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Nonscarring scalp alopecia: Which laboratory analysis should we perform on whom?

Ümran Öner, Necmettin Akdeniz
Other Turkish journal of medical sciences 2022 8 citations
PubMed DOI CC-BY PDF
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Study Design

Type d'étude
retrospective cross-sectional study
Taille de l'échantillon
467
Intervention
Nonscarring scalp alopecia: Which laboratory analysis should we perform on whom? not applicable
Comparateur
Placebo
Direction de l'effet
Mixed
Risque de biais
Moderate

Abstract

BACKGROUND: Vitamins and minerals are thought to play an essential but not entirely clear role in developing, preventing, and treating nonscarring alopecia. Telogen effluvium, androgenetic alopecia, and alopecia areata are the most common forms of nonscarring alopecias. We would like to present a different perspective on laboratory abnormalities in patients with nonscarring alopecia. METHODS: A total of 467 patients (287 females, 180 males) were included retrospectively: One hundred and sixty patients in the telogen effluvium group, 101 patients in the androgenetic alopecia group, 99 patients in the alopecia areata group, and 107 patients in the hair loss group (patients who could not be diagnosed with any nonscarring alopecia and wanted to have an analysis due to the complaint of hair loss). Sociodemographic data, diagnostic distribution, and laboratory findings (hemoglobin, ferritin, vitamin B12, vitamin D, and TSH) were evaluated and compared. RESULTS: The most common diagnosis was telogen effluvium in females and androgenetic alopecia in males. In women, hemoglobin (12.2% vs. 1.1%) and ferritin deficiencies (22.3% vs. 8.9%) were significantly higher than in men (p < 0.001, p < 0.001) Ferritin, hemoglobin, and vitamin B12 levels were significantly lower, and the number of patients with vitamin D, ferritin, hemoglobin and vitamin B12 deficiencies were significantly higher in the telogen effluvium group compared to the other groups. Laboratory abnormalities were detected least in the hair loss group.

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Figures

Tables

Table 1

Age (years)Age range (years)FemaleMaleTotal
M ± SD n%n%n
TE 27.7 ± 8.8a7–5515697.5a42.5160
AGA 25.6 ± 7.3a15–502524.8b7675.2101
AA 26.1 ± 12.3a2–582525.3b7474.799
HL 21.4 ± 9.2b2–558175.7c2624.3107
Total 25.5 ± 9.72–5828761.418038.6467
p <0.001 * <0.001 **

Table 2

Vitamin D deficiencyHemoglobin deficiencyFerritin deficiencyVitamin B12 deficiencyThyroid dysfunction
n % n % n%n%n%
Female21574.93512.26422.33311.5227.7
Male 13072.221.1168.92111.7105.6
p * 0.519 <0.001 <0.001 0.9560.380

Table 3

Vitamin D (ng/mL)Hemoglobin (g/dL)Ferritin (ng/mL)Vitamin B12 (pg/mL)TSH (UI/mL)
M ± SDM ± SDM ± SDM ± SDM ± SD
TE 14.6 ± 11.1 13.5 ± 1.6 a 28.3 ± 37.4 a 317.7 ± 134.4 a 2.2 ± 1.6
AGA 16.2 ± 8.416.1 ± 1.4b100.0 ± 84.7b 316.8 ± 170.5 a 2.1 ± 1.4
AA 15.7 ± 9.615.4 ± 1.5c93.5 ± 103.9b344.6 ± 150.4a,b2.3 ± 2.0
HL 17.9 ± 11.314.8 ± 1.4d59.3 ± 47.6c377.1 ± 154.9b2.2 ± 1.1
p * 0.086 <0.001 <0.001 0.007 0.943

Table 4

Vitamin D deficiencyHemoglobin deficiencyFerritin deficiencyVitamin B12 deficiencyThyroid dysfunction
n%n% n % n % n %
TE 127 79.4 a 32 20.0 a 53 33.1 a 32 20.0 a 159.4
AGA 79 78.2 a,b 00.0b87.9b1110.9a,b65.9
AA 70 70.7 a,b 44.0b1313.1b88.1a,b88.1
HL 6964.5b10.9b6 b5.6b32.8b32.8
p * 0.031 <0.001 <0.001 <0.001 0.194

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