Localized alopecia and suppression of hypothalamic-pituitary-adrenal
Background Despite the common use of topical ophthalmic corticosteroids in dogs, detailed reports on systemic and dermatologic adverse effects are limited. Results Nine purpose-bred research Beagles were treated with difluprednate 0.05% ophthalmic emulsion in one or both eyes 2-3 times daily. Some d...
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creator | Quantz, Katelin Anderson, Amanda L Harman, Christine D Noland, Erica L Del Valle, Jacquelyn M Occelli, Laurence M Burn, Jessica B Petersen-Jones, Simon M Langlois, Daniel K Pirie, Chris G Petersen, Annette D Komáromy, András M |
description | Background Despite the common use of topical ophthalmic corticosteroids in dogs, detailed reports on systemic and dermatologic adverse effects are limited. Results Nine purpose-bred research Beagles were treated with difluprednate 0.05% ophthalmic emulsion in one or both eyes 2-3 times daily. Some difluprednate treated dogs developed mild to severe alopecia of the periocular region, face, and distal pinna (5/9). The median duration of treatment prior to onset of dermatologic signs for difluprednate treated dogs was 550 days (453-1160 days). Diagnostic testing included complete blood count (CBC) and serum biochemistry, adrenocorticotropic hormone (ACTH) stimulation testing combined with endogenous ACTH measurement, and skin biopsy. The CBC and chemistry were within normal limits for all dogs. There were varying degrees of suppression of the hypothalamic-pituitary-adrenocortical (HPA) axis with difluprednate treatment. Dogs with the most profound alopecic changes had less pronounced HPA axis suppression compared to dogs with no integumentary changes. Skin biopsies demonstrated follicular atrophy and follicular keratosis. When topical difluprednate was reduced to unilateral therapy, the hair regrew on the untreated side of the face. In addition to the affected research dogs, a 7-year old female spayed Chihuahua that was being treated as a clinical patient with long-term difluprednate 0.05% ophthalmic emulsion developed generalized hypotrichosis on the head and body and a potbellied appearance. ACTH stimulation testing revealed suppression of the HPA axis with a mild increase in serum alkaline phosphatase (ALP) activity and a urine specific gravity of 1.016. The combination of clinical signs and laboratory abnormalities was supportive of iatrogenic hyperadrenocorticism. Conclusions In dogs long-term use of difluprednate ophthalmic emulsion results in HPA axis suppression and in some cases iatrogenic hyperadrenocorticism. A novel pattern of localized alopecia is suspected to be related to dermal absorption and local action due to superior potency and penetration compared to other commonly utilized ophthalmic corticosteroids. Keywords: Alopecia, Canine, Corticosteroids, Difluprednate (Durezol[R]), Follicular atrophy, Hypothalamic-pituitary-adrenocortical (HPA) axis, Ophthalmic |
doi_str_mv | 10.1186/s12917-021-03072-9 |
format | Article |
fullrecord | <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_infotracmisc_A686393260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A686393260</galeid><sourcerecordid>A686393260</sourcerecordid><originalsourceid>FETCH-LOGICAL-g670-7d88c71424db4afb6c9069631c4adfbc2fcb5585f157c89a92c2e7ff89b804853</originalsourceid><addsrcrecordid>eNptTs1KAzEYDKJgrb6ApwXPqUk2m59jqVqFgpfey7dfkjaSbpbN9lCf3gU99CBzmGGYGYaQR84WnBv1XLiwXFMmOGU104LaKzLjWiqquDTXF_qW3JXyxZiUVqsZedlkhBS_vasg5d5jhAo6V5VT3w--lJi7KofqcO7zeIAEx4i0j-MpjjCcKbjBd5DuyU2AVPzDH8_J9u11u3qnm8_1x2q5oXulGdXOGNRcCulaCaFVaJmyquYowYUWRcC2aUwTeKPRWLAChdchGNsaJk1Tz8nT7-wekt_FLuRxADzGgrulMqq2tVBsSi3-SU1wfjqfOx_i5F8UfgCdHl2B</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Localized alopecia and suppression of hypothalamic-pituitary-adrenal</title><source>SpringerLink Journals</source><source>TestCollectionTL3OpenAccess</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><source>Springer Nature OA Free Journals</source><creator>Quantz, Katelin ; Anderson, Amanda L ; Harman, Christine D ; Noland, Erica L ; Del Valle, Jacquelyn M ; Occelli, Laurence M ; Burn, Jessica B ; Petersen-Jones, Simon M ; Langlois, Daniel K ; Pirie, Chris G ; Petersen, Annette D ; Komáromy, András M</creator><creatorcontrib>Quantz, Katelin ; Anderson, Amanda L ; Harman, Christine D ; Noland, Erica L ; Del Valle, Jacquelyn M ; Occelli, Laurence M ; Burn, Jessica B ; Petersen-Jones, Simon M ; Langlois, Daniel K ; Pirie, Chris G ; Petersen, Annette D ; Komáromy, András M</creatorcontrib><description>Background Despite the common use of topical ophthalmic corticosteroids in dogs, detailed reports on systemic and dermatologic adverse effects are limited. Results Nine purpose-bred research Beagles were treated with difluprednate 0.05% ophthalmic emulsion in one or both eyes 2-3 times daily. Some difluprednate treated dogs developed mild to severe alopecia of the periocular region, face, and distal pinna (5/9). The median duration of treatment prior to onset of dermatologic signs for difluprednate treated dogs was 550 days (453-1160 days). Diagnostic testing included complete blood count (CBC) and serum biochemistry, adrenocorticotropic hormone (ACTH) stimulation testing combined with endogenous ACTH measurement, and skin biopsy. The CBC and chemistry were within normal limits for all dogs. There were varying degrees of suppression of the hypothalamic-pituitary-adrenocortical (HPA) axis with difluprednate treatment. Dogs with the most profound alopecic changes had less pronounced HPA axis suppression compared to dogs with no integumentary changes. Skin biopsies demonstrated follicular atrophy and follicular keratosis. When topical difluprednate was reduced to unilateral therapy, the hair regrew on the untreated side of the face. In addition to the affected research dogs, a 7-year old female spayed Chihuahua that was being treated as a clinical patient with long-term difluprednate 0.05% ophthalmic emulsion developed generalized hypotrichosis on the head and body and a potbellied appearance. ACTH stimulation testing revealed suppression of the HPA axis with a mild increase in serum alkaline phosphatase (ALP) activity and a urine specific gravity of 1.016. The combination of clinical signs and laboratory abnormalities was supportive of iatrogenic hyperadrenocorticism. Conclusions In dogs long-term use of difluprednate ophthalmic emulsion results in HPA axis suppression and in some cases iatrogenic hyperadrenocorticism. A novel pattern of localized alopecia is suspected to be related to dermal absorption and local action due to superior potency and penetration compared to other commonly utilized ophthalmic corticosteroids. Keywords: Alopecia, Canine, Corticosteroids, Difluprednate (Durezol[R]), Follicular atrophy, Hypothalamic-pituitary-adrenocortical (HPA) axis, Ophthalmic</description><identifier>ISSN: 1746-6148</identifier><identifier>EISSN: 1746-6148</identifier><identifier>DOI: 10.1186/s12917-021-03072-9</identifier><language>eng</language><publisher>BioMed Central Ltd</publisher><subject>Alopecia ; Baldness ; Causes of ; Complications and side effects ; Cushing syndrome ; Difluprednate ; Diseases ; Dogs ; Dosage and administration ; Drug therapy ; Health aspects ; Hypothalamic-pituitary-adrenal axis ; Ophthalmic drugs ; Uveitis</subject><ispartof>BMC veterinary research, 2021-12, Vol.17 (1)</ispartof><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Quantz, Katelin</creatorcontrib><creatorcontrib>Anderson, Amanda L</creatorcontrib><creatorcontrib>Harman, Christine D</creatorcontrib><creatorcontrib>Noland, Erica L</creatorcontrib><creatorcontrib>Del Valle, Jacquelyn M</creatorcontrib><creatorcontrib>Occelli, Laurence M</creatorcontrib><creatorcontrib>Burn, Jessica B</creatorcontrib><creatorcontrib>Petersen-Jones, Simon M</creatorcontrib><creatorcontrib>Langlois, Daniel K</creatorcontrib><creatorcontrib>Pirie, Chris G</creatorcontrib><creatorcontrib>Petersen, Annette D</creatorcontrib><creatorcontrib>Komáromy, András M</creatorcontrib><title>Localized alopecia and suppression of hypothalamic-pituitary-adrenal</title><title>BMC veterinary research</title><description>Background Despite the common use of topical ophthalmic corticosteroids in dogs, detailed reports on systemic and dermatologic adverse effects are limited. Results Nine purpose-bred research Beagles were treated with difluprednate 0.05% ophthalmic emulsion in one or both eyes 2-3 times daily. Some difluprednate treated dogs developed mild to severe alopecia of the periocular region, face, and distal pinna (5/9). The median duration of treatment prior to onset of dermatologic signs for difluprednate treated dogs was 550 days (453-1160 days). Diagnostic testing included complete blood count (CBC) and serum biochemistry, adrenocorticotropic hormone (ACTH) stimulation testing combined with endogenous ACTH measurement, and skin biopsy. The CBC and chemistry were within normal limits for all dogs. There were varying degrees of suppression of the hypothalamic-pituitary-adrenocortical (HPA) axis with difluprednate treatment. Dogs with the most profound alopecic changes had less pronounced HPA axis suppression compared to dogs with no integumentary changes. Skin biopsies demonstrated follicular atrophy and follicular keratosis. When topical difluprednate was reduced to unilateral therapy, the hair regrew on the untreated side of the face. In addition to the affected research dogs, a 7-year old female spayed Chihuahua that was being treated as a clinical patient with long-term difluprednate 0.05% ophthalmic emulsion developed generalized hypotrichosis on the head and body and a potbellied appearance. ACTH stimulation testing revealed suppression of the HPA axis with a mild increase in serum alkaline phosphatase (ALP) activity and a urine specific gravity of 1.016. The combination of clinical signs and laboratory abnormalities was supportive of iatrogenic hyperadrenocorticism. Conclusions In dogs long-term use of difluprednate ophthalmic emulsion results in HPA axis suppression and in some cases iatrogenic hyperadrenocorticism. A novel pattern of localized alopecia is suspected to be related to dermal absorption and local action due to superior potency and penetration compared to other commonly utilized ophthalmic corticosteroids. Keywords: Alopecia, Canine, Corticosteroids, Difluprednate (Durezol[R]), Follicular atrophy, Hypothalamic-pituitary-adrenocortical (HPA) axis, Ophthalmic</description><subject>Alopecia</subject><subject>Baldness</subject><subject>Causes of</subject><subject>Complications and side effects</subject><subject>Cushing syndrome</subject><subject>Difluprednate</subject><subject>Diseases</subject><subject>Dogs</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Health aspects</subject><subject>Hypothalamic-pituitary-adrenal axis</subject><subject>Ophthalmic drugs</subject><subject>Uveitis</subject><issn>1746-6148</issn><issn>1746-6148</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptTs1KAzEYDKJgrb6ApwXPqUk2m59jqVqFgpfey7dfkjaSbpbN9lCf3gU99CBzmGGYGYaQR84WnBv1XLiwXFMmOGU104LaKzLjWiqquDTXF_qW3JXyxZiUVqsZedlkhBS_vasg5d5jhAo6V5VT3w--lJi7KofqcO7zeIAEx4i0j-MpjjCcKbjBd5DuyU2AVPzDH8_J9u11u3qnm8_1x2q5oXulGdXOGNRcCulaCaFVaJmyquYowYUWRcC2aUwTeKPRWLAChdchGNsaJk1Tz8nT7-wekt_FLuRxADzGgrulMqq2tVBsSi3-SU1wfjqfOx_i5F8UfgCdHl2B</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Quantz, Katelin</creator><creator>Anderson, Amanda L</creator><creator>Harman, Christine D</creator><creator>Noland, Erica L</creator><creator>Del Valle, Jacquelyn M</creator><creator>Occelli, Laurence M</creator><creator>Burn, Jessica B</creator><creator>Petersen-Jones, Simon M</creator><creator>Langlois, Daniel K</creator><creator>Pirie, Chris G</creator><creator>Petersen, Annette D</creator><creator>Komáromy, András M</creator><general>BioMed Central Ltd</general><scope/></search><sort><creationdate>20211201</creationdate><title>Localized alopecia and suppression of hypothalamic-pituitary-adrenal</title><author>Quantz, Katelin ; Anderson, Amanda L ; Harman, Christine D ; Noland, Erica L ; Del Valle, Jacquelyn M ; Occelli, Laurence M ; Burn, Jessica B ; Petersen-Jones, Simon M ; Langlois, Daniel K ; Pirie, Chris G ; Petersen, Annette D ; Komáromy, András M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g670-7d88c71424db4afb6c9069631c4adfbc2fcb5585f157c89a92c2e7ff89b804853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alopecia</topic><topic>Baldness</topic><topic>Causes of</topic><topic>Complications and side effects</topic><topic>Cushing syndrome</topic><topic>Difluprednate</topic><topic>Diseases</topic><topic>Dogs</topic><topic>Dosage and administration</topic><topic>Drug therapy</topic><topic>Health aspects</topic><topic>Hypothalamic-pituitary-adrenal axis</topic><topic>Ophthalmic drugs</topic><topic>Uveitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quantz, Katelin</creatorcontrib><creatorcontrib>Anderson, Amanda L</creatorcontrib><creatorcontrib>Harman, Christine D</creatorcontrib><creatorcontrib>Noland, Erica L</creatorcontrib><creatorcontrib>Del Valle, Jacquelyn M</creatorcontrib><creatorcontrib>Occelli, Laurence M</creatorcontrib><creatorcontrib>Burn, Jessica B</creatorcontrib><creatorcontrib>Petersen-Jones, Simon M</creatorcontrib><creatorcontrib>Langlois, Daniel K</creatorcontrib><creatorcontrib>Pirie, Chris G</creatorcontrib><creatorcontrib>Petersen, Annette D</creatorcontrib><creatorcontrib>Komáromy, András M</creatorcontrib><jtitle>BMC veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quantz, Katelin</au><au>Anderson, Amanda L</au><au>Harman, Christine D</au><au>Noland, Erica L</au><au>Del Valle, Jacquelyn M</au><au>Occelli, Laurence M</au><au>Burn, Jessica B</au><au>Petersen-Jones, Simon M</au><au>Langlois, Daniel K</au><au>Pirie, Chris G</au><au>Petersen, Annette D</au><au>Komáromy, András M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localized alopecia and suppression of hypothalamic-pituitary-adrenal</atitle><jtitle>BMC veterinary research</jtitle><date>2021-12-01</date><risdate>2021</risdate><volume>17</volume><issue>1</issue><issn>1746-6148</issn><eissn>1746-6148</eissn><abstract>Background Despite the common use of topical ophthalmic corticosteroids in dogs, detailed reports on systemic and dermatologic adverse effects are limited. Results Nine purpose-bred research Beagles were treated with difluprednate 0.05% ophthalmic emulsion in one or both eyes 2-3 times daily. Some difluprednate treated dogs developed mild to severe alopecia of the periocular region, face, and distal pinna (5/9). The median duration of treatment prior to onset of dermatologic signs for difluprednate treated dogs was 550 days (453-1160 days). Diagnostic testing included complete blood count (CBC) and serum biochemistry, adrenocorticotropic hormone (ACTH) stimulation testing combined with endogenous ACTH measurement, and skin biopsy. The CBC and chemistry were within normal limits for all dogs. There were varying degrees of suppression of the hypothalamic-pituitary-adrenocortical (HPA) axis with difluprednate treatment. Dogs with the most profound alopecic changes had less pronounced HPA axis suppression compared to dogs with no integumentary changes. Skin biopsies demonstrated follicular atrophy and follicular keratosis. When topical difluprednate was reduced to unilateral therapy, the hair regrew on the untreated side of the face. In addition to the affected research dogs, a 7-year old female spayed Chihuahua that was being treated as a clinical patient with long-term difluprednate 0.05% ophthalmic emulsion developed generalized hypotrichosis on the head and body and a potbellied appearance. ACTH stimulation testing revealed suppression of the HPA axis with a mild increase in serum alkaline phosphatase (ALP) activity and a urine specific gravity of 1.016. The combination of clinical signs and laboratory abnormalities was supportive of iatrogenic hyperadrenocorticism. Conclusions In dogs long-term use of difluprednate ophthalmic emulsion results in HPA axis suppression and in some cases iatrogenic hyperadrenocorticism. A novel pattern of localized alopecia is suspected to be related to dermal absorption and local action due to superior potency and penetration compared to other commonly utilized ophthalmic corticosteroids. Keywords: Alopecia, Canine, Corticosteroids, Difluprednate (Durezol[R]), Follicular atrophy, Hypothalamic-pituitary-adrenocortical (HPA) axis, Ophthalmic</abstract><pub>BioMed Central Ltd</pub><doi>10.1186/s12917-021-03072-9</doi></addata></record> |
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subjects | Alopecia Baldness Causes of Complications and side effects Cushing syndrome Difluprednate Diseases Dogs Dosage and administration Drug therapy Health aspects Hypothalamic-pituitary-adrenal axis Ophthalmic drugs Uveitis |
title | Localized alopecia and suppression of hypothalamic-pituitary-adrenal |
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