years who are
frequently sick, have recurrent respiratory tract infections and chronic
cough, it is also useful to evaluate the immune system15,16. Because more than 8 upper respiratory tract
infections (URTIs), and 2 or more previous pneumonia are the two of the
previous criteria of the Jeffrey Modell Foundation. We also looked at
the complete blood count and Ig’s as the first step tests for
immunodeficiency in children under 5 years old who presented with the
complaint of chronic cough. We retrospectively evaluated the follow-up
and prognosis of children under the age of five who had low IgG, other
immunodeficiencies were excluded, and the IgG level returned to the
normal range for age. Because, when we look at the literature, we could
not find any data on THI in the etiology of chronic cough in this age
group. Since it is known that immunological maturation is not the same
in every child, we thought that it may play a role in the etiology in
children under the age of five.
In patients under the age of five who have a chronic cough complaint,
other causes of cough have been ruled out, and we have detected THI; we
found that 86.3% of the patients no longer had a cough complaint after
their IgG value returned to normal. The complaints accompanying chronic
cough were frequent respiratory tract infection with 16.3%, frequent
bronchitis with 14.5%, wheezing with 12.7%, and pneumonia with 3.6%.
As treatment, 72.7% of the patients required inhaled corticosteroid,
45.5% required antibiotic prophylaxis, and 2.2% IVIG.
In the study of Yorulmaz et al., the age at diagnosis of THI varied
between 8 months and 48 months, with a mean of 24.6±11.3 months; Karaman
et al. found the mean age at diagnosis to be 11.7±7.0 months, with a
median of 10 months. In their study involving 30 patients, Doğu et al.
reported the age of diagnosis as 6-46 months (15 below 24 months, 12
24-36 months, 3 36-45 months), and the mean age was 22.5 months17-19. In our study, the mean age of THI detection in
children presenting with chronic cough was 21.73 ± 11.50 months; min –
max: 9 -47 months, which was consistent with the literature. 65% of the
applicants were in the first two years of age, and 16% were in the
range of 36-47 months. We thought that the prolongation of the admission
age was due to the fact that the patients went to different centers with
the complaint of chronic cough until they came to us.
In a large-scale study on patients with primary immunodeficiency (PID)
in Turkey, the prevalence of PID was found to be 30.5/100,000. The
reason why this rate is higher than in Europe is the high rate of
consanguineous marriages in our country 20. In our
patients, 22.4% had parental consanguinity. Yorulmaz et al. found the
rate of consanguineous marriage as 30% in their study17.
While clinically asymptomatic in THI, it can also be seen as a very
serious invasive infection. However, most of the studies have reported
that the most common reason for admission is respiratory tract
infections. Yorulmaz et al. reported 54% recurrent URTI, 50% LRTI,
41% sinusitis, 28% recurrent otitis in a study involving 287 cases17. Keleş et al. most frequently 53% LRTI, 39% URTI;
Doğu et al. reported 93% recurrent URTI, 26% pneumonia, 26% otitis10,19. Karaca et al. reported that 70.3% of 101
patients with THI presented with recurrent URTI findings, 6.9% had
recurrent wheezing attacks and 8.9% presented with LRTI11. In our study, in addition to chronic cough, we
found 16,3% had frequent respiratory tract infections, 14.5% had
frequent bronchitis, 12.7% had wheezing and 3.6% had pneumonia. These
studies are important in terms of emphasizing the role of THI in the
etiology of chronic cough. In these studies, cough durations were not
defined in the complaint. For this reason, chronic cough is not
mentioned in the literature among the complaints of THI. However, it
should be kept in mind that cough is the most typical complaint of URTI
and LRTI and this cough can last up to 8 weeks.
Low IgG can be accompanied by low IgM and IgA in THI21. It was found that 26.4% of our patients had low
IgA and 31.5% had low IgM along with low IgG in our patients. In the
study of Keleş et al., they found low IgA in 28.1% of the patients and
low IgM in 23.4% 10. In the study of Doğu et al., it
was found that all of the patients had low IgG along with low IgA in
43% and IgM in 20%; and they reported that lymphocyte subpopulations
were measured in 20 patients and all of them were normal19. In our study, low IgA and IgG levels were found to
be compatible with the literature.
In our study, seven patients (12.7%) had anemia, one patient (1.8%)
had neutropenia, one patient (1.8%) had eosinophilia, and five patients
(9.3%) had elevated IgE. Only one of our patients had milk positivity
in the skin prick test and the IgE value was the highest. Yorulmaz et
al. included 287 patients with anemia in 108 patients (37.63%),
neutropenia in 11 patients (3.83%), and lymphopenia in four patients
(1.39%) 17. In our study, anemia and neutropenia were
lower than in the literature. We did not detect lymphopenia in any of
our patients.
Improvement in THI usually takes place up to 3 years of age. In the ESID
2019 guideline, it has been accepted as a criterion to be before the age
of 4 as an improvement. However, there are studies indicating that this
period may be much longer. In one study, it was found that only 25% of
the cases recovered before the age of 3, and the mean recovery age was
68.87 ± 36.5 months (min: 20 months, max: 192 months)10. In their study, Kütükçüler et al. reported that Ig
levels improved at an average of 5 years (62.5±21.8 months), while Dalal
et al. reported that the improvement in IgG extended up to 10 years13,22. In our study, the mean age of recovery was
38.65 ± 16.81 months; min-max: 14-78 months; mean recovery time was
16.93 ± 12.85 months; min-max: 3-47 months.
Supportive and infection-oriented symptomatic treatment is given as
treatment in THI. Antibiotic prophylaxis is preferred in case of
recurrent infections. Rarely, IVIG treatment can be considered in severe
infections that do not respond to antibiotics 23. In
our study, 72.7% of the patients were treated with inhaled
corticosteroids and 45.5% with prophylactic antibiotics (trimethoprim
(5 mg/kg) –sulfamethoxazole) as a single dose three days a week
received. Only one patient (2.2%) received 5 doses of IVIG every 3
weeks due to recurrent pneumonia.Yorulmaz et al. administered
trimethoprim-sulfamethoxazole prophylaxis to 129 of 287 cases (44.9%),
and IVIG treatment to 2 patients (0.69%) 17. Kidon et
al. reported that four (23.5%) of 17 patients received antibiotic
prophylaxis and two (11.7%) received IVIG 24. Doğu et
al. reported two (6.6%) of 30 patients, Kılıç et al. reported that two
out of 40 patients (5%) needed short-term IVIG treatment9,19.
In our study, during the IgG recovery period, 77.2% of the patients had
a history of hospitalization due to LRTI and a history of bronchiolitis
in 75%. The maximum number of hospitalizations was 10. This was the
patient who used the longest inhaler and antibiotic prophylaxis. None of
the patients were hospitalized after IgG recovery. When IgG improved,
86.3% of the patients did not have a cough complaint. After the IgG
levels of the patients whose cough continued, the cough complaint
completely disappeared within one year at the latest. This made us think
that THI may play a role in the etiology of chronic cough in infancy and
should be investigated in the etiology. The improvement of the patients’
IgG and the disappearance of chronic cough supports our thesis. .
The limitations of our study; 1) due to the retrospective nature of our
study, all causes of chronic cough in children under the age of five
could not be identified separately, 2) where was a lack of data due to
the fact that the information was obtained from the patient registry
files, 3) we excluded the patients who were thought to have THI but
could not see improved IgG because they did not come to the follow-up,
which reduced total number of THI patients, 4) not showing for
appoinements in patients after cough complaints have improved, 5) the
disruption of outpatient services due to the COVID-19 pandemic and the
prolongation of the follow-up periods due to the patients’ reluctance to
come for control.
In conclusion; THI should be considered in recurrent URTI and LRTI under
the age of five. Cough is the most common complaint in these patients.
There is no information in the literature about THI in the etiology of
chronic cough. Our study predicts that THI may be involved in the
etiology in chronic cough. This study is of a preliminary nature, and
the continuation of the prospective study is planned. Prospective
studies with a much higher number of patients are needed in this regard.
References
1. Shields MD, Bush A, Everard ML, McKenzie S, Primhak R.
Recommendations for the assessment and management of cough in children.Thorax. 2008;63(Suppl 3):iii1-iii15.
2. Marchant JM, Newcombe PA, Juniper EF, Sheffield JK, Stathis SL, Chang
AB. What is the burden of chronic cough for families? Chest.2008;134(2):303-309.
3. Morice AH, Millqvist E, Bieksiene K, et al. ERS guidelines on the
diagnosis and treatment of chronic cough in adults and children.European respiratory journal. 2020;55(1).
4. Chang AB, Oppenheimer JJ, Irwin RS, et al. Managing chronic cough as
a symptom in children and management algorithms: CHEST Guideline and
Expert Panel Report. Chest. 2020;158(1):303-329.
5. Wagner JB, Pine HS. Chronic cough in children. Pediatric
clinics of North America. 2013;60(4):951-967.
6. Chang AB, Redding G, Everard M. Chronic wet cough: protracted
bronchitis, chronic suppurative lung disease and bronchiectasis.Pediatric pulmonology. 2008;43(6):519-531.
7. Çakır E, Uzuner S, Erenberk U, et al. Evaluation of 563 children with
chronic cough acompanied by a new clinical algorithm. 2016.
8. Alsubaie H, Al-Shamrani A, Alharbi AS, Alhaider S. Clinical practice
guidelines: Approach to cough in children: The official statement
endorsed by the Saudi Pediatric Pulmonology Association (SPPA).International journal of pediatrics & adolescent medicine.2015;2(1):38-43.
9. Kiliç SŞ, Tezcan İ, Sanal Ö, Metin A, Ersoy F. Transient
hypogammaglobulinemia of infancy: clinical and immunologic features of
40 new cases. Pediatrics International. 2000;42(6):647-650.
10. Keles S, Artac H, Kara R, Gokturk B, Ozen A, Reisli I. Transient
hypogammaglobulinemia and unclassified
hypogammaglobulinemia:‘similarities and differences’. Pediatric
allergy and immunology. 2010;21(5):843-851.
11. Karaca NE, Aksu G, Gulez N, Yildiz B, Azarsiz E, Kutukculer N. New
laboratory findings in Turkish patients with transient
hypogammaglobulinemia of infancy. Iranian Journal of Allergy,
Asthma and Immunology. 2010:237-243.
12. Qian JH, Zhu JX, Zhu XD, Chen TX. Clinical features and follow-up of
Chinese patients with symptomatic hypogammaglobulinemia in infancy.Chin Med J (Engl). 2009;122(16):1877-1883.
13. Dalal I, Reid B, Nisbet-Brown E, Roifman CM. The outcome of patients
with hypogammaglobulinemia in infancy and early childhood. J
Pediatr. 1998;133(1):144-146.
14. Poindexter BB, Feng R, Schmidt B, et al. Comparisons and Limitations
of Current Definitions of Bronchopulmonary Dysplasia for the Prematurity
and Respiratory Outcomes Program. Annals of the American Thoracic
Society. 2015;12(12):1822-1830.
15. Owayed AF, Campbell DM, Wang EE. Underlying causes of recurrent
pneumonia in children. Archives of pediatrics & adolescent
medicine. 2000;154(2):190-194.
16. Munteanu AN, Surcel M, Huică RI, et al. Peripheral immune cell
markers in children with recurrent respiratory infections in the absence
of primary immunodeficiency. Experimental and therapeutic
medicine. 2019;18(3):1693-1700.
17. Yorulmaz A, Artaç H, Reisli İ. Evaluation of patient follow-up with
transient hypogammaglobulinemia in infancy diagnosis. Çağdaş Tıp
Dergisi. 2019;9(1):15-20.
18. Karaman S, Gulez N, Bahceci Erdem S, Nacaroglu HT, Genel F. Five
years of experience in transient hypogammaglobulinemia of infancy.Izmir Dr Behcet Uz Cocuk Hastanesi Dergisi. 2016;6(3):209-214.
19. Doğu F, Ikincioğullari A, Babacan E. Transient hypogammaglobulinemia
of infancy and early childhood: outcome of 30 cases. Turk J
Pediatr. 2004;46(2):120-124.
20. Kilic SS, Ozel M, Hafizoglu D, Karaca NE, Aksu G, Kutukculer N. The
Prevalances and patient characteristics of primary immunodeficiency
diseases in Turkey—Two centers study. Journal of clinical
immunology. 2013;33(1):74-83.
21. Siemińska I, Rutkowska-Zapała M, Bukowska-Strakova K, et al. The
level of myeloid-derived suppressor cells positively correlates with
regulatory T cells in the blood of children with transient
hypogammaglobulinaemia of infancy. Central-European journal of
immunology. 2018;43(4):413-420.
22. Kutukculer N, Gulez N. The outcome of patients with unclassified
hypogammaglobulinemia in early childhood. Pediatric allergy and
immunology. 2009;20(7):693-698.
23. Justiz Vaillant AA, Wilson AM. Transient Hypogammaglobulinemia of
Infancy. In: StatPearls. Treasure Island (FL): StatPearls
Publishing
Copyright © 2021, StatPearls Publishing LLC.; 2021.
24. Kidon MI, Handzel ZT, Schwartz R, Altboum I, Stein M, Zan-Bar I.
Symptomatic hypogammaglobulinemia in infancy and childhood–clinical
outcome and in vitro immune responses. BMC Family Practice.2004;5(1):1-7.
Tables:
Table 1. The demographic characteristics of the patients
Table 2. Laboratory findings of the patients
Table 3. Clinical characteristics of the patients
Tablo 4. Descriptive information on IgG levels according to age ranges
of patients
Table 5. Comparison of follow-up time according to age group of patients
Figure
Figure 1. Flow chart